Prostate cancer is a potentially debilitating illness that affects work, interpersonal relationships, and overall quality of life. Evidence has shown that if caught early, it can be treated effectively. Therefore, treating prostate cancer, whether by standard therapy or emerging treatments, can be beneficial to both healthcare professionals and their patients. This course will cover the epidemiology, diagnosis, screening, and pathophysiology of prostate cancer. It will also review the risks and benefits associated with screening. It discusses the potential role of diet in reducing the risk of prostate cancer. Different treatment regimens for prostate cancer, including surgery, radiotherapy, chemotherapy, androgen deprivation therapy, and 5-alpha reductase inhibitors, will be outlined.

Education Category: Men's Health
Release Date: 11/01/2013
Expiration Date: 10/31/2016


This intermediate course is designed for all certified psychologists involved in the care of clients with prostate cancer.

Accreditations & Approvals

NetCE is approved by the American Psychological Association to sponsor continuing education for psychologists. NetCE maintains responsibility for this program and its content.

Designations of Credit

NetCE designates this continuing education activity for 5 credit(s).

Course Objective

Although prostate cancer is the most common cancer diagnosed in men, it has a relatively good prognosis when diagnosed and treated early. The purpose of this course is to educate psychologists about the epidemiology, screening, diagnosis, and treatment of prostate cancer to ensure that clients receive the best possible care and are participants in their healthcare decisions.

Learning Objectives

Upon completion of this course, you should be able to:

  1. Review the epidemiology and demographics of prostate cancer.
  2. Discuss what is known about the pathophysiology of prostate cancer.
  3. Discuss the associated symptoms and diagnosis of prostate cancer.
  4. State the current recommendations regarding prostate cancer screening.
  5. Describe the potential role of diet in reducing prostate cancer risk.
  6. Discuss the role of surgery and radiotherapy as treatments for prostate cancer.
  7. Describe the role of androgen deprivation therapy for the treatment of prostate cancer.
  8. Discuss the role of chemotherapy as a treatment for prostate cancer.
  9. Analyze the research and use of 5-alpha reductase inhibitors as a treatment for prostate cancer.
  10. Recommend interventions for men who have experienced erectile dysfunction or depression as a result of prostate cancer, including considerations for non-English proficient patients.


John J. Whyte, MD, MPH, is currently the Chief Medical Expert and Vice President, Health and Medical Education at Discovery Channel, part of the media conglomerate Discovery Communications. In this role, Dr. Whyte develops, designs and delivers educational programming that appeals to both a medical and lay audience. This includes television shows, online content, and DVDs.

Prior to Discovery, Dr. Whyte was in the Immediate Office of the Director at the Agency for Healthcare Research Quality. He served as Medical Advisor/Director of the Council on Private Sector Initiatives to Improve the Safety, Security, and Quality of Healthcare. Prior to this assignment, Dr. Whyte was the Acting Director, Division of Medical Items and Devices in the Coverage and Analysis Group in the Centers for Medicare & Medicaid Services (CMS). CMS is the federal agency responsible for administering the Medicare and Medicaid programs. In his role at CMS, Dr.Whyte made recommendations as to whether or not the Medicare program should pay for certain procedures, equipment, or services. His division was responsible for durable medical equipment, orthotics/prosthetics, drugs/biologics/therapeutics, medical items, laboratory tests, and non-implantable devices. As Division Director as well as Medical Officer/Senior Advisor, Dr. Whyte was responsible for more national coverage decisions than any other CMS staff.

Dr. Whyte is a board-certified internist. He completed an internal medicine residency at Duke University Medical Center as well as earned a Master’s of Public Health (MPH) in Health Policy and Management at Harvard University School of Public Health. Prior to arriving in Washington, Dr. Whyte was a health services research fellow at Stanford and attending physician in the Department of Medicine. He has written extensively in the medical and lay press on health policy issues.

Faculty Disclosure

Contributing faculty, John J. Whyte, MD, MPH, has disclosed no relevant financial relationship with any product manufacturer or service provider mentioned.

Division Planner

William E. Frey, DDS, MS, FICD

Division Planner Disclosure

The division planner has disclosed no relevant financial relationship with any product manufacturer or service provider mentioned.

About the Sponsor

The purpose of NetCE is to provide challenging curricula to assist healthcare professionals to raise their levels of expertise while fulfilling their continuing education requirements, thereby improving the quality of healthcare.

Our contributing faculty members have taken care to ensure that the information and recommendations are accurate and compatible with the standards generally accepted at the time of publication. The publisher disclaims any liability, loss or damage incurred as a consequence, directly or indirectly, of the use and application of any of the contents. Participants are cautioned about the potential risk of using limited knowledge when integrating new techniques into practice.

Disclosure Statement

It is the policy of NetCE not to accept commercial support. Furthermore, commercial interests are prohibited from distributing or providing access to this activity to learners.

Table of Contents

Technical Requirements

Supported browsers for Windows include Microsoft Internet Explorer 9.0 and up, Mozilla Firefox 3.0 and up, Opera 9.0 and up, and Google Chrome. Supported browsers for Macintosh include Safari, Mozilla Firefox 3.0 and up, Opera 9.0 and up, and Google Chrome. Other operating systems and browsers that include complete implementations of ECMAScript edition 3 and CSS 2.0 may work, but are not supported.

#63881: Prostate Cancer

  • Back to Course Home
  • Participation Instructions


Prostate cancer is the most commonly diagnosed cancer in men, with more than 200,000 cases diagnosed annually in the United States alone [1]. It is a disease that has a high survival rate if diagnosed and treated early. However, many cases are not diagnosed until a later stage and thus may be at a lower survival rate.

As this cancer has a significant impact in society, much research has been performed in areas of diagnosis and treatment. Some of the developments have improved outcomes associated with early treatment and may potentially improve outcomes in advanced cases. Healthcare professionals may not be aware of the most recent advances related to prostate cancer.

This course will cover the epidemiology, diagnosis, screening, and pathophysiology of prostate cancer. It will also review the risks and benefits associated with screening and the potential role of diet in reducing the risk of prostate cancer. Different treatment regimens for prostate cancer, including surgery, radiotherapy, chemotherapy, androgen deprivation therapy (ADT), and 5-alpha reductase inhibitors, are discussed.


In the United States in 2013, new cases of prostate cancer (238,590) were projected to account for 28% of all cancers diagnosed in men [1]. Despite the advances in early detection and a decline in the death rate over the last decade, prostate cancer continues to cause substantial mortality in the United States. It ranked second among the 10 leading cancer-related causes of death for men in 2013; lung and bronchus cancer remained the number one cause [1]. The clinical incidence of prostate cancer in the United States has changed during the past several decades, increasing from less than 100 cases per age-adjusted 100,000 population in 1975 to a peak of 240 cases per 100,000 men in 1992, then fluctuating but declining (-1.9%) (averaging 175 cases per 100,000 men) between 2000 and 2009 [1].

One in every 6 American men will be diagnosed with prostate cancer at some point during his lifetime [1]. In the United States, most prostate cancer is diagnosed early and carries a good prognosis; 92% of men are diagnosed with local or regional disease, and the 5-year survival rate for localized or regional prostate cancer is 100% [3]. However, metastatic prostate cancer at the time of diagnosis has shown a 5-year survival rate as low as 30.6% [1,3].

The incidence of prostate cancer generally increases with age. According to one report of prostate cancer cases in the United States between 2002 and 2006, approximately 62% of cases were diagnosed in men 65 years of age or older [3]. Nearly 9% of cases were diagnosed in men between the ages of 45 and 54 years, a drastic increase from almost no cases in younger age groups [3]. Men 65 to 74 years of age represented the largest percentage of diagnosed cases (35.6%). In addition, 21.4% of cases were diagnosed in men 75 to 84 years of age, and roughly 5% of cases were found in men 85 years of age or older [3].

A study of autopsies by Yin and colleagues revealed an age-dependent increase in prostate cancer [7]. Among the study group, about 35% of men 60 to 69 years of age and 46% of men 70 to 81 years of age had prostate cancer [7]. The sample consisted of mainly white men with no history of intervention for prostatic disease. The United States will continue to see an increase in prostate cancer as the population ages and becomes more diverse [4,5,6].

In regards to race and ethnicity, African American men appear to be disproportionately affected [1,3]. A prospective study of heart disease and cancer among male healthcare professionals found an age-adjusted rate of prostate cancer that was 73% higher for African Americans compared to white men. The increased prostate cancer risk in African American men remained elevated even after adjusting for dietary and lifestyle risk factors [6]. African American men are also more likely to die of prostate cancer than white, Hispanic, or Asian men. The increased risk seen in the African American population is believed to be multifactorial, caused by alterations in an individual's environment (e.g., diet, exposure to toxins), participation in screening, genetic background, and physiologic status (e.g., sex steroid hormone levels) [5,8]. The Surveillance, Epidemiology, and End Results (SEER) study's age-adjusted data confirmed the differences in race/ethnic populations. The incidence of prostate cancer is greatest in African Americans, lower in white and Hispanic/Latino populations, and least in Asian American/Pacific Islanders and Native American/Alaska Natives [1,3].

It is interesting to note that men diagnosed with prostate cancer have higher rates of non-cancer-related mortality than men in the general population [9]. Some of this excess mortality may be attributed to treatment, such as ADT, that is used for metastatic disease [10]. Because prostate cancer that is detected and treated early has a favorable prognosis, selection of treatments is particularly important. In fact, unwanted effects of treatments (e.g., adverse effects, complications) may have a greater negative impact on overall health and quality of life than the prostate cancer itself.


Almost all cases of prostate cancer are adenocarcinoma [11,12]. According to most studies, about 4% of prostate cancer cases exhibit transitional cell morphology and may originate in the urogenital lining of the prostatic urethra [13]. A few cases of prostate cancer have neuroendocrine morphology, originating either in neuroendocrine stem cells normally present in the prostate or as a result of aberrant cell transformation whereby benign prostatic hyperplasia (BPH) develops [13].

The prostate gland consists of the prostate capsule and four zones. The transition zone typically constitutes about 5% to 10% of the glandular volume of the prostate and surrounds the urethra at the point that the ejaculatory ducts enter the gland [11,14]. The central zone surrounds the transition zone and accounts for approximately 20% to 25% of the mass of the normal glandular prostate [11,14]. The ejaculatory ducts pass through the central zone before entering the urethra [11]. The peripheral zone makes up about 75% of the prostatic volume in healthy adult males. It is a double row of duct buds that laterally surround the central zone, and it occupies the region of the prostate closest to the rectum [11,14]. The anterior zone is nonglandular (primarily made of fibromuscular tissue) and constitutes about one-third of the mass within the prostatic capsule. It is an intermingled region, with fibers descending from the bladder neck and urethral sphincter [11]. It is the portion of the prostate closest to the abdomen.

Most prostate cancer cases (about 70%) originate in the peripheral zone [11,13,14]. The rest develop in the transitional zone (10% to 15%) and in the central zone (15% to 20%) [13]. Most men have clinically localized disease at diagnosis. The majority of cases are multifocal (i.e., multiple separate malignant groups). These multicentric lesions are often present in different zones of the prostate and typically are of different grades [15].

Testosterone is the main circulating androgen in men and is a significant factor involved in the physiological development of prostate cancer [16,17]. In the prostate and other organs, testosterone functions as a prohormone. The prostatic stromal and basal cells convert testosterone to dihydrotestosterone (DHT) [19]. This process is caused by 5-alpha reductase (5AR), an intracellular enzyme present in the prostate, skin, and liver [19]. The ratio of testosterone to DHT in blood samples is approximately 10:1, but this ratio is reversed in the prostate [18].


Prostate cancer does not usually show symptoms until an advanced stage. However, the disease can be detected in asymptomatic men who have focal nodules in the prostate on a digital rectal examination (DRE) [20,21]. As a result, there has been movement in the past several decades to expand prostate cancer screening in asymptomatic populations [22,37]. Despite the resulting increase in early detections/diagnoses, the benefits versus the harms of aggressive detection and treatment have been re-evaluated, and screening for prostate cancer, especially in average-risk groups, is generally no longer recommended or is explicitly discouraged. In patients with more advanced presentation, there can be urinary retention and neurologic symptoms resulting from epidural metastases and cord compression [23]. Screening and assessment is usually recommended for patients with signs of prostate disease.


Prostate-specific antigen (PSA) is a serine protease that liquefies the seminal fluid. Although it is found in a much greater concentration in seminal fluid, it can also be measured in serum. It is considered a more readily available and less invasive test for both screening and management of prostate cancer [22]. Unfortunately, PSA levels can also be elevated in benign prostatic conditions, such as BPH and prostatitis, leading to false-positive readings [22,24]. In fact, inflammation itself may play a role in the pathogenesis of prostate cancer, making it difficult to exclude any relationship between prostate cancer and a palpable abnormality in another neighboring area [25].

