Prostate cancer is the most diagnosed noncutaneous malignancy and the second most common cause of cancer death among men in the United States. Risk factors include older age, family history of prostate cancer, and Black race. Screening via prostate-specific antigen testing may lead to a small reduction in prostate cancer–specific mortality, with no reduction in all-cause mortality, but it can cause significant harms related to false-positive test results, unnecessary biopsies, overdiagnosis, and overtreatment. Shared decision-making is strongly recommended by all national guidelines before initiating screening. Most guidelines recommend screening every 2 to 4 years in men 55 to 69 years of age at average risk. After a positive prostate-specific antigen test result (more than 4 ng/mL), the test should be repeated. If the prostate-specific antigen level is still elevated, next steps include multiparametric magnetic resonance imaging, assessment of urine or blood biomarkers, and referral to urology. Active surveillance is increasingly accepted as the preferred standard of care for patients with newly diagnosed low-risk prostate cancer, because it is associated with similar long-term survival and better quality of life than curative treatment. The primary intent of screening is to identify patients with clinically significant prostate cancer who may benefit from curative treatment while minimizing the detection of clinically insignificant cancer.
Prostate cancer is the most diagnosed noncutaneous malignancy and the second most common cause of cancer death among men in the United States. There will be an estimated 299,010 prostate cancer diagnoses and 35,250 deaths from the condition in the United States in 2024.1
WHAT'S NEW ON THIS TOPIC: PROSTATE CANCER SCREENING

| The US Preventive Services Task Force analyzed three randomized controlled trials and estimated that for every 1,000 men 55 to 69 years of age screened with prostate-specific antigen testing over a 13-year period, 1.3 prostate cancer–related deaths would be prevented. None of the studies showed a reduction in all-cause mortality. |
| A meta-analysis estimated that for every 1,000 men screened with prostate-specific antigen testing compared with no screening over 10 years, further evaluation and treatment will result in 25 more men with erectile dysfunction, three more needing pads for urinary incontinence, and one more hospitalized with sepsis. |
| Patient decision aids can be an adjunct to shared decision-making about prostate-specific antigen screening by improving patient knowledge and decisional conflict and may decrease the number of men who decide to undergo screening (risk ratio = 0.88). |
SORT: KEY RECOMMENDATIONS FOR PRACTICE

PSA = prostate-specific antigen.
A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evidence; C = consensus, disease-oriented evidence, usual practice, expert opinion, or case series. For information about the SORT evidence rating system, go to https://www.aafp.org/afpsort.
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