Prostate-Specific Antigen Screening and Prostate Cancer Mortality: An Emulation of Target Trials in US Medicare

Author:

García-Albéniz Xabier12ORCID,Hsu John345,Etzioni Ruth6ORCID,Chan June M.78ORCID,Shi Joy19ORCID,Dickerman Barbra19ORCID,Hernán Miguel A.1910ORCID

Affiliation:

1. CAUSALab, Harvard T.H. Chan School of Public Health, Boston, MA

2. RTI Health Solutions, Barcelona, Spain

3. Mongan Institute, Massachusetts General Hospital, Boston, MA

4. Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA

5. Department of Health Care Policy, Harvard Medical School, Boston, MA

6. Fred Hutchinson Cancer Center, Seattle, WA

7. Department of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, CA

8. Department of Urology, University of California, San Francisco, San Francisco, CA

9. Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA

10. Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA

Abstract

PURPOSE No consensus about the effectiveness of prostate-specific antigen (PSA) screening exists among clinical guidelines, especially for the elderly. Randomized trials of PSA screening have yielded different results, partly because of variations in adherence, and it is unlikely that new trials will be conducted. Our objective was to estimate the effect of annual PSA screening on prostate cancer (PC) mortality in Medicare beneficiaries age 67-84 years. METHODS This is a large-scale, population-based, observational study of two screening strategies: annual PSA screening and no screening. We used data from 537,599 US Medicare (2001-2008) beneficiaries age 67-84 years who had a good life expectancy, no previous PC, and no PSA test in the 2 years before baseline. We estimated the 8-year PC mortality and incidence, treatments for PC, and treatment complications of PSA screening. RESULTS In men age 67-74 years, the estimated difference in 8-year risk of PC death between PSA screening and no screening was –2.3 (95% CI, –4.1 to –1.1) deaths per 1,000 men (a negative risk difference favors screening). Treatment complications were more frequent under PSA screening than under no screening. In men age 75-84 years, risk difference estimates were closer to zero. CONCLUSION Our estimates suggest that under conventional statistical criteria, annual PSA screening for 8 years is highly compatible with reductions of PC mortality from four to one fewer PC deaths per 1,000 screened men age 67-74 years. As with any study using real-world data, the estimates could be affected by residual confounding.

Publisher

American Society of Clinical Oncology (ASCO)

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