Newer definitions of an abnormal PSA level have also been debated. Lower PSA thresholds are used now to recommend biopsy, with a corresponding increase in the number of men undergoing biopsy and the number of cancers found in men with low PSA levels [26]. A PSA level greater than 4.0 ng/mL is considered abnormal. However, a value of greater than 2.6 ng/mL has been advocated for the detection of small, organ-confined tumors [27].

When PSA levels are found to be outside of normal limits, the free PSA (fPSA) test is recommended before biopsy [37,147]. Biopsy is associated with significant burden and harm (e.g., pain, urinary tract infection, hospitalization). The test measures the percentage of free PSA relative to PSA and is expressed as %fPSA, with a lower number indicating increased cancer risk. A man with a %fPSA greater than 25 has an 8% chance of having prostate cancer, while there is a 56% chance he will have prostate cancer when %fPSA is less than 10. The fPSA test is noninvasive and has a 95% specificity for detecting cancer in men with %fPSA less than 10 [147].


Tumor aggressiveness can be determined by a pathologist's examination of the microscopic pattern of the cancer cells. The most commonly used tumor grading system is the Gleason grading [28]. This system assigns a grade for each prostate cancer from 1 (least aggressive) to 5 (most aggressive) based on the degree of architectural differentiation of the tumor. The Gleason score is obtained by assigning a primary grade to the most predominant grade present and a secondary grade to the second most predominant grade [28].

The standard T (extent of local tumor), N (status of regional lymph nodes), and M (distant metastasis) system has been used to stage prostate cancer tumors (Table 1) [29,124]. The TNM staging for prostate cancer also includes a category for histopathological grade (G), which takes into consideration the Gleason grading score. After each of the four categories has been graded, the cancer may be assigned a stage [124].


Tumor (T)
TXPrimary tumor cannot be assessed
T0No evidence of primary tumor
T1Clinically inapparent tumor not palpable nor visible by imaginga: Tumor incidental histologic finding in 5% or less of tissue resected
b: Tumor incidental histologic finding in more than 5% of tissue resected
c: Tumor identified by needle biopsy (e.g., because of elevated PSA)
T2Tumor confined within prostateaa: Tumor involves 50% or less of one lobe
b: Tumor involves more than 50% of one lobe but not both lobes
c: Tumor involves both lobes
T3Tumor extends through the prostate capsuleba: Extracapsular extension (unilateral or bilateral)
b: Tumor invades seminal vesicle(s)
T4Tumor is fixed or invades adjacent structures other than seminal vesicles (e.g., bladder neck, external sphincter, rectum, levator muscles, and/or pelvic wall)
Regional Lymph Nodes (N)
NXRegional lymph nodes were not assessed
N0No regional lymph node metastasis
N1Metastasis in regional lymph node(s)
Distant Metastases (M)
MXDistant metastasis cannot be assessed (not evaluated by any modality)
M0No distant metastasis
M1Distant metastasisa: Nonregional lymph node(s)
b: Bone(s)
c: Other site(s) with or without bone disease
Histopathic Grade (G)
GXGrade cannot be assessed
G1Well differentiated (slight anaplasia) (Gleason score of 2–4)
G2Moderately differentiated (moderate anaplasia) (Gleason score of 5–6)
G3-4Poorly differentiated or undifferentiated (marked anaplasia) (Gleason score of 7–10)

a Tumor that is found in one or both lobes by needle biopsy but is not palpable or reliably visible by imaging is classified as T1c.

b Invasion into the prostatic apex or into (but not beyond) the prostatic capsule is classified as T2 not T3.


Patient risk stratification schemes have been developed by the American Urology Association (AUA) based on the PSA level, biopsy Gleason score, and American Journal of Cancer Care (AJCC) clinical T-category. The cancer is graded based on the risk of PSA failure and prostate-cancer-specific mortality following radical prostatectomy, external beam radiotherapy, or interstitial prostate brachytherapy [30]:

  • Low risk: PSA ≤10 ng/mL, a Gleason score of 6 or less, and clinical stage T1c or T2a

  • Intermediate risk: PSA >10 to 20 ng/mL, or a Gleason score of 7, or clinical stage T2b but not qualifying for high risk

  • High risk: PSA >20 ng/mL, or a Gleason score of 8 to 10, or clinical stage T2c

Expectant management, historically termed watchful waiting, is generally reserved in older men with limited life expectancy, offering hormonal therapy at the time of disease progression. However, the impact of age on the treatment effect of radical prostatectomy, independent of life expectancy, remains unclear. Thus, another management strategy concept, active surveillance, has been introduced. This strategy identifies prostate cancer progression signs and the patient is treated accordingly; it is an effective option for low-risk cancers. As opposed to watchful waiting, active surveillance allows for men with features of low-risk disease to defer (rather than reject) prostate cancer therapy and any related morbidity [31].


Before the discovery of PSA, DRE was the primary tool used to screen for prostate cancer [22,25]. A positive DRE was followed by biopsy. Findings suggesting cancer or obstructive symptoms then led to transurethral resection of the prostate (TURP). However, a prostate tumor must reach a significant size to be palpable, and as with PSA, false-positive tests can also occur with DRE. Furthermore, prostate cancer is not always detected in the same area of the prostate with suspicious findings on DRE [32].

Thus, other tests were needed to assist in prostate cancer diagnosis, and the PSA appeared to fill that need. As early as the late 1980s, physicians in the United States began to analyze PSA levels in men who did not have prostate cancer but were considered at high risk of having the disease (i.e., most men older than 50 years of age) [26]. In 1986, the U.S. Food and Drug Administration (FDA) approved the PSA test to monitor the disease status in prostate cancer patients [26]. In 1994, the FDA approved PSA for use as an aid in the early detection of prostate cancer. In the United States, the use of the PSA test in white men reached an annual rate of 38% in 1995 and remained at this percentage [33]. In 1996, a PSA test preceded 83% of the prostate cancer diagnoses in white patients and 77% in African American patients [33]. The literature has shown that PSA and DRE are best used in a complementary fashion [21]. Evidence has shown that prostate cancers detected either by PSA or DRE alone have more favorable pathological characteristics than those found due to abnormalities in both PSA and DRE [21].


Available screening methods and enhanced awareness has led to an increased number of men in whom prostate cancer is diagnosed at an earlier stage. The primary benefit of screening is a lower stage and grade of cancer at the time of diagnosis, and the high rate of localized disease at the time of diagnosis (92% to 96%) reflects, in part, the increased number of cancers that are detected earlier through screening [38,150,151]. Despite this benefit, an effect of screening on mortality has not been demonstrated. The National Cancer Institute's Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial was a U.S.-based randomized trial with enrollment from 1993–2001, involving 76,693 men at 10 study centers. After 13 years of follow-up in the PLCO trial, there was no benefit of annual screening on mortality [49]. A meta-analysis (five randomized controlled trials) similarly demonstrated no effect of screening on prostate cancer-specific or overall mortality [152].

In addition to a lack of effect on mortality, screening is associated with high rates of false-positive results, overdiagnosis and subsequent overtreatment, and complications. Among men who have had four PSA tests, the cumulative risk for at least one false-positive result is 12.9% [150]. Rates of overdiagnosis have been estimated at 17% to 50%, and 23% to 42% of all screen-detected prostate cancers are overtreated [150,153]. Furthermore, treatment is associated with complication rates of 20% to 50% [39,150]. These findings have led expert panels to update their screening recommendations (Table 2) [34,35,36,37,38,39,149].


OrganizationYear of PublicationRecommendationNotes
American Urological Association2013No routine screening

Decisions should be individualized for men younger than 55 years who are at high risk.

Shared decision-making should take place for men 55 to 69 years of age, for whom screening is of greatest benefit.

American College of Physicians2013No routine screening with PSA for average-risk men younger than 50 years of age, men older than 69 years of age, or men with a life expectancy of less than 10 to 15 years
U.S. Preventive Services Task Force2012Recommends against routine prostate cancer screening.Community- and employer-based screening should be discontinued. Physicians who continue to offer screening are obligated to engage in shared decision-making that reflects an explicit understanding of the possible benefits and harms and to respect patients' preferences.
American Society of Clinical Oncology2012Discourages general screening for men with a life expectancy of ≤10 years, as the harms outweigh the benefitsDiscuss the individual appropriateness of screening with men who have a life expectancy >10 years.
National Comprehensive Cancer Network2012

Primarily addresses process in men who choose to be screened.

Consider obtaining a baseline PSA at 40 years of age due to increased risk if PSA is above the median for a patient's age group. PSA should not replace DRE.

American Cancer Society2010No routine screeningDiscuss potential benefits and limitations of prostate cancer early detection at specified ages. Men should choose to be screened only after they receive information about the uncertainties, risks, and potential benefits associated with prostate cancer screening.
American College of Preventive Medicine2008Insufficient evidence to recommend routine population screening with DRE and PSA.Give men information about potential benefits and harms of screening, including limits of current evidence, and allow them to make their own decision. Discussion should be done annually. "Usual age" for screening is 50 to 70 years in average-risk men. Effectiveness is questionable in men with life expectancy <10 years. More information is needed regarding possible benefit of screening high-risk men at younger ages.

Overall, experts recommend against routine screening for most men and emphasize the need to consider life expectancy and the patient's age and risk factors for the disease. The age to start a discussion about screening varies slightly among the guidelines. For example, the American Urological Association (AUA) and the American Cancer Society (ACS) do not recommend routine screening for men of any age [2,39]. Instead, the ACS advises that patients with greater than a 10-year life expectancy make an informed decision whether to be screened after discussing the uncertainties, risk, and potential benefits of screening with their healthcare provider. The ACS early detection guideline suggests the information with which to make a decision should be provided to men at various ages based on risk level [2]:

  • Age 50: Men at average risk

  • Age 45: Men at higher risk (e.g., black race with a first-degree relative diagnosed with prostate cancer before 65 years of age)

  • Age 40: High-risk populations (e.g., multiple family members diagnosed with prostate cancer before 65 years of age)

The AUA panel recommends that the screening decision be based on individual risk and on the patient's personal values and preferences regarding early detection [39]. The AUA notes that the benefit of screening is greatest for men 55 to 69 years of age; routine PSA screening in men 70 years of age or older and men with a life expectancy less than 10 to 15 years is not recommended. In contrast, the U.S. Preventive Services Task Force (USPSTF) explicitly recommends against PSA-based screening for men of any age [36,148].

In spite of these conflicting guidelines, many physicians believe that healthy men should be offered the opportunity for prostate cancer screening [22]. As prostate cancer is rare for men younger than 40 years of age, screening is not typically initiated until at least the fifth decade [7]. However, baseline PSA measurements at a young age can be useful to predict the risk of ever developing prostate cancer; a measurement at 40 years of age may be useful to create a personalized risk profile and avoid missing signs of prostate cancer diagnosis [22,34].

Every medical intervention, whether it is therapeutic or diagnostic, does have risk. Table 3 summarizes some of the risks associated with prostate cancer screening.


False positive incidence
Discomfort of biopsy
False reassurance
Results may not be accurate
Unnecessary treatment of indolent disease
More harm than benefit with disease
Psychological harm
Men with false-positive readings may worry more about prostate cancer
Risk of significant bleeding, infection

The European Randomized Study of Screening for Prostate Cancer followed 182,000 men from 7 European countries, 50 to 74 years of age. The "core" age group used for analysis was 55 to 69 years, which accounted for 162,243 subjects. The average follow-up was 8.8 years. Participants were randomized to PSA screening (on average, once every 4 years) or no screening. In most centers, the cutoff was 3.0 ng/mL. Compliance in the screening group was 82% for at least one test. Overall, 16.2% of tests were positive, and compliance with biopsy recommendations was 85.8%. However, 75.9% of biopsies showed that the PSA was a false positive [50]. The cumulative incidence of prostate cancer was 8.2% in the screening group and 4.8% in controls. In intention-to-screen analysis, death from prostate cancer was lower in the screening group. Absolute risk difference was 0.71 death/1,000 men. By intention-to-screen analysis, to prevent one death 1,410 men would need to be screened and 48 additional cases treated. Including only men who were actually screened, 1,068 men would need to be screened and 48 treated to prevent one death [50].

Researchers continue to investigate ways to make screening more effective. Using a higher PSA threshold for biopsy for older men and less frequent screening for men with low PSA levels are strategies that may reduce the risk of overdiagnosis as well as prostate cancer-related mortality [154].

Informed decision making is integral in selecting approaches to screening, with every guideline emphasizing the need to discuss the potential benefits, harms, and limitations associated with screening with their male patients. The ACS notes that men should receive information about screening directly from their healthcare provider or be referred to reliable and "culturally appropriate" sources [38]. Decision aids can be especially useful in helping men and their healthcare providers weigh the benefits and risks of screening, and studies of decision aids have led to improved knowledge and have increased men's desire for an active role in decision making [38,39,155]. The National Comprehensive Cancer Network (NCCN) guideline offers talking points for discussion, and the American Society of Clinical Oncology provides a decision aid tool (http://stage.asco.org/sites/default/files/psa_pco_decision_aid_71612.pdf).

