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PMID: 19138953 Published · ppublish English Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural

Finasteride does not increase the risk of high-grade prostate cancer: a bias-adjusted modeling approach.

Cancer prevention research (Philadelphia, Pa.) ·Vol. 1 ·No. 3 ·2008-08-00 ·Pages 174-81

Redman MW, Tangen CM, Goodman PJ, Lucia MS, Coltman CA, Thompson IM

Abstract

Finasteride taken for 7 years in the Prostate Cancer Prevention Trial (PCPT) reduced the risk of prostate cancer by 25%, but with an apparent increased risk of high-grade disease. Subsequent analyses found that finasteride biases toward improved prostate cancer detection and accuracy in prostate cancer grading at biopsy. In our first analysis of the present study, we accounted for these biases in estimating the effect of finasteride on the risk of overall and high-grade prostate cancer. This analysis used PCPT data that included 3-month longer collection of endpoints than in the original report with observed prostate cancer rates of 22.9% (4.8% with high grade; placebo) versus 16.6% (5.8% with high grade; finasteride). Based on these updated results, the bias-adjusted prostate cancer rates are estimated to be 21.1% (4.2% high grade; placebo) and 14.7% (4.8% high grade; finasteride), a 30% risk reduction in prostate cancer [relative risk (RR), 0.70; 95% confidence interval (95% CI), 0.64-0.76; P < 0.0001] and a nonsignificant 14% increase in high-grade cancer (RR, 1.14; 95% CI, 0.96-1.35; P = 0.12) with finasteride. We then estimated rates of high-grade prostate cancer based on an analysis that incorporated grading information from radical prostatectomies in 500 subjects diagnosed with cancer. The resulting estimates were high-grade cancer rates of 8.2% (placebo) versus 6.0% (finasteride), a 27% risk reduction (RR, 0.73; 95% CI, 0.56-0.96; P = 0.02) with finasteride. Our third analysis examined the impact of biopsy sensitivity on the relative risk of high-grade prostate cancer and found that differential sensitivity of biopsy between the treatment arms can have a significant impact on risk ratio estimates. These collective results suggest that the observed, unadjusted higher risk of high-grade disease with finasteride seems to have been due to facilitated diagnosis resulting primarily from increased biopsy sensitivity with finasteride. Therefore, men undergoing regular prostate cancer screening or who express an interest in cancer prevention should be informed of the opportunity to take finasteride for preventing prostate cancer.

MeSH Terms
Aged Bias Biomarkers/analysis Biopsy Finasteride/therapeutic use Follow-Up Studies Humans Male Middle Aged Models, Statistical Neoplasm Staging Odds Ratio Placebos Prevalence Prostatectomy Prostatic Neoplasms/epidemiology,pathology,prevention & control,surgery Risk
Chemicals
Biomarkers Placebos Finasteride
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Redman Mary W
Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA. mredman@fhcrc.org
Tangen Catherine M
Goodman Phyllis J
Lucia M Scott
Coltman Charles A
Thompson Ian M
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12 references, click to expand
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Article Info
Journal
Cancer prevention research (Philadelphia, Pa.)
Abbr.
Cancer Prev Res (Phila)
ISSN
1940-6215
Published
2008-08-00
Epub
2008-00-18
Pages
174-81
Language
English
Region
United States
NLM ID
101479409
PMCID
PMC2844801
Subset
IM
Grants
NCI NIH HHS · U10 CA037429 · United States
NCI NIH HHS · U10 CA037429-21 · United States
NCI NIH HHS · CA37429 · United States
Corrections
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