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Updated: Jun 1, 2026

A New Technique for Treating Low-risk Prostate Cancer—Super Active Surveillance
Published on: November 7, 2025
Targeting 5α-reductase for prostate cancer prevention and treatment
Lucas P Nacusi1, Donald J Tindall
1Department of Urology Research, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN 55905, USA.
Abstract:
Testosterone is the most abundant circulating androgen, and can be converted to dihydrotestosterone (DHT), a more potent androgen, by the 5α-reductase enzymes in target tissues. Current treatments for prostate cancer consist of reducing androgen levels by chemical or surgical castration or pure antiandrogen therapy that directly targets the androgen receptor (AR). Although these therapies reduce tumor burden and AR activity, the cancer inevitably recurs within 18-30 months. An approach targeting the androgen-AR axis at different levels could, therefore, improve the efficacy of prostate cancer therapy. Inhibition of 5α-reductase is one such approach; however, the two largest trials to investigate the use of the 5α-reductase inhibitors (5ARIs) finasteride and dutasteride in patients with prostate cancer have shown that, although the incidence of cancer was reduced by 5ARI treatment, those cancers that were detected were more aggressive than in patients treated with placebo. Thus, the best practice for using these drugs to prevent and treat prostate cancer remains unclear.
Insights
Androgen deprivation therapy is standard for prostate cancer, but resistance emerges. 5α-reductase inhibitors show promise in reducing cancer incidence but may increase aggressiveness, leaving optimal use unclear.
Area of Science:
- Oncology
- Endocrinology
- Urology
Background:
- Prostate cancer treatment relies on reducing androgens, like testosterone, and blocking the androgen receptor (AR).
- Current therapies often lead to inevitable cancer recurrence due to resistance mechanisms.
- Targeting the androgen-AR axis offers potential for improved prostate cancer management.
Purpose of the Study:
- To evaluate the role of 5α-reductase inhibitors (5ARIs) in prostate cancer prevention and treatment.
- To understand the impact of 5ARIs on prostate cancer aggressiveness.
Main Methods:
- Review of major clinical trials investigating 5α-reductase inhibitors (finasteride, dutasteride) in prostate cancer.
- Analysis of cancer incidence and tumor aggressiveness in patients treated with 5ARIs versus placebo.
Main Results:
- 5ARI treatment significantly reduced the overall incidence of prostate cancer.
- Detected prostate cancers in the 5ARI groups were more aggressive compared to the placebo group.
- The optimal clinical application of 5ARIs for prostate cancer remains undetermined.
Conclusions:
- While 5ARIs can decrease prostate cancer incidence, their effect on tumor aggressiveness requires careful consideration.
- Further research is needed to clarify the best practices for utilizing 5ARIs in prostate cancer prevention and therapy.
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