Despite the continued emphasis on informed decision making, the percentage of men who report having had a discussion with their healthcare providers about screening has been suboptimal, with a rate of about 63% to 66% of the general male population [156,157]. Black men were most likely to have had a discussion, and men without a usual source of care were the least likely [157].

For men who choose to have screening for prostate cancer, the combination of DRE and PSA is the preferred method, providing better predictive value than either method alone [150]. The sensitivity of PSA testing is higher than that of DRE, especially for tumors that are more aggressive [151]. However, the PSA level can vary as a result of several factors.


Multiple factors should be taken into account before proceeding to biopsy, including PSA and DRE results, free/total PSA, PSA velocity, PSA density, family history, ethnicity, prior biopsy history, and comorbidities.

Before 1989, most non-TURP prostate biopsies were obtained by directed needle biopsy of palpably abnormal nodules in the gland [45]. Since then, spring-loaded biopsy devices using small-bore (18-gauge) needles, in combination with transrectal ultrasonography (TRUS), have led to random systematic sextant ultrasound-guided transrectal biopsies of the prostate [46]. This procedure was quickly adopted as the method of choice for obtaining tissue from patients with suspected prostate cancer [47]. However, it became apparent that the widely adopted sextant protocol did not detect as many cancer cases as a more extensive biopsy procedure. In one study, the cancer detection rate was 30% for a 6-core biopsy and 49% for a 12-core biopsy in patients with a PSA level of 4.1–10 ng/mL [48]. Today, urologists routinely take 10 to 14 cores per biopsy session. For patients with previously negative biopsy findings and a persistently elevated PSA level, saturation biopsies consisting of more than 30 biopsy cores have been advocated by some physicians, pushing to a new limit in the search for small foci of cancer [48].

Prostate cancer is found in about 25% of biopsy specimens, illustrating a problem regarding a well-defined threshold at which to obtain a biopsy specimen [44]. Although most cancer is detected with use of a PSA threshold of 4 ng/mL, some studies have shown that prostate cancer is subsequently found in men with levels in the range of 2.5–4.0 ng/mL [34]. These findings led the NCCN to suggest considering biopsy for men with a PSA level in the range of 2.6–4.0 ng/mL [166,167]. A positive DRE, regardless of PSA results, should prompt a biopsy [34].


There are more than 100 prostate cancer risk calculators developed to aid in screening decisions and treatment planning, most of which have undergone some form of validation [160]. Many are used clinically; however, their effectiveness continues to be debated. One reason uncertainty exists is that the same data set used to create the prediction models is typically used to validate them [159]. Thus, true validation may not exist for most of the available risk calculators, and even when independent data is used, flaws remain (e.g., poor calibration/discrimination) that have the potential to cause harm to a significant number of patients. Despite these facts, it is believed that prediction models are superior to conventional decision making based on PSA screening and DRE, particularly for the detection of patients at risk for aggressive, high-grade cancers [158,161,162].

The Prostate Cancer Prevention Trial Prostate Cancer Risk Calculator (PCPTRC) uses race, age, PSA, family history, DRE, prior biopsy information, and finasteride status to assign a risk level [51]. The tool was developed using data derived from the 5,519 men in the placebo group of the PCPT, and its efficacy was validated in a separate study [158]. The PCPTRC may be accessed online at http://deb.uthscsa.edu/URORiskCalc/Pages/uroriskcalc.jsp.

The Sunnybrook Prostate Risk Calculator (SPRC) focuses more on PSA levels to predict individual prostate cancer risk [52]. The calculator incorporates PSA, the free:total PSA ratio, ethnic background, family history, and DRE. According to the researchers, the Sunnybrook Prostate Risk Calculator is more accurate than conventional screening. Validation using an independent data set has been performed [158]. The tool may be accessed online at http://sunnybrook.ca/content/?page=occ-prostatecalc.

The Carcinoma of the Prostate (CaP) Calculator is available to both clinicians and patients in order to identify patients at increased risk and support an informed discussion about the disease and potential treatment options [53]. Based on peer-reviewed articles providing risk assessment tools, the CaP Calculator uses a number of factors in its calculation, including clinical T stage, Gleason score, pretreatment PSA, and core biopsy findings, if available. It gives multiple estimates of pathologic findings, PSA outcome after radical prostatectomy and radiation therapy, and clinical outcomes after radiation therapy. Additional research is necessary in order to independently validate use of the tool in making treatment and screening decisions. The CaP Calculator is available online at http://www.capcalculator.org.

A multi-institutional, 2130-patient study aimed at validating the SPRC (and to a lesser extent, the PCPTRC) examined how using these models influenced decisions regarding the use of biopsy [158,159]. Researchers found that neither calculator added clinical benefit for risk thresholds of less than 30%; although, in the authors' opinion, the SPRC performed better [158]. A comment on this study by Vickers emphasized that caution should be taken when using prediction modeling [159]. He asserts that although it has better discrimination than the PCPTRC, the Sunnybrook Calculator would also cause more harm than good for men with average risk, as it slightly underestimates risk (when risk is low), resulting in a lower use of biopsy based on a false low risk-profile [159].



There have been studies indicating that diet may impact both the development of prostate cancer and the aggressiveness of tumors [25,54]. However, determining a causal relationship between individual foods and nutrients and prostate cancer is not simple. It is generally believed that dietary associations are modified by genetic sensitivity [55,56]. Chan and colleagues concluded that consuming a diet of a wide variety of plant-based foods (cruciferous vegetables) and fish may prevent prostate cancer; more controlled evidence is still needed regarding specific dietary components [54].

Carmody and colleagues conducted a randomized trial of an intervention of men with recurrent prostate cancer changing to a primarily plant- and fish-based diet and assessed the affect of the change on their quality of life and rate of PSA increase [57]. The clinical trial faced multiple challenges, as only a minority of prostate cancer survivors adhered to the ACS recommended diet of five servings of fruit and vegetables daily [58]. This challenge in adherence was found to be a barrier to improved treatment outcomes.

Crawford and colleagues also noted some correlation between diet and rates of prostate cancer [4]. This relationship was seen previously in studies showing prostate cancer incidence increased considerably in Japanese men who immigrated to the United States [59]. However, subsequent studies showed inconclusive results. For example, the Cancer Prevention Study II Nutrition Cohort found an association between higher total red meat intake and an increased risk of prostate cancer in African American men but not in white men [60]. However, these results were not duplicated by the Multiethnic Cohort Study, which failed to identify an association between fat/meat intake and prostate cancer risk in any of the four racial/ethnic groups studied (African Americans, Japanese Americans, Hispanics, and whites) [61].

The Selenium and Vitamin E Cancer Prevention Trial (SELECT) is the largest-ever prostate cancer prevention trial. Its focus is to determine the validity of previous studies suggesting that selenium and vitamin E (alone or in combination) might reduce the risk of developing prostate cancer by 60% and 30%, respectively [53,62]. However, study data from the SELECT trial (ongoing) is not promising; supplemental selenium (200 µg/day) and vitamin E (400 IU/day), taken either alone or together for 7 to 12 years, did not decrease the risk of developing prostate cancer [63]. The data also show two concerning trends: a significant increase in the number of prostate cancer cases in men taking only vitamin E and slight increases in the number of cases in men taking only selenium and selenium/vitamin E combined [63]. The absolute increase in risk of prostate cancer per 1000 person-years was 1.6 for vitamin E, 0.8 for selenium, and 0.4 for the combination.

Linking diet to the risk of prostate cancer, however, remains an intriguing topic for future research, and other studies have focused on nutritional links. Gao and colleagues found a relationship between increased calcium intake and a possible increased risk of prostate cancer [64]. According to their meta-analysis from prospective studies, the relative risk of prostate cancer was more likely in men with the highest intake of dairy products and calcium compared with men with the lowest intake; however, the apparent intake was small [64]. Building on research indicating that higher dairy milk intake may be associated with increased incidence of prostate cancer, a large cohort study of the Physicians' Health Study (n=21,660) found that whole milk intake, specifically, was associated with fatal disease and progression to fatal disease after diagnosis, whereas nonfat/lowfat milk was associated with a greater risk of nonaggressive disease but not death [163]. A separate 2010 animal study concluded that a Western diet (i.e., high in fat and cholesterol) increased prostate tumor incidence, grade, and burden [164].

Yan and colleagues, based on meta-analysis of cohort and case-control studies, found a possible protective effect from the ingestion of soy products [65]. The cause of this decreased risk is not clearly known, but it is theorized to be either caused by an estrogenic effect or the inhibition of 5AR [65]. Giovannucci and colleagues investigated the link between tomato products and lycopene and the risk of prostate cancer [66]. While there was a potential protective effect, there was not sufficient evidence to support a health claim [66,67]. Other studies have investigated animal fats and vitamin D; some studies have shown a link between increases in both animal fat consumption and prostate cancer incidence, while other studies have not [68]. Meanwhile, some studies have investigated whether vitamin D analogs have a potential role in prostate cancer therapy [69].


There have been investigations into the role for aspirin and nonsteroidal anti-inflammatory drugs (NSAIDs) in the prevention of prostate cancer. The rationale of the role of aspirin and NSAIDs in prostate cancer prevention is most likely related to elevated prostaglandins and upregulation of cyclooxygenase-2 (COX-2) found in prostate cancer cell lines [70,71]. Two significant studies have focused on epidemiological evidence related to this potential approach [70,71].

Jacobs and colleagues discovered that, in the ACS Cancer Prevention Study II Nutrition Cohort, ingesting 30 or more pills per month over 5 or more years (either adult-strength aspirin or NSAIDs) was associated with a lower risk of prostate cancer [70]. Meanwhile, a meta-analysis of observational epidemiological studies by Mahmud and colleagues found the epidemiologic evidence for a protective effect of aspirin and NSAID use against prostate cancer to be suggestive but not conclusive [71]. While both of these studies were promising, more information is needed related to reduction in PSA levels and the effect on PSA sensitivity.


The three options for early-stage/low-risk prostate cancer include surgery, radiation therapy (either external beam radiation or radioactive tumor seeding [brachytherapy]), and active surveillance, also known as expectant management or watchful waiting [77]. However, the last option is not treatment in itself; it is actually a form of close patient management. Presently, there is no effective systemic therapy for early-stage prostate cancer.

There have also been other treatments investigated for more advanced prostate cancer, such as ADT and chemotherapy [10]. ADT is for prostate cancer patients who are hormone-sensitive, while chemotherapy is reserved primarily for the treatment of men with advanced or recurrent prostate cancer that does not respond to hormone therapy [10,73,74]. There are promising findings but, as with the early-stage type, no effective systemic therapies for the treatment of late-stage prostate cancer exist.

Other experimental modalities are being studied for use in the treatment of prostate cancer, including high-intensity focused ultrasound (HIFU). HIFU, which consists of ablating the tumor prostate with focused ultrasound waves via the endorectal probe, has shown some promise for patients with localized (early-stage) disease [143,144]. However, some studies have reported significant adverse effects, and additional research is necessary before it can be incorporated into treatment recommendations [145].


Before a radical prostatectomy is considered, physicians should ensure the disease is contained within the prostate gland. If so, there is a higher likelihood that surgery will be successful. A radical prostatectomy is a procedure whereby the prostate gland and the seminal vesicles are completely removed. Usually, this surgical procedure is performed in younger patients (40 to 60 years of age) with no metastases, as they have a greater chance of prostate-cancer-related death than older patients (70 to 90 years of age) [55]. Surgery has been widely documented to reduce mortality and rates of metastases in prostate cancer patients [55,75].

There are several surgical options when completing a prostatectomy [76]. The first option is either retropubic or perineal prostatectomy. With the retropubic procedure, the surgeon makes an incision in the abdomen to reach the prostate and may also remove nearby lymph nodes as a precautionary measure to prevent spread of disease [75]. The second option is a perineal prostatectomy, in which the surgeon makes an incision in the perineum; another abdominal incision is needed to remove lymph nodes [76]. In some hospitals, surgeons may do a laparoscopic prostatectomy, whereby instruments are passed through a few small incisions. While the laparoscopic procedure is generally associated with fewer complications and faster recovery, it is technically challenging and not always appropriate for removing all prostate tumors [76].

Cancer that has spread to lymph nodes signals the likelihood of more extensive disease that is less likely to be cured by surgery. This knowledge is vital when determining a treatment plan, so a pelvic lymphadenectomy is often completed prior to prostatectomy to check for prostate cancer spread [72]. The removed nodes are examined by a pathologist for evidence of cancer cells. If the nodes display evidence of cancer, radical prostatectomy would usually be excluded as a treatment option [72].


