Effect of Dutasteride on the Risk of Prostate Cancer

Dutasteride, an inhibitor of 5α-reductase in the prostate, was tested in a large, randomized trial to determine its ability to prevent prostate cancer. Over the 4 years of the trial, dutasteride, as compared with placebo, reduced the relative risk of biopsy-detected prostate cancer by 23%. The reduc...

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Veröffentlicht in:NEW ENGLAND JOURNAL OF MEDICINE 2010-04, Vol.362 (13), p.1192-1202
Hauptverfasser: Andriole, Gerald L, Bostwick, David G, Brawley, Otis W, Gomella, Leonard G, Marberger, Michael, Montorsi, Francesco, Pettaway, Curtis A, Tammela, Teuvo L, Teloken, Claudio, Tindall, Donald J, Somerville, Matthew C, Wilson, Timothy H, Fowler, Ivy L, Rittmaster, Roger S
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Sprache:eng
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Zusammenfassung:Dutasteride, an inhibitor of 5α-reductase in the prostate, was tested in a large, randomized trial to determine its ability to prevent prostate cancer. Over the 4 years of the trial, dutasteride, as compared with placebo, reduced the relative risk of biopsy-detected prostate cancer by 23%. The reduction was limited mainly to tumors with Gleason scores of 5 or 6; by year 4, there were 12 tumors with Gleason scores of 8 to 10 in the dutasteride group but only 1 in the placebo group. Dutasteride, an inhibitor of 5α-reductase in the prostate, reduced the relative risk of biopsy-detected prostate cancer by 23%; however, the reduction was limited mainly to tumors with Gleason scores of 5 or 6. The 5α-reductase inhibitors that are used to treat benign prostatic hyperplasia block the conversion of testosterone to dihydrotestosterone and may reduce the risk of prostate cancer. 1 The results of the Prostate Cancer Prevention Trial showed that finasteride, as compared with placebo, reduced the risk of prostate cancer by 25%, but among the tumors that were detected, there was a 27% increase in the number of those that had Gleason scores of 7 to 10. 2 (The Gleason score is the sum of the two most common histologic patterns or grades in a prostate tumor, each of which is graded on a . . .
ISSN:0028-4793
1533-4406
1533-4406
DOI:10.1056/NEJMoa0908127