The effects of the dual 5α-reductase inhibitor dutasteride on localized prostate cancer -: Results from a 4-month pre-radical prostatectomy study

BACKGROUND. As dihydrotestosterone (DHT) is the most potent androgen in the prostate, inhibition of the 5 alpha-reductase isoenzymes, which convert testosterone to DHT, could be an appropriate target for the treatment of prostate cancer. METHODS. Eighty-one men with clinically localized prostate cancer received daily dutasteride 3.5 or 0.5 mg, or no therapy for 4 months before radical prostatectomy. Histopathological assessments were conducted on prostatectomy specimens. RESULTS. Treatment with dutasteride was associated with reductions in serum and intraprostatic DHT of >= 90%, and a decrease in total prostate and tumor volumes. No effect of dutasteride was noted on Gleason grade. Histopathological effects on benign tissue were similar but less prominent than those seen with androgen ablation, whereas there was no significant difference in cancer histology among the groups. CONCLUSIONS. Dutasteride treatment results in similar but less marked changes compared with androgen ablation.