Some treatment centers also perform cryosurgery. This is a technique whereby prostate tissue is ablated by alternate freezing and thawing. It can be an outpatient procedure. The experience with this type of surgery for prostate cancer is limited, as there has been little published data documenting the effect of cryosurgery on metastasis-free, prostate-cancer-specific, or overall survival [79]. The 5-year biochemical disease-free survival rates have ranged from 48% to 92%, depending on the risk of recurrence, but long-term data on prostate cancer-specific survival are not yet available and there are no clearly defined guidelines for patient selection for cryosurgery as a salvage procedure [78]. However, the AUA notes that primary cryosurgery is an option for men with organ-specific disease without metastases [78]. Poorer outcomes after cryosurgery were noted for patients with larger prostates, as it is more difficult to uniformly freeze larger areas. A 2013 review of literature from 1980 to 2013 noted that this form of treatment has greatly improved over time, with biochemical disease-free survival rates now comparable to other treatment modalities [168]. Treatment-related morbidities have also decreased. Adjuvant ADT should be considered for men with clinical stage T3 prostate cancer [169].

Cryotherapy is a good option for eligible patients who cannot undergo radical prostatectomy due to comorbidities, obesity, or history of pelvic surgery [78]. Salvage cryotherapy may be beneficial for men with locally recurrent disease, a PSA less than 4 ng/mL, and no metastases for whom radiotherapy was not effective [78]. It is important to note that serious toxic effects have been noted with cryosurgery, including bladder outlet injury, urinary incontinence, sexual impotence, and rectal injury [77].


Radiotherapy is an option for cancer confined to the prostate and/or local tissues [10,72,77,80]. A randomized trial of external-beam radiation for prostate cancer found that long-term adjuvant treatment with ADT (gonadotropin-releasing hormone [GnRH] agonist) was associated with greater noncancer mortality than short-term therapy [81]. Another observational study of primary brachytherapy in men with early-stage prostate cancer found that men who received brachytherapy and short-term hormonal therapy had worse overall survival rates than men who did not receive such therapy, but there were no differences in prostate cancer-specific survival [82].

In addition, published retrospective series have shown adjuvant radiotherapy to reduce the risk of biochemical failure while improving local and distant disease control [83,84,85]. Biochemical failure is defined as three consecutive measurements of an increase of PSA greater than 2 ng/mL compared to the lowest pretreatment level. Three randomized trials comparing treatment with adjuvant radiotherapy to observation (active surveillance) in men with pathologic stage T3 or margin-positive disease showed a significant improvement in biochemical-failure-free survival in the radiotherapy group [83,84,85]. In spite of these promising outcomes, no effect on overall survival has been reported [80].

There has been no accepted optimal dose of radiotherapy as an adjuvant treatment for prostate cancer in spite of its use in the postoperative period. Reported doses have varied between 45 Gray (Gy) to 79 Gy, although most investigators have advocated a cumulative dose greater than 60 Gy [83,84,85]. According to the National Cancer Institute, greater improvements have been shown with higher doses of radiation (78–79 Gy) compared to conventional doses [77]. A treatment guideline published by the Working Group of the Clinical Practice Guideline on Prostate Cancer Treatment recommends the following dose schedule [170]:

  • 72–74 Gy in patients with clinically localized prostate cancer at low risk (cT1–cT2a, Gleason <7, and PSA ≤10 ng/mL)

  • 76–78 Gy in patients with clinically localized prostate cancer at intermediate risk (cT2b or Gleason =7 or PSA >10 ng/mL and ≤20 ng/mL)

  • At least 78 Gy in patients with clinically localized prostate cancer at high risk (T2c or Gleason >7 or PSA >20 ng/mL) or with prostate cancer at the locally advanced clinical stage (cT3)

Despite the lack of an identified optimal dose, radiotherapy has shown a significant benefit for prostate cancer therapy. Anscher and colleagues reported an improved rate of localized disease control with the addition of radiotherapy after prostatectomy; the 10-year local control rate was 92% with the addition of radiotherapy compared to 60% with observation alone [83]. In addition, Leibovich and colleagues reported that subjects who received adjuvant radiotherapy experienced no local or distance recurrence in men compared to a 16% rate of recurrence with observation alone [86]. Studies completed prior to the regular assessment of PSA levels have indicated significantly improved local disease control with adjuvant radiotherapy [87,88]. For example, a phase III study of adjuvant radiotherapy in men with stage T3 disease and a primary endpoint of metastasis-free survival found the 10-year rate favored adjuvant radiotherapy to observation alone; however, the difference was not significant [89]. Macdonald and colleagues noted their 5-year rate of freedom from both local recurrence and distant metastasis with adjuvant radiotherapy treatment was significant, at respective rates of 95% and 97%, indicating that radiotherapy has a demonstrated benefit for many prostate cancer patients [80].

Three large, randomized studies of radiotherapy compared with observation after surgery for pathologic stage T3 disease revealed a significant improvement in biochemical-failure-free survival after adjuvant therapy [89,90,91]. A European series trial by Bolla and colleagues reported improvements in biochemical survival and local control with radiotherapy [90]. Thompson and colleagues reported significant benefits in both PSA-free (>0.4 ng/mL) and relapse-free survival in men receiving adjuvant radiotherapy (60–64 Gy) [89]. Wiegel and colleagues reported an increase in the 4-year rate of biochemical-failure-free survival of 81% for radiotherapy-treated men compared with 60% in the control group [91]. However, Macdonald and colleagues analyzed the results with caution, recognizing that none of the men in their series had disease as advanced as those included in the other randomized trials [80,89,90,91].

The most common form of external-beam radiation for prostate cancer is intensity-modulated radiation therapy (IMRT), which allows the greatest concentration of radiation to be more finely focused. In one large study comparing IMRT with conformal radiation therapy and proton therapy, IMRT was associated with a lower rate of gastrointestinal morbidity and fewer hip fractures [172]. Patients who underwent IMRT were also less likely to require additional cancer therapies than those who received conformal radiation therapy.

Other radiation techniques, including proton-beam therapy and cyber knife, are being studied for use in the treatment of prostate cancer. In particular, the National Cancer Institute has noted that incorporating proton therapy is an attractive option, but more research is necessary to determine efficacy and safety [77].


ADT is usually reserved for older men and for treatment of men with more advanced disease. The therapy is based on the premise that androgens can stimulate prostate cancer growth [10,16,92]. ADT can include either orchiectomies or medical castration with a GnRH agonist and has been shown to achieve significant responses in more than 80% of treated patients [93].

Most men are treated with a GnRH agonist rather than bilateral orchiectomies, as GnRH agonists are easily administered, reversible, and more acceptable to patients. GnRH agonist use has risen markedly over the last 2 decades across all ages, disease stages, and tumor grades [94]. More than one-third of the estimated 2 million prostate cancer survivors in the United States are treated with GnRH agonists [10]. GnRH agonists have been shown to improve disease-free and overall survival in combination with radiation for locally advanced or high-risk nonmetastatic disease [95]. Adjuvant therapy with a GnRH agonist also improves survival in men with node-positive disease after radical prostatectomy [96].

ADT is also used in situations in which there are less clear benefits. PSA monitoring after primary therapy often detects recurrences long before they are revealed by either symptoms or imaging [97]. A rising PSA after primary surgery or radiation therapy commonly leads to long-term ADT, although the effects of early ADT on elevated PSA recurrences have not been adequately characterized. Additionally, some men with localized disease opt for long-term ADT instead of radiation or surgery, which has not been shown to improve survival rates relative to observation [98].

It is important to note that ADT, and especially the use of GnRH agonists, leads to a significant reduction in serum testosterone and a number of physiologic changes in bone mineral density, body composition, lipid profiles, and insulin sensitivity [14]. Men receiving GnRH agonists are at an increased risk for bone fracture as well as diabetes and cardiovascular disease [14,99]. The increased risk of diabetes and cardiovascular disease may explain in part the excess number of noncancer deaths associated with ADT. GnRH agonists significantly increase fat mass and fasting insulin levels and decrease insulin sensitivity [100,101]. Treatment-related changes in serum lipoproteins and arterial stiffness, as well as possible QT interval prolongation, may also contribute to the association between GnRH agonists and adverse cardiovascular effects [14,102]. Although ADT has improved outcomes in metastatic prostatic cancer patients, research is needed to address the adverse effects often seen with this therapy.


Cytotoxic chemotherapy has shown promise in treating prostate cancer after periods when previous treatment has fallen short. Results of the TAX 327 clinical trial indicated that treatment with docetaxel and prednisone (given every three weeks) led to superior survival and improved response in patients' pain, PSA levels, and quality of life [73]. Meanwhile, the SWOG 99-16 clinical trial noted an increase in median survival rate with docetaxel and estramustine treatment; however, greater toxicity is noted with this treatment [74]. These clinical trials established docetaxel as the standard chemotherapeutic treatment for prostate cancer. Other chemotherapy options are also being explored to improve patient outcomes. The combinations of mitoxantrone-prednisone and cabazitaxel-prednisone are often used to treat prostate cancer.

Other therapies are being developed for patients who are docetaxel-resistant. Many of the newer chemotherapies have monoclonal antibodies for targeting angiogenesis. This treatment strategy relies on suppressing several angiogenic proteins, including those in the VEGF family and endothelin (ET)-A, that are expressed in prostatic tissue and may cause prostate cancer [103,104,105]. Preliminary research using a combination of the monoclonal antibody bevacizumab, which acts against VEGF-A, and docetaxel have shown some positive results in patients experiencing docetaxel failure [106]. The Cancer and Leukemia Group B (CALGB) phase III trial in the United States (CALGB 90401) was conducted to determine if adding the monoclonal antibody bevacizumab to docetaxel and prednisone would increase overall survival rates [105]. Despite an improvement in progression-free survival and objective response, the addition of bevacizumab to docetaxel and prednisone did not improve overall survival in men with metastatic castration-resistant prostate cancer and was associated with greater toxicity [171].

Another novel angiogenic treatment pathway is the endothelin axis. Endothelin is a potent vasoconstrictor protein produced by the vascular endothelium. It has an important role in both vascular homeostasis and mediation of osteoblast growth and function [107]. In the normal prostate gland, endothelin-1 (ET-1) is produced by the prostate epithelial cells; its clearance is regulated through binding with the ET-B receptor (ETBR) and neural endopeptidase, which is responsible for the metabolism of several bioactive peptides [108]. In prostate cancer, ET-1 overexpression causes dysregulation of ET-1 components, specifically reducing ETBR binding and neural endopeptidase activity. Increased ET-1/ET-A receptor expression is observed during advanced prostate cancer. This dysregulated pathway is relevant in the link to bone metastases, because osteoblasts express ETAR in high density. Tumor-derived ET-1 promotes osteoblast proliferation and new bone formation through that receptor [109,110]. Thus, osteoblast proliferation generates other growth factors that appear to promote local metastatic bone formation [105]. Therapies that can effectively treat the spread of bone metastases are being investigated as future prostate cancer treatments.

Investigations continue into therapies such as atrasentan, which blocks the ET-1/ET-A receptor pathway and may therefore block the osteoblast role in promoting bone metastases in prostate cancer. Unfortunately, a randomized, phase III clinical trial comparing daily oral atrasentan with placebo in chemotherapy-naïve patients with recurrent prostate cancer despite chemical castration was unable to demonstrate a significant difference in the time to disease progression [111]. Nevertheless, patients receiving atrasentan showed smaller increases in levels of bone alkaline phosphatase (a marker for bone formation) than those in the placebo group [111]. Atrasentan with or without docetaxel was evaluated in a SWOG randomized study (SWOG S0421) focused on men with recurrent prostate cancer, with the goal of prolonging progression-free survival [105]. Atrasentan, when added to docetaxel, did not improve overall survival or progression-free survival in men with castration-resistant prostate cancer and bone metastases [165]. Meanwhile, other studies are focusing on docetaxel combinations with other antiangiogenic agents and monoclonal antibodies in recurrent disease patients. These include both early efficacy trials with thalidomide and exploratory trials with sorafenib, a potent multityrosine kinase inhibitor that blocks encoding by the genes BRAF, RAF1, KIT, KDR, and PDGFRB [105,112].


As noted previously, androgens influence the development of prostate cancer. Thus, decreasing androgen levels has been and remains a goal of prostate cancer treatment. This process has been discussed as part of ADT and the development of new pharmacotherapy approaches. The development of finasteride, an inhibitor of 5AR, the enzyme that converts testosterone to the more potent androgen dihydrotestosterone, has shown that lowering androgen levels in the prostate may reduce the risk of prostate cancer [113].

Three isoforms of 5AR have been identified; a separate gene encodes each isoform [114,115]. The type 1 isoform is prevalent in extraprostatic tissue (i.e., nongenital skin, the liver, and certain brain regions) and is present throughout life [4]. Several studies have suggested that type 1 5AR is also present in the prostate and foreskin [116]. Its expression is low in BPH tissue but increases steadily in prostatic intraepithelial neoplasia as well as in primary, recurrent, and metastatic prostate cancer. The type 2 isoenzyme of 5AR is prevalent in the prostate and is also present in the seminal vesicles, epididymis, and fetal genital skin [116]. More recently, another 5AR isoenzyme, type 3, has been discovered in hormone-refractory prostate cancer cells with little or no expression in normal adults. This isoenzyme appears to play a role in hormone-refractory prostate cancer growth and progression, but its potential role in prostate cancer remains under investigation [115].

The activity of 5AR is different in various ethnic groups, and it has been found to be greater among groups with increased incidences of prostate cancer [117]. Studies indirectly estimating 5AR activity have shown elevated activity among white men compared with Chinese American men and with white and African American men compared to Japanese American men [118]. Wu and colleagues documented this development by calculating DHT-to-testosterone ratios to indirectly measure the activity of 5AR [119]. The ratio was significantly lower among Chinese Americans than among whites and African Americans, but the difference between African Americans and whites was not statistically significant. The DHT-to-testosterone ratio was found to be lower (but not significant) among Asian-born Asians than among North American-born Asians; this is notable as greater incidences of prostate cancer have been observed among Japanese-born men who immigrate to the United States [59]. A study of a community-based sample of 1,899 men in Boston (age range: 30 to 79 years) reported significantly greater DHT-to-testosterone ratios in African American men compared to white and Hispanic men, suggesting African American men had greater 5AR activity [120].

Finasteride is a low-toxicity chemopreventive agent that inhibits the conversion of testosterone to the more potent androgen DHT within the prostate. It originally became available for the treatment of BPH, and since then, it has been approved for the treatment of male pattern baldness. However, little is known about its long-term effects on the prostate. Thompson and colleagues undertook a study to determine whether finasteride can reduce the prevalence of prostate cancer among initially healthy men during a seven-year period [113]. Data from the PCPT, one of only two completed randomized prostate cancer risk reduction trials (as of 2013), showed a 24.8% reduction in prostate cancer prevalence with the use of finasteride (18.4%) compared to the placebo group (24.4%). However, there was a greater incidence of high-grade cancers (Gleason scores: 7–10) found in the finasteride arm (37%) versus placebo (22.2%) [43]. This higher incidence of high-grade tumors was likely due to confounding factors than to an actual increase in aggressive cancers [43,113]. An 18-year follow-up study of the PCPT published in 2013 found that despite the increased incidence of high-grade cancers in the finasteride group compared to the placebo group, there was no significant between-group difference in the rates of overall survival or survival after the diagnosis of prostate cancer [41]. Men taking 5AR inhibitors for the management of BPH/lower urinary tract symptoms may also benefit from chemoprevention, and this added therapeutic benefit is promising for future investigation.

Given the initial findings of the PCPT, the American Society of Clinical Oncology and AUA Practice Guidelines Committee jointly convened a panel of experts to develop evidence-based recommendations on the role of 5AR inhibitors in the treatment of prostate cancer [121]. The dose of finasteride used to treat male pattern baldness is 1 mg per day; the PCPT utilized a dose of 5 mg per day. It is unknown if a 1 mg dose is as effective as 5 mg in reducing the risk of prostate cancer. If the lower dose is as effective, the balance of benefits and harms would be more favorable. All of this information is critical to making more reliable estimates of cost effectiveness of 5AR inhibitors for preventing prostate cancer [121]. It should be noted that 5AR inhibitors reduce but do not fully eliminate the risk of developing prostate cancer.

The Reduction by Dutasteride of Prostate Cancer Events (REDUCE) trial was a 4-year, multicenter, randomized, double-blind, and placebo-controlled study evaluating the efficacy and safety of oral dutasteride (0.5 mg/day) in reducing the incidence of prostate cancer among men identified as being at increased risk for the disease (PSA between 2.5 and 10 ng/mL) [122]. Dutasteride differs from finasteride in that it inhibits both 5AR isoenzymes 1 and 2. The REDUCE trial also attempted to find the reason for an increased incidence of 5AR inhibitor-associated high-grade prostate cancer tumors [43]. Data from the REDUCE trials show a significant decrease in prostate cancer incidence in dutasteride-treated patients during the 4 years (relative risk reduction: 23%), affirming the continuing investigation of 5AR inhibitors as a preventative treatment of prostate cancer [72]. In the dutasteride group, cancer was detected in 659 of the 3,305 men, compared with 858 of the 3,424 men in the placebo group. Whether dutasteride increases the incidence of high-grade tumors was unclear. In the dutasteride group, 29 men had tumors with a Gleason score of 8 to 10, compared with 19 in the placebo group. However, 141 men with tumors with a Gleason score of 5 to 7 were removed from the study during the first 2 years. It is speculated that the difference in number of high-grade tumors between groups would be statistically insignificant had these men not dropped out [146].


Primary care physicians, nurses, and other healthcare professionals who see patients on a regular basis play an important role in the follow-up evaluation for men who opt for watchful waiting/active surveillance, as well as for those who have been treated by an oncologist. After treatment for prostate cancer, men should be followed up with a history and physical examination and PSA testing every 6 months for 5 years and annually thereafter; they should also receive a DRE annually [125]. Primary care clinicians can also aid in the management of the side effects of treatment.



One key consideration for prostate cancer patients is the potential sexual side effects related to the available treatment options. Radical prostatectomy, radiation therapy, cryotherapy, and hormone therapy are all associated with a potential for decreased libido and erectile dysfunction. In one study of 2,636 men being treated for prostate cancer, 85% indicated they experienced problems with sexual potency; approximately one-third disclosed having sexual dysfunction prior to treatment [130]. In fact, this potential complication of cancer treatment, which can have devastating effects on quality of life and satisfaction with the care received, may result in men delaying or avoiding treatment altogether.

In the past, erectile dysfunction was often a silent condition, with many men being too embarrassed or ashamed to discuss the issue with their physicians. Today, there are many treatment options available to manage erectile dysfunction, including oral drug therapy, injection medications, suppositories or pellets that are deposited in the urethra of the penis, and surgery to insert penile implants or prostheses [126]. The most common approach is oral medication therapy with a phosphodiesterase-5 inhibitor (sildenafil, vardenafil, or tadalafil); it is unclear how many post-treatment patients will benefit from the use of these medications [126]. In one study, only 38% of patients who had received either definitive radiotherapy or prostatectomy for localized prostate cancer reported improvements in sexual functions as the result of medication interventions [131].

The FDA has issued mandates to revise labeling of phosphodiesterase-5 inhibitors. In 2005, the agency required the labels for all three of the agents to reflect the possibility of sudden vision loss after taking the drugs for a period of time [127]. The alert was associated with several case reports that suggested a temporal association between use of one of the drugs and nonarteritic anterior ischemic optical neuropathy (NAION), a cause of irreversible vision loss [127]. However, subsequent studies showed that the risk of NAION was similar among men who were and were not taking a phosphodiesterase-5 inhibitor; the risk of "possible" NAION was increased [128,129]. Still, some researchers have suggested that an examination of the fundus be performed on men who may be at higher risk for NAION before a phosphodiesterase-5 inhibitor is prescribed [127]. Patients should be properly educated regarding the potential effects of both prostate cancer treatments and medications available to manage post-treatment sexual dysfunction.


A diagnosis of prostate cancer is often the cause of psychological distress, and some men may become depressed as a result of the effect of the cancer or treatment. As discussed, the treatments available for prostate cancer patients can have significant effects on men's quality of life, negatively impacting self-esteem, relationships, and personal identity. Unfortunately, depression is underdiagnosed in men as the result of a divergence of factors, including clinicians' lack of appropriate training and discomfort with dealing with depression and issues related to male gender identity, such as:

  • Reluctance of men to seek help

  • Lack of men's recognition of the symptoms of depression

  • Hesitancy of men to express emotions

  • Inconsistency of men's symptoms with those in the Diagnostic and Statistical Manual of Mental Disorders

  • Tendency for men to see depression as a weakness

  • Men's misconceptions about mental illness and its treatment

Depression that is associated with chronic illness is often seen as an inevitable consequence of the disease, but the depression should be treated. Frequently, the treatment improves the overall outcome and can elevate quality of life [132]. The treatment approach will depend on the severity of symptoms and the patient's preference. In general, a combination of psychotherapy and pharmacologic management provides the best results for most men [132,133]. Potential psychotherapy approaches include cognitive behavior therapy and interpersonal psychotherapy [133,134,135].


Language and cultural barriers have the potential for far-reaching effect, given the growing percentages of racial/ethnic populations. As noted, patient understanding of the risks and benefits of treatment options is an essential aspect of prostate cancer care, and it must be assured that all patients have a clear understanding of the concepts discussed. When there is an obvious disconnect in the communication process between the practitioner and patient due to the patient's lack of proficiency in the English language, an interpreter is required.

According to U.S. Census Bureau data from 2011, 21% of the American population speak a language other than English, and of those, 42% speak English less than "very well" [136]. Clinicians should ask their patients what language they prefer for their medical care information, as some individuals prefer their native language even though they have said they can understand and discuss symptoms in English [137]. Translation services should be provided for patients who do not understand the clinician's language. "Ad hoc" interpreters (family members, friends, bilingual staff members,) are often used instead of professional interpreters for a variety of reasons, including convenience and cost. However, clinicians should check with their state's health officials about the use of ad hoc interpreters, as several states have laws about who can interpret medical information for a patient [138]. Even when allowed by law, the use of a patient's family member or friend as an interpreter should be avoided, as the patient may not be as forthcoming with information and the family member or friend may not remain objective [138]. Children should especially be avoided as interpreters, as their understanding of medical language is limited and they may filter information to protect their parents or other adult family members [138]. Individuals with limited English language skills have actually indicated a preference for professional interpreters rather than family members [139].

Most important, perhaps, is the fact that clinical consequences are more likely with ad hoc interpreters than with professional interpreters [140]. A systematic review of the literature showed that the use of professional interpreters facilitates a broader understanding and leads to better clinical care than the use of ad hoc interpreters, and many studies have demonstrated that the lack of an interpreter for patients with limited English proficiency compromises the quality of care and that the use of professional interpreters improves communication (errors and comprehension), utilization, clinical outcomes, and patient satisfaction with care [141,142].

Clinicians should use plain language in their discussions with their patients who have low literacy or limited English proficiency. They should ask them to repeat pertinent information in their own words to confirm understanding, and reinforcement with the use of low-literacy or translated educational materials may be helpful.


Patient A is an active man, 59 years of age, who missed his last yearly DRE and PSA. The results of these tests had been within normal limits in all previously elected examinations. At his next examination, a firm prostate nodule, approximately 2 mm in diameter, is palpated, and the PSA level is 14 ng/mL. A needle biopsy of the prostate is performed within 1 week of the PSA measurement. The biopsy shows several sites containing cells indicative of adenocarcinoma of the prostate, with a Gleason score of between 8 and 9.

After carefully evaluating the treatment options for an aggressive tumor, Patient A chooses radical prostatectomy and seeks care at an institution where nerve-sparing surgery is performed with the assistance of a robotic, computer-controlled device, to help reduce the risk of adverse events. According to the pathology report, the tumor is an adenocarcinoma that has extended beyond the capsule of the gland but has not involved the seminal vesicles.

Staging studies, including magnetic resonance imaging of the pelvis and abdomen and a bone scan, confirm the extent of the tumor and demonstrate lack of lymph node involvement or distant metastasis (T3a, N0, M0). Because of the T3a finding, a course of external radiation therapy to the local site is prescribed.

At the 3-month follow-up visit, the PSA level has increased to 20 ng/mL, and a bone scan demonstrates multiple skeletal lesions, primarily in the ribs, pelvis, and skull, none of which had been seen on the previous scan. Due to the rapid progression of disease and the metastatic lesions, the patient's survival is estimated to be less than 3 years.

After a discussion with his surgeon, oncologist, and urologist, the patient decides to forego ADT, choosing instead treatment consisting of chemotherapy with docetaxel in combination with the angiogenesis inhibitor bevacizumab over a course of several months. The treatment causes some nausea, malaise, and hair loss, but the patient tolerates the effects well. His primary complaint is of oral ulcers, which require topical treatment. The PSA level drops steadily during follow-up, reaching a level of 0.4 ng/mL after approximately 6 months of treatment.

Patient A continues to feel well after 2 years of follow-up, and the PSA level has remained at 0.2 ng/mL or less. Incontinence that was present after the surgery has ended, but erectile dysfunction remains, despite the use of medications.


Prostate cancer is a potentially debilitating illness that affects work, interpersonal relationships, and overall quality of life. Evidence has shown that if caught early, this cancer can be treated effectively. However, there are disagreements related to the risks and benefits of screening, which may interfere with early diagnosis. Healthcare professionals must be familiar with key concepts related to the diagnosis and screening of prostate cancer in order to best treat these patients. They must also be familiar with emerging trends, such as diet, that can be effective for prostate cancer and other diseases as well.

Standard prostate cancer therapies, such as surgery, radiation, chemotherapy, and ADT, can relieve symptoms in some patients and provide partial improvement in others. However, some patients may have prostate cancer that is refractory to treatment, and knowledge of more experimental therapies can be helpful to patient outcomes. Effectively treating prostate cancer, whether by standard therapy or emerging treatments, can be beneficial to both healthcare professionals and their patients.


Prostate Cancer Foundation (PCF)
An organization that investigates new treatments and an eventual cure for prostate cancer. The PCF has funded more than 1,500 programs at nearly 200 research centers in 20 countries around the world.
Zero: The End of Prostate Cancer
An organization that provides comprehensive patient treatment information, educates high-risk populations, and conducts free prostate cancer testing throughout the United States. It obtains research funds from the federal government to find new treatments and to pursue a better test for the disease.
Patient Advocates for Advanced (Prostate) Cancer Treatments (PAACT), Inc.
An organization that helps to identify new developments and treatment options for patients who have prostate cancer.
American Cancer Society
A nationwide, community-based, voluntary health organization dedicated to preventing cancer, saving lives, and diminishing suffering from cancer through research, education, advocacy, and service.

Works Cited

1. Siegel R, Naishadham D, Jemal A. Cancer statistics, 2013. CA Cancer J Clin. 2013;63(1):11-30.

2. American Cancer Society. American Cancer Society guideline for the early detection of prostate cancer: update 2010.CA Cancer J Clin. 2010;60(2):70-98.

3. Horner M, Ries L, Krapcho M, et al. (eds). SEER Cancer Statistics Review, 1975–2006. Bethesda, MD: National Cancer Institute; 2009.

4. Crawford ED. Understanding the epidemiology, natural history, and key pathways involved in prostate cancer. Urology. 2009;73(Suppl 5):S4-S10.

5. Bostwick DG, Burke HB, Djakiew D, et al. Human prostate cancer risk factors. Cancer. 2004;101(10 Suppl):2371-2490.

6. Platz EA, Rimm EB, Willett WC, Kantoff PW, Giovannucci E. Racial variation in prostate cancer incidence and in hormonal system markers among male health professionals. J Nat Cancer Inst. 2000;92(24):2009-2017.

7. Yin M, Bastacky S. Chandran U, Becich MJ, Dhir R. Prevalence of incidental prostate cancer in the general population: a study of healthy organ donors. J Urol. 2008;179(3):892-895.

8. Platz EA, Giovannucci E. The epidemiology of sex steroid hormones and their signaling and metabolic pathways in the etiology of prostate cancer. J Steroid Biochem Mol Biol. 2004;92(4):237-253.

9. Brown BW, Brauner C, Minnotte MC. Noncancer deaths in white adult cancer patients. J Natl Cancer Inst. 1993;85(12):979-987.

10. Keating NL, O'Malley AJ, Smith MR. Diabetes and cardiovascular disease during androgen deprivation therapy for prostate cancer. J Clin Oncol. 2006;24(27):4448-4456.

11. Scardino PT. The Gordon Wilson lecture: natural history and treatment of early-stage prostate cancer. Trans Am Clin Climatol Assoc. 2000;111:201-241.

12. Miller GJ, Torkko KC. Natural history of prostate cancer: epidemiologic considerations. Epidemiol Rev. 2001;23(1):14-18.

13. Theodorescu D. Prostate cancer, clinical oncology. In: Schwab M (ed). Encyclopedic Reference of Cancer. 1st ed. New York, NY: Springer; 2001.

14. McNeal JE. The zonal anatomy of the prostate. Prostate. 1981;2(1):35-49.

15. Miller GJ, Cygan JM. Morphology of prostate cancer: the effects of multifocality on histological grade, tumor volume and capsule penetration. J Urol. 1994;152(5 pt 2):1709-1713.

16. Huggins C, Hodges CV. Studies on prostate cancer: I. The effect of castration, of estrogen and of androgen injection on serum phosphatases in metastatic carcinoma of the prostate. J Urol. 2002;168(1):9-12.

17. Wilbert DM, Griffin JE, Wilson JD. Characterization of the cytosol androgen receptor of the human prostate. J Clin Endocrinol Metab. 1983;56(1):113-120.

18. Marks LS. 5alpha-reductase: history and clinical importance. Rev Urol. 2004;6(suppl 9):S11-S21.

19. Zhu YS, Sun GH. 5α-reductase isoenzymes in the prostate. J Med Sci. 2005;25(1):1-12.

20. Catalona WJ, Smith DS, Ratliff TL, et al. Measurement of prostate-specific antigen in serum as a screening test for prostate cancer. N Eng J Med. 1991;324(17):1156-1161.

21. Okotie OT, Roehl KA, Han M, Loeb S, Gashti SN, Catalona WJ. Characteristics of prostate cancer detected by digital rectal examination only. Urology. 2007;70(6):1117-1120.

22. Loeb S, Schaeffer EM. Risk factors, prevention and early detection of prostate cancer. Prim Care. 2009;36(3):603-621.

23. Schwartz K, Deschere B, Xu J. Screening for prostate cancer: who and how often? J Fam Pract. 2005;54(7):586-596.

24. Nadler RB, Humphrey PA, Smith DS, Catalona WJ, Ratliff TL. Effect of the inflammation and benign prostatic hyperplasia on elevated serum prostate specific antigen levels. J Urol. 1995;154(2 Pt 1):407-413.

25. Nelson WG, DeWeese TL, DeMarzo AM. The diet, prostate inflammation, and the development of prostate cancer. Cancer Metastasis Rev. 2002;21(1):3-16.

26. Penson DF, Rossignol M, Sartor AO, Scardino PT, Abenhaim LL. Prostate cancer: epidemiology and health-related quality of life. Urology. 2008;72(Suppl 6):S3-S11.

27. Krumholtz JS, Carvalhal GF, Ramos CG, et al. Prostate-specific antigen cutoff of 2.6 ng/ml for prostate cancer screening is associated with favorable tumor features. Urology. 2002;60(3):469-474.

28. Gleason DF. Histologic grading and clinical staging of prostatic carcinoma. In: Tannenbaum M (ed). Urology Pathology: The Prostate. Philadelphia, PA: Lea & Febiger; 1977.

29. Carter HB, Allaf ME, Partin AW. Diagnosis and staging of prostate cancer. In: Wein A, Kovoussi L, Novick A, Partin A, Peters C (eds). Campbell-Walsh Urology. 9th ed. Philadelphia, PA: Saunders Elsevier; 2007: 2927.

30. D'Amico AV, Whittington R, Malkowicz SB, et al. Biochemical outcome after radical prostatectomy, external beam radiation therapy, or interstitial radiation therapy for clinically localized prostate cancer. JAMA. 1998;280(11):969-974.

31. Dall'Era MA, Kane CJ. Watchful waiting versus active surveillance: appropriate patient selection. Curr Urol Rep. 2008;9(3): 211-216.

32. McNaughton Collins M, Ransohoff DF, Barry MJ. Early detection of prostate cancer: serendipity strikes again. JAMA. 1997;278(18):1516-1519.

33. Etzioni R, Berry KM, Legler JM, Shaw P. Prostate-specific antigen testing in black and white men: an analysis of medicare claims from 1991 to 1998. Urology. 2002;59(2):251-255.

34. National Comprehensive Cancer Network. NCCN Practice Guidelines in Oncology: Prostate Cancer Early Detection. Version 2.2012. Available at http://www.nccn.org. Last accessed October 1, 2013.

35. Lim LS, Sherin K, ACPM Prevention Practice Committee. Screening for prostate cancer in U.S. men: ACPM position statement on preventive practice. Am J Prev Med. 2008;34(2):164-170.

36. U.S. Preventive Services Task Force. Screening for Prostate Cancer: Current Recommendation. Available at http://www.uspreventiveservicestaskforce.org/prostatecancerscreening.htm. Last accessed September 30, 2013.

37. Qaseem A, Barry MJ, Denberg TD, et al. Screening for prostate cancer: a guidance statement from the Clinical Guidelines Committee of the American College of Physicians. Ann Intern Med. 2013;158(10):761-769.

38. Wolf AM, Wender RC, Etzioni RB, et al. American Cancer Society guideline for the early detection of prostate cancer: update 2010. CA Cancer J Clin. 2010;60(2):70-98.

39. Carter HB, Albertsen PC, Barry MJ, et al. Early Detection of Prostate Cancer: AUA Guideline. Available at http://www.auanet.org/common/pdf/education/clinical-guidance/Prostate-Cancer-Detection.pdf. Last accessed September 30, 2013.

40. Pienta KJ. Critical appraisal of prostate-specific antigen in prostate cancer screening: 20 years later. Urology. 2009;73(Suppl 5): S11-S20.

41. Thompson IM Jr, Goodman PJ, Tangen CM, et al. Long-term survival of participants in the prostate cancer prevention trial.N Engl J Med. 2013;369(7):603-610.

42. Tarone RE, Chu KC, Brawley OW. Implications of stage-specific survival rates in assessing recent declines in prostate cancer mortality rates. Epidemiology. 2000;11(2):167-170.

43. Bouchardy C, Fioretta G, Rapiti E, et al. Recent trends in prostate cancer mortality show a continuous decrease in several countries. Int J Cancer. 2008;123(2):421-429.

44. Thompson IM, Pauler DK, Goodman PJ, et al. Prevalence of prostate cancer among men with a prostate-specific antigen level ≤ or = 4.0 ng per milliliter. N Engl J Med. 2004;350(22):2239-2246.

45. Hodge KK, McNeal JE, Terris MK, Stamey TA. Random systematic versus directed ultrasound guided transrectal core biopsies of the prostate. J Urol. 1989;142(1):71-75.

46. Norberg M, Egevad L, Holmberg L, Sparén P, Norlén BJ, Busch C. The sextant protocol for ultrasound-guided core biopsies of the prostate underestimates the presence of cancer. Urology. 1997;50(4):562-566.

47. Emiliozzi P, Scarpone P, DePaula F, et al. The incidence of prostate cancer in men with prostate specific antigen greater than 4.0 ng/ml: a randomized study of 6 versus 12 core transperineal prostate biopsy. J Urol. 2004;171(1):197-199.

48. Stewart CS, Leibovich BC, Weaver AL, Lieber MM. Prostate cancer diagnosis using a saturation needle biopsy technique after previous negative sextant biopsies. J Urol. 2001;166(1):86-91.

49. Andriole GL, Crawford ED, Grubb RL III, et al. Prostate cancer screening in the randomized Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial: mortality results after 13 years of follow-up. J Natl Cancer Inst. 2012;104(2):125-132.

50. Schröder FH, Hugosson J, Roobol MJ, et al. Screening and prostate-cancer mortality in a randomized European study. N Engl J Med. 2009;360(13):1320-1328.

51. Parekh DJ, Ankerst DP, Higgins BA, et al. External validation of the Prostate Cancer Prevention Trial risk calculator in a screened population. Urology. 2006;68:1152-1155.

52. Nam RK, Toi A, Klotz LH, et al. Assessing individual risk for prostate cancer. J Clin Oncol. 2007;25(24):3582-3588.

53. Katz MS, Efstathiou JA, Nquyen PL, Zietman AL. CaP Calculator: an online decision support tool to improve evidence-based doctor-patient communication for clinically localized prostate cancer. Int J Radiat Oncol Biol Phys. 2008;72(Suppl 1):S41.

54. Chan JM, Gann PH, Giovannucci EL. Role of diet in prostate cancer development and progression. J Clin Oncol. 2005;23(32):8152-8160.

55. Hedelin M, Bälter KA, Chang ET, et al. Dietary intake of phytoestrogens, estrogen receptor-beta polymorphisms and the risk of prostate cancer. Prostate. 2006;66(14):1512-1520.

56. Joseph MA, Moysich KB, Freudenheim JL, et al. Cruciferous vegetables, genetic polymorphisms in glutathione S-transferases M1 and T1, and prostate cancer risk. Nutrition Cancer. 2004;50(2):206-213.

57. Carmody J, Olendzki B, Reed G, Andersen V, Rosenzweig P. A dietary intervention for recurrent prostate cancer after definitive primary treatment: results of a randomized pilot trial. Urology. 2008;72(6):1324-1328.

58. Blanchard C, Stein K, Baker F, et al. Association between current lifestyle behaviors and health-related quality of life in breast, colorectal, and prostate cancer survivors. Psychol Health. 2004;19(1):1-13.

59. Dunn JE. Cancer epidemiology in populations of the United States—with emphasis on Hawaii and California—and Japan.Cancer Res. 1975;35(11 Pt 2):3240-3245.

