Evidence map›Paper›PMID 41625007›Full record

ArticleInternational journal of transgender health2026

Bicalutamide does not raise transaminases clinically significantly compared to alternative anti-androgen regimens among transfeminine adolescents and young adults: A retrospective cohort study.

Katie Burgener, Brian DeBosch, Jinli Wang, Christopher Lewis, Cynthia Herrick

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Article in International journal of transgender health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Katie BurgenerDepartment of Pediatrics, Division of Endocrinology and Diabetes, Washington University in St. Louis, St. Louis, Missouri, USA.
Brian DeBoschDepartment of Pediatrics, Division of Gastroenterology, Hepatology and Nutrition, Indiana University, Bloomington, Indiana, USA.ORCID https://orcid.org/0000-0002-9924-7921
Jinli WangDepartment of Biostatistics, Washington University in St. Louis, St. Louis, Missouri, USA.
Christopher LewisDepartment of Pediatrics, Division of Endocrinology, University of Colorado, Denver, Colorado, USA.
Cynthia HerrickDepartment of Internal Medicine, Division of Endocrinology, Diabetes, and Lipid Metabolism Research, Washington University in St. Louis, St. Louis, Missouri, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Bicalutamide is a potential anti-androgen for transgender individuals with feminizing embodiment goals, but use is limited because of hepatotoxicity in cisgender men with prostate cancer. This study compared transaminase changes in transfeminine adolescents and young adults (AYA) using low dose bicalutamide with individuals using another androgen blockade. Methods: A retrospective analysis was conducted using electronic health record data for patients starting gender affirming hormone therapy with at least 10 months of follow-up between 2015 and 2023. The primary outcome was change in alanine aminotransferase (ALT) and aspartate aminotransferase (AST) from baseline. Linear mixed models compared change in ALT and AST from baseline and maximum ALT and AST values in bicalutamide and comparison groups. Secondary outcomes included % individuals with ALT and AST elevation more than 1, 2, or 3 times the upper limit of normal (ULN) (Fisher's exact test), standardized mean estradiol dose by group (t test), and Tanner staging of breast tissue by group (Fisher's exact test). Results: Eighty-four transfeminine AYA (median age 18) taking bicalutamide were compared to 69 transfeminine AYA (median age 19) taking GnRH agonists, spironolactone or no agent in addition to estradiol. In linear mixed models adjusted for baseline age, race, BMI, baseline ALT or AST, and alcohol use, there were no clinically significant differences in delta or maximum ALT or AST in bicalutamide and comparison groups. No individuals had AST or ALT levels > 3x ULN though % with AST > ULN was higher for bicalutamide (10.7 v 1.5%, Conclusion: Bicalutamide was not associated with a clinically significant change in transaminases as compared with other anti-androgen regimens over one year. Bicalutamide appears to be a safe anti-androgen for transfeminine individuals at low dose with close monitoring and deserves further study.

Indexed as

Adolescent and young