Safety of 5α-Reductase Inhibitors and Spironolactone in Breast Cancer Patients Receiving Endocrine Therapies

    Raquel Rozner, Azael Freites-Martínez, Jerry Shapiro, Eliza B. Geer, Shari Goldfarb, Mario E. Lacouture
    Image of study
    TLDR The medications 5α-reductase inhibitors and spironolactone are generally safe for breast cancer patients on endocrine therapies and do not significantly increase breast cancer risk.
    The review, which included 47 studies from January 1978 through April 2018, aimed to evaluate the safety of 5α-reductase inhibitors and spironolactone in breast cancer patients on endocrine therapies. It found that 5α-reductase inhibitors did not consistently affect serum estrogen levels in 284 female patients, with 34% showing increased levels, 5.3% decreased, and 57% no change. Similarly, spironolactone did not consistently affect estrogen levels in 95 female patients, with 26% increased, 6.3% decreased, and 67% no change. Additionally, no increased breast cancer risk was observed in 49,298 patients taking spironolactone across three studies. The review concluded that spironolactone does not significantly increase breast cancer risk and could be considered for further research on alopecia and hirsutism in breast cancer patients. However, the efficacy of finasteride for treating female androgenetic alopecia remains controversial, and it is not recommended for women with endocrine therapy-induced alopecia until more is known about its long-term implications. Spironolactone may be a relatively safe systemic treatment option for managing EIA in female breast cancer patients and survivors.
    Discuss this study in the Community →

    Research cited in this study

    75 / 75 results

    Related Community Posts Join

    6 / 90 results
      FCE 28260: A Forgotten 5α-Reductase Inhibitor

      community FCE 28260: A Forgotten 5α-Reductase Inhibitor

      in Research  330 upvotes 2 months ago
      FCE 28260 (PNU 156765), an under-explored 5α-reductase inhibitor, showcases promising results in research by Giudici et al., outperforming well-known treatments like Finasteride in reducing the conversion of testosterone to DHT. Its superior efficacy, demonstrated through lower IC50 values in both natural and human recombinant enzyme studies, suggests it could offer more effective management of DHT-related conditions. Additionally, its lower molecular weight hints at better potential for topical application, potentially offering advantages in treating conditions such as androgenic alopecia. Despite its potential, it has not advanced in development, possibly due to financial limitations, leaving its therapeutic prospects and side effect profile largely unexplored.

      community NW5 at 19. How many grafts do I need?

      in Transplants  140 upvotes 1 year ago
      A 19-year-old with rapid hair loss since 16 is considering a hair transplant but refuses to take finasteride or any 5α-Reductase inhibitors. They are currently using minoxidil, tretinoin, and microneedling with a Derminator 2, and only want hair until age 27.

    Related Research

    2 / 2 results