60. Rodriguez C, McCullough ML, Mondul AM, et al. Meat consumption among black and white men and risk of prostate cancer in the Cancer Prevention Study II Nutrition Cohort. Cancer Epidemiol Biomarkers Prev. 2006;15(2):211-216.

61. Park SY, Murphy SP, Wilkens LR, Henderson BE, Kolonel LN. Fat and meat intake and prostate cancer risk: the multiethnic cohort study. Int J Cancer. 2007;121(6):1339-1345.

62. Klein EA, Thompson IM, Lippman SM, et al. SELECT: the next prostate cancer prevention trial. J Urology. 2001;66(4):1311-1315.

63. Klein EA, Thompson IM Jr, Tangen CM, et al. Vitamin E and the risk of prostate cancer: the Selenium and Vitamin E Cancer Prevention Trial (SELECT). JAMA. 2011;306(14):1549-1556.

64. Gao X, LaValley MP, Tucker KL. Prospective studies of dairy product and calcium intakes and prostate cancer risk: a meta-analysis. J Natl Cancer Inst. 2005;97(23):1768-1777.

65. Yan L, Spitznagel EL. Meta-analysis of soy food and risk of prostate cancer in men. Int J Cancer. 2005;117(4):667-669.

66. Giovannucci E, Rimm EB, Liu Y, Stampfer MJ, Willett WC. A prospective study of tomato products, lycopene, and prostate cancer risk. J Natl Cancer Inst. 2002;94(5):391-398.

67. Kavanaugh CJ, Trumbo PR, Ellwood KC. The U.S. Food and Drug Administration's evidence-based review for qualified health claims: tomatoes, lycopene, and cancer. J Natl Cancer Inst. 2007;99(14):1074-1085.

68. Moyad MA. Fat reduction to prevent prostate cancer: waiting for more evidence? Curr Opin Urol. 2001;11(5):457-461.

69. Krishnan AV, Feldman D. Molecular pathways mediating the anti-inflammatory effects of calcitriol: implications for prostate cancer chemoprevention and treatment. Endocr Relat Cancer. 2010;17(1):R19-R38.

70. Jacobs EJ, Rodriguez C, Mondul AM, et al. A large cohort study of aspirin and other nonsteroidal anti-inflammatory drugs and prostate cancer incidence. J Natl Cancer Inst. 2005;97(13):975-980.

71. Mahmud SM, Franco EL, Aprikian AG. Use of nonsteroidal anti-inflammatory drugs (NSAIDs) and prostate cancer risk: a meta-analysis. Int J Cancer. 2010;127(7):1680-1691.

72. Andriole GL, Bostwick DG, Brawley OW, et al. Effect of dutasteride on the risk of prostate cancer. N Engl J Med. 2010;362(13): 1192-1202.

73. Tannock IF, de Wit R, Berry WR, et al. Docetaxel plus prednisone or mitoxantrone plus prednisone for advanced prostate cancer.N Engl J Med. 2004;351(15):1502-1512.

74. Petrylak DP, Tangen CM, Hussain MH, et al. Docetaxel and estramustine compared with mitoxantrone and prednisone for advanced refractory prostate cancer. N Engl J Med. 2004;351(15):1513-1520.

75. Bill-Axelson A, Holmberg L, Filén F, et al. Radical prostatectomy versus watchful waiting in localized prostate cancer: the Scandinavian prostate cancer group-4 randomized trial. J Natl Cancer Inst. 2008;100(16):1144-1154.

76. Gonzalgo ML, Patil N, Su LM, Patel VR. Minimally invasive surgical approaches and management of prostate cancer. Urol Clin N Am. 2008;35(3):489-504.

77. National Cancer Institute. Prostate Cancer Treatment: Treatment Option Overview. Available at http://www.cancer.gov/cancertopics/pdq/treatment/prostate/HelathProfessional/page4. Last accessed October 16, 2013.

78. Babaian R, Donnelly B, Bahn D, et al. Best Practice Policy Statement on Cryosurgery for the Treatment of Localized Prostate Cancer. Linthicum, MD: American Urological Association; 2008.

79. Cohen JK, Miller RJ Jr, Ahmed S, Lotz MJ, Baust J. Ten-year biochemical disease control for patients with prostate cancer treated with cryosurgery as primary therapy. Urology. 2008;71(3):515-518.

80. Macdonald OK, Lee RJ, Snow G, et al. Prostate-specific antigen control with low-dose adjuvant radiotherapy for high-risk prostate cancer. Urology. 2007;69(2):295-299.

81. Hanks GE, Pajak TF, Porter A, et al. Phase III trial of long-term adjuvant androgen deprivation after neoadjuvant hormonal cytoreduction and radiotherapy in locally advanced carcinoma of the prostate: the Radiation Therapy Oncology Group Protocol 92-02. J Clin Oncol. 2003;21(21):3972-3978.

82. Beyer DC, McKeough T, Thomas T. Impact of short course hormonal therapy on overall and cancer specific survival after permanent prostate brachytherapy. Int J Radiat Oncol Biol Phys. 2005;61(5):1299-1305.

83. Anscher MS, Robertson CN, Prosnitz R. Adjuvant radiotherapy for pathologic stage T3/4 adenocarcinoma of the prostate: ten-year update. Int J Radiat Oncol Biol Phys. 1995;33(1):37-43.

84. Valicenti RK, Gomella LG, Ismail M, Mullholland SG, Peterson RO, Corn BW. Pathologic seminal vesicle invasion after radical prostatectomy for patients with prostate carcinoma: effect of early adjuvant radiation therapy on biochemical control. Cancer. 1998;82(10):1909-1914.

85. Petrovich Z, Lieskovsky G, Langholz B, Jozsef G, Streeter OE Jr, Skinner DG. Postoperative radiotherapy in 423 patients with pT3N0 prostate cancer. Int J Radiat Oncol Biol Phys. 2002;53(3):600-609.

86. Leibovich BC, Engen DE, Patterson DE, et al. Benefit of adjuvant radiation therapy for localized prostate cancer with a positive surgical margin. J Urol. 2000;163:1178-1182.

87. Eisbruch A, Perez CA, Roessler EH, Lockett MA. Adjuvant irradiation after prostatectomy for carcinoma of the prostate with positive surgical margins. Cancer. 1994;73(2):384-388.

88. Meier R, Mark R, St Royal L, Tran L, Colburn G, Parker R. Postoperative radiation therapy after radical prostatectomy for prostate carcinoma. Cancer. 1992;70(7):1960-1966.

89. Thompson IM Jr, Tangen CM, Paradelo J, et al. Adjuvant radiotherapy for pathologically advanced prostate cancer: a randomized clinical trial. JAMA. 2006;296(19):2329-2335.

90. Bolla M, van Poppel H, Collette L, et al. Postoperative radiotherapy after radical prostatectomy: a randomized controlled trial (EORTC trial 22911). Lancet. 2005;366(9485):572-578.

91. Wiegel T, Bottke D, Willich N, et al. Phase III results of adjuvant radiotherapy (RT) versus "wait and see" (WS) in patients with pT3 prostate cancer following radical prostatectomy (RP) (ARO 96-02/AUO AP 09/95). J Clin Oncol. 2005;23(16S):4513.

92. Saylor PJ, Keating NL, Smith MR. Prostate cancer survivorship: prevention and treatment of the adverse effects of androgen deprivation therapy. J Gen Intern Med. 2009;24(Suppl 2):S389-S394.

93. Vogelzang NJ, Chodak GW, Soloway MS, et al. Goserelin versus orchiectomy in the treatment of advanced prostate cancer: final results of a randomized trial. Zoladex Prostate Study Group. Urology. 1995;46(2):220-226.

94. Barry MJ, Delorenzo MA, Walker-Corkery ES, Lucas Fl, Wennberg DC. The rising prevalence of androgen deprivation among older American men since the advent of prostate-sepcific antigen testing: a population-based cohort study. BJU Int. 2006;98(5):973-978.

95. D'Amico AV, Manola J, Loffredo M, Renshaw AA, DellaCroce A, Kantoff PW. 6-month androgen suppression plus radiation therapy vs. radiation therapy alone for patients with clinically localized prostate cancer: a randomized controlled trial. JAMA. 2004;292(7):821-827.

96. Messing EM, Manola J, Yao J, et al. Immediate versus deferred androgen deprivation treatment in patients with node-positive prostate cancer after radical prostatectomy and pelvic lymphadenectomy. Lancet Oncol. 2006;7(6):472-479.

97. Loblaw DA, Virgo KS, Nam R, et al. Initial hormonal management of androgen-sensitive metastatic, recurrent, or progressive prostate cancer: 2006 update of an American Society of Clinical Oncology practice guideline. J Clin Oncol. 2007;25(12): 1596-1605.

98. Lu-Yao GL, Albertsen PC, Moore DF, et al. Survival following primary androgen deprivation therapy among men with localized prostate cancer. JAMA. 2008;300(2):173-181.

99. Shahinian VB, Kuo YF, Freeman JL, Goodwin JS. Risk of fracture after androgen deprivation for prostate cancer. N Eng J Med. 2005;352(2):154-164.

100. Smith MR, Finkelstein JS, McGovern FJ, et al. Changes in body composition during androgen deprivation therapy for prostate cancer. J Clin Endocrinol Metab. 2002;87(2):599-603.

101. Smith MR, Lee H, Nathan DM. Insulin sensitivity during combined androgen blockade for prostate cancer. J Clin Endocrinol Metab. 2006;91(4):1305-1308.

102. Garnick MB, Pratt CM, Campion M, et al. The effect of hormonal therapy for prostate cancer on the electrocardiographic QT interval: phase III results following treatment with leuprolide and goserelin, alone or with bicalutamide and the GnRH antagonist abarelix. J Clin Oncol. 2004;22(14S):4578.

103. Kaushal V, Mukunyadzi P, Dennis RA, Siegel ER, Johnson DE, Kohli M. Stage-specific characterization of the vascular endothelial growth factor axis in prostate cancer: expression of lymphangiogenic markers is associated with advanced stage disease.Clin Cancer Res. 2005;11(2 Pt 1):584-593.

104. Guise TA, Mohammad KS. Endothelins in bone cancer metastases. Cancer Treat Res. 2004;118:197-212.

105. Kohli M, Tindall DJ. New developments in the medical management of prostate cancer. Mayo Clin Proc. 2010;85(1):77-86.

106. Di Lorenzo G, Figg WD, Fossa SD, et al. Combination of bevacizumab and docetaxel in docetaxel-pretreated hormone-refractory prostate cancer: a phase 2 study. Eur Urol. 2008;54(5):1089-1094.

107. Nelson J, Bagnato A, Battisini B, Nisen P. The endothelin axis: emerging role in cancer. Nat Rev Cancer. 2003;3(2):110-116.

108. Papandreou CN, Usmani B, Geng Y, et al. Neutral endopeptidase 24.11 loss in metastatic human prostate cancer contributes to androgen-independent progression. Nat Med. 1998;4(1):50-57.

109. Mundy GR. Endothelin-1 and osteoblastic metastasis. Proc Natl Acad Sci U S A. 2003;100(19):10588-10589.

110. Yin JJ, Mohammad KS, Käkönen SM, et al. A causal role for endothelin-1 in the pathogenesis of osteoblastic bone metastases.Proc Natl Acad Sci U S A. 2003;100(19):10954-10959.

111. Carducci MA, Saad F, Abrahamsson PA, et al. A phase 3 randomized controlled trial of the efficacy and safety of atrasentan in men with metastatic hormone-refractory prostate cancer. Cancer. 2007;110(9):1959-1966.

112. Dahut WL, Gulley JL, Arlen PM, et al. Randomized phase II trial of docetaxel plus thalidomide in androgen-independent prostate cancer. J Clin Oncol. 2004;22(13):2532-2539.

113. Thompson IM, Goodman PJ, Tangen CM, et al. The influence of finasteride on the development of prostate cancer. N Engl J Med. 2003;349(3):215-224.

114. Jenkins EP, Andersson S, Imperato-McGinley J, Wilson JD, Russell DW. Genetic and pharmacological evidence for more than one human steroid 5 alpha-reductase. J Clin Invest. 1992;89(1):293-300.

115. Uemura M, Tamura K, Chung S, et al. Novel 5 alpha-steroid reductase (SRD5A3, type-3) is overexpressed in hormone-refractory prostate cancer. Cancer Sci. 2008;99(1):81-86.

116. Thigpen AE, Silver RI, Guileyardo JM, Casey ML, McConnell JD, Russell DW. Tissue distribution and ontogeny of steroid 5 alpha-reductase isozyme expression. J Clin Invest. 1993;92(2):903-910.

117. Ross RK, Bernstein L, Lobo RA, et al. 5-alpha-reductase activity and risk of prostate cancer among Japanese and US white and black males. Lancet. 1992;339(8798):887-889.

