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Clinical Question
Can prostate-specific antigen–based risk-stratified screening decrease the screening burden without increased harms to men?
Bottom line
Using 2 computer models, these researchers found that screening men from age 45 years until age 69 years with prostate-specific antigen (PSA)–based risk-stratified screening (ie, less frequent screening if the baseline PSA is less than 1.0 ng/mL and no screening if the PSA is less than 1.0 ng/mL at 60 years of age) results in a marked reduction in the burdens of screening and fewer overdiagnoses at the expense of fewer lives saved compared with biennial screening. Recall that the prostate screening trials found no overall mortality improvements and tiny reductions in cancer-specific mortality, so these models definitely need real-world testing. 3b
Reference
Study design: Other
Funding: Government
Setting: Population-based
Synopsis
Screening for prostate cancer has been controversial for several reasons, some of which are directly related to balancing the potential benefits against the harms of screening. These researchers used 2 independently developed computer simulation models to evaluate the trade-offs of less frequent screening in men aged 45 or 50 years with a baseline PSA below 1.0 ng/mL and the cessation of screening altogether if the PSA is below 1.0 ng/mL in men 60 years of age. The idea of less frequent screening means fewer direct harms of pursuing false positive results and reducing overdiagnosis, but at the risk of (potentially) more cancers missed and more cancer deaths. The models used virtual populations in which individuals can develop prostate cancer and their cancers can progress. The authors also compared model performance with real-world data from the Malmo Preventive Project. The models started with virtual men 45 or 50 years of age and followed them up until age 85. The models evaluated several strategies: screening every 2 years until age 69; lengthening the screening interval to 8 years for a baseline PSA of less than 1.0 ng/mL but decreasing again to 2 years if a subsequent PSA is greater than 1.0 ng/mL; stopping screening when PSA is less than 1.0 ng/mL at age 60 years and older; or a combination of the last 2 strategies. Regardless of strategy, the models used PSA levels exceeding 4.0 ng/mL to trigger further investigation. The investigators found that the models reasonably replicated the PSA distributions seen in the real-world Malmo data. Using a base model, screening 10,000 men biennially from ages 45 to 69 would require more than 100,000 screens; one model would yield 277 overdiagnoses and the other would yield 348 overdiagnoses. Additionally, they would save 110 to 160 lives and gain 921 to 1312 life-years relative to no screening. Using the risk-based screening, the models predicted the number of screenings would nearly be cut in half (47% reduction) and the overdiagnoses reduced by 2.1% or 0.9%, respectively. However, the models also saw a small reduction in lives saved (3.8% and 3.1%, respectively). Additionally, stopping screening if the PSA was less than 1.0 ng/mL at 60 years of age or older decreased overdiagnoses (24.0% and 5.5% relative reductions, respectively) and lives saved (13.1% and 5.0% relative reductions, respectively).
Reviewer
Henry C. Barry, MD, MS
Professor
Michigan State University
East Lansing, MI
Comments
When less screening is better?
"Recall that the prostate screening trials found ... tiny reductions in cancer-specific mortality, so these models definitely need real-world testing"
psa
< 1.0 is good
Prostate screening
Very helpful in avoiding unnecessary intervention and all the anxiety that goes with it.
Shocking to see how large the over-treatment figures were.
psa screening
large Scandinavian studies in the past showed very low cancer rates in males > 60 with asa < 1.0
could screen less often or not at all, unless fh of prostate cancer