118. Lookingbill DP, Demers LM, Wang C, Leung A, Rittmaster RS, Santen RJ. Clinical and biochemical parameters of androgen action in normal healthy Caucasian versus Chinese subjects. J Clin Endocrinol Metab. 1991;72(6):1242-1248.

119. Wu AH, Whittemore AS, Kolonel LN, et al. Serum androgens and sex hormone-binding globulins in relation to lifestyle factors in older African-American, white, and Asian men in the United States and Canada. Cancer Epidemiol Biomarkers Prev. 1995;4(7):735-741.

120. Litman HJ, Bhasin S, Link CL, Araujo AB, McKinlay JB. Serum androgen levels in black, Hispanic, and white men. J Clin Endocrinol Metab. 2006;91(11):4326-4334.

121. Kramer BS, Hagerty KL, Justman S, et al. Use of 5alpha-reductase inhibitors for prostate cancer chemoprevention: American Society of Clinical Oncology/American Urological Association 2008 Clinical Practice Guidelines. J Urol. 2009;181(4): 1642-1657.

122. ClinicalTrials.gov. REDUCE: A Clinical Research Study to Reduce the Incidence of Prostate Cancer in Men Who Are at Increased Risk. Available at http://clinicaltrials.gov/show/NCT00056407. Last accessed October 15, 2013.

123. Musquera M, Fleshner NE, Finelli A, Zlotta AR. The REDUCE trial: chemoprevention in prostate cancer using a dual 5alpha-reductase inhibitor, dutasteride. Expert Rev Anticancer Ther. 2008;8(7):1073-1079.

124. National Cancer Institute. Prostate Cancer Treatment: Stage Information. Available at http://www.cancer.gov/cancertopics/pdq/treatment/prostate/HealthProfessional/page4. Last accessed September 30, 2013.

125. Sunga AY, Eberi MM, Oeffinger KC, Hudson MM, Mahoney MC. Care of cancer survivors. Am Fam Phys. 2005;71(4):699-706.

126. Cleveland Clinic. Erectile Dysfunction Treatments for Patients with Prostate Cancer. Available at http://my.clevelandclinic.org/disorders/prostate_cancer/hic_erectile_dysfunction_treatments_for_patients_with_prostate_cancer.aspx. Last accessed October 16, 2013.

127. Pomeranz HD. Can erectile dysfunction drug use lead to ischaemic optic neuropathy? Br J Ophthalmol. 2006;90(2):127-128.

128. Tsertsvadze A, Yazdi F, Fink HA, et al. Oral phosphodiesterase-5 inhibitors and hormonal treatments for erectile dysfunction: a systematic review and meta-analysis. Ann Intern Med. 2009;151(9):650-661.

129. McGwin G Jr, Vaphiades MS, Hall TA, Owsley C. Non-arteritic anterior ischaemic optic neuropathy and the treatment of erectile dysfunction. Br J Ophthalmol. 2006;90(2):154-157.

130. Schover LR, Fouladi RT, Warneke CL, et al. Defining sexual outcomes after treatment for localized prostate carcinoma. Cancer. 2002;95(8):1773-1785.

131. Schover LR, Fouladi RT, Warneke CL, et al. The use of treatments for erectile dysfunction among survivors of prostate carcinoma. Cancer. 2002;95(11):2397-2407.

132. National Institute of Mental Health. Men and Depression. NIH Publication No. 05-4972. Bethesda, MD: National Institutes of Health; 2005.

133. Robbins A. Biopsychosocial aspects in understanding and treating depression in men: a clinical perspective. J Men's Health Gender. 2006;3(1):10-18.

134. Winkler D, Pjrek E, Kasper S. Anger attacks in depression-evidence for a male depressive syndrome. Psychother Psychosom. 2005;74(5):303-307.

135. Epperly TD, Moore KE. Health issues in men: part II. Common psychosocial disorders. Am Fam Phys. 2000;62(1):117-124.

136. U.S. Census U.S. Census Bureau. Language Spoken at Home: 2011 American Community Survey (ACS) 1-Year Estimates. Available at http://factfinder2.census.gov/faces/tableservices/jsf/pages/productview.xhtml?pid=ACS_11_1YR_S1601&prodType=table. Last accessed June 18, 2013.

137. Karliner L, Napoles-Springer AM, Schillinger D, Bibbins-Domingo K, Pérez-Stable EJ. Identification of limited English proficient patients in clinical care. J Gen Intern Med. 2008;23(10):1555-1560.

138. Sevilla Matir J, Willis DR. Using bilingual staff members as interpreters. Fam Pract Manage. 2004;11(7):34-36.

139. Ngo-Metzger Q, Massagli MP, Clarridge BR, et al. Linguistic and cultural barriers to care: perspectives of Chinese and Vietnamese immigrants. J Gen Intern Med. 2003;18(1):44-52.

140. Flores G. Language barriers to health care in the United States. N Engl J Med. 2006;355(3):229-231.

141. Flores G. The impact of medical interpreter services on the quality of health care: a systematic review. Med Care Res Rev. 2005;62(3):255-299.

142. Karliner L, Jacobs EA, Chen AH, Mutha S. Do professional interpreters improve clinical care for patients with limited English proficiency? A systematic review of the literature. Health Serv Res. 2007;42(2):727-754.

143. Blana A, Murat FJ, Walter B, et al. First analysis of the long-term results with transrectal HIFU in patients with localised prostate cancer. Eur Urol. 2008;53(6):1194-1201.

144. Berge V, Baco E, Dahl AA, Karlsen SJ. Health-related quality of life after salvage high-intensity focused ultrasound (HIFU) treatment for locally radiorecurrent prostate cancer. Int J Urol. 2011;18(9):646-651.

145. Challacombe BJ, Murphy DG, Zakri R, Cahill DJ. High-intensity focused ultrasound for localized prostate cancer: initial experience with a 2-year follow-up. BJU Int. 2009;104(2):200-204.

146. Klotz L. Words of wisdom. Re: Effect of dutasteride on the risk of prostate cancer. Andriole G, Bostwick D, Brawley O, et al.N Engl J Med. 2010;362:1192-202. Eur Urol. 2010;58(2):313.

147. Ratajczak C. Using the Free PSA Test to Help Estimate Prostate Cancer Risk Before Biopsy. Available at http://www.active-surveillance.com/christine/. Last accessed September 4, 2013.

148. National Guideline Clearinghouse. Screening for Prostate Cancer: Guideline Synthesis. Available at http://www.guideline.gov/syntheses/synthesis.aspx?id=46242. Last accessed October 1, 2013.

149. Basch E, Oliver TK, Vickers A, et al. Screening for prostate cancer with prostate-specific antigen testing: American Society of Clinical Oncology provisional clinical opinion. J Clin Oncol. 2012;30(24):3020-3025.

150. Moyer VA, U.S. Preventive Services Task Force. Screening for prostate cancer: recommendation statement. Ann Intern Med. 2012;157(2):120-134.

151. Mistry K, Cable G. Meta-analysis of prostate-specific antigen and digital rectal examination as screening tests for prostate carcinoma. J Am Board Fam Pract. 2003;16(2):95-101.

152. Ilic D, Neuberger MM, Djulbegovic M, Dahm P. Screening for prostate cancer. Cochrane Database Syst Rev. 2013;1:CD004720.

153. Draisma G, Boer R, Otto SJ, et al. Lead times and overdetection due to prostate-specific antigen screening: estimates from the European Randomized Study of Screening for Prostate Cancer. J Natl Cancer Inst. 2003;95:868-878.

154. Gulati R, Gore JL, Etzioni R. Comparative effectiveness of alternative prostate-specific antigen-based prostate cancer screening strategies: model estimates of potential benefits and harms. Ann Intern Med. 2013;158(3):143-153.

155. Stacey D, Bennett CL, Barry MJ, et al. Decision aids for people facing health treatment or screening decisions. Cochrane Database Syst Rev. 2011;(10):CD001431.

156. Ross LE, Powe BD, Taylor YJ, Howard DL. Physician-patient discussions with African American men about prostate cancer screening. Am J Mens Health. 2008;2(2):156-164.

157. McFall SL. U.S. men discussing prostate-specific antigen tests with a physician. Ann Fam Med. 2006;4(5):433-436.

158. Nam RK, Kattan MW, Chin JL, et al. Prospective multi-institutional study evaluating the performance of prostate cancer risk calculators. J Clin Oncol. 2011;29(22):2959-2964.

159. Vickers AJ. Prediction models: revolutionary in principle, but do they do more good than harm? J Clin Oncol. 2011;29(22):2951-2952.

160. Shariat SF, Karakiewicz PI, Roehrborn CG, Kattan MW. An updated catalog of prostate cancer predictive tools. Cancer. 2008;113(11):3075-3099.

161. Nam RK, Toi A, Klotz LH, et al. Assessing individual risk for prostate cancer. J Clin Oncol. 2007;25(24):3582-3588.

162. Thompson IM, Ankerst DP, Chi C, et al. Assessing prostate cancer risk: results from the Prostate Cancer Prevention Trial. J Natl Cancer Inst. 2006;98(8):529-534.

163. Song Y, Chavarro JE, Cao Y, et al. Whole milk intake is associated with prostate cancer-specific mortality among U.S. male physicians. J Nutr. 2013;143(2):189-196.

164. Llaverias G, Danilo C, Wang Y, et al. A Western-type diet accelerates tumor progression in an autochthonous mouse model of prostate cancer. Am J Pathol. 2010;177(6):3180-3191.

165. Quinn DI, Tangen CM, Hussain M, et al. Docetaxel and atrasentan versus docetaxel and placebo for men with advanced castration-resistant prostate cancer (SWOG S0421): a randomised phase 3 trial. Lancet Oncol. 2013;14(9):893-900.

166. National Comprehensive Cancer Network. NCCN Clinical Practice Guidelines in Oncology: Prostate Cancer. Version 2.2013. Available at http://www.nccn.org. Last accessed October 16, 2013.

167. Carroll P, Albertsen PC, Greene K, et al. PSA Testing for the Pretreatment and Posttreatment Management of Prostate Cancer, 2013: Revision of 2009 Best Practice Statement. Linthicum, MD: American Urological Association; 2013.

168. Sverrisson E, Jones JS, Pow-Sang JM. Cryosurgery for prostate cancer: a comprehensive review. Arch Esp Urol. 2013;66(6):546-556.

169. Ward JF, Diblasio CJ, Williams C, Given R, Jones JS. Cryoablation for locally advanced clinical stage T3 prostate cancer: a report from the Cryo-On-Line Database (COLD) Registry. BJU Int. 2013; [Epub ahead of print].

170. Working Group of the Clinical Practice Guideline on Prostate Cancer Treatment. Clinical Practice Guidelines on Prostate Cancer Treatment. Madrid: National Plan for the NHS of the MSC, Aragon Institute of Health Sciences; 2008.

171. Kelly WK, Halabi S, Carducci M, et al. Randomized, double-blind, placebo-controlled phase III trial comparing docetaxel and prednisone with or without bevacizumab in men with metastatic castration-resistant prostate cancer: CALGB 90401. J Clin Oncol. 2012;30(13):1534-1540.

172. Sheets NC, Goldin GH, Meyer AM, et al. Intensity-modulated radiation therapy, proton therapy, or conformal radiation therapy and morbidity and disease control in localized prostate cancer. JAMA. 2012;307(15):1611-1620.

Evidence-Based Practice Recommendations Citations

1. U.S. Preventive Services Task Force. Screening for prostate cancer: U.S. Preventive Services Task Force recommendation statement.Ann Intern Med. 2012;157(2):120-134. Summary retrieved from National Guideline Clearinghouse at http://www.guideline.gov/content.aspx?id=36923. Last accessed October 18, 2013.

2. Moran BJ, DeRose P, Merrick G, et al. ACR Appropriateness Criteria: Definitive External Beam Irradiation in Stage T1 and T2 Prostate Cancer. Reston, VA: American College of Radiology; 2010. Summary retrieved from National Guideline Clearinghouse at http://www.guideline.gov/content.aspx?id=32635. Last accessed October 18, 2013.

3. Prostate Cancer Clinical Guideline Update Panel. Guideline for the Management of Clinically Localized Prostate Cancer: 2007 Update. Linthicum, MD: American Urological Association Education and Research, Inc.; 2007. Summary retrieved from National Guideline Clearinghouse at http://www.guideline.gov/content.aspx?id=11446. Last accessed October 18, 2013.

4. Kramer BS, Hagerty KL, Justman S, et al. Use of 5-alpha-reductase inhibitors for prostate cancer chemoprevention: American Society of Clinical Oncology/American Urological Association 2008 Clinical Practice Guideline. J Clin Oncol. 2009;27(9):1502-1516. Summary retrieved from National Guideline Clearinghouse at http://www.guideline.gov/content.aspx?id=15227. Last accessed October 18, 2013.

Copyright © 2013 NetCE, P.O. Box 997571, Sacramento, CA 95899-7571
Mention of commercial products does not indicate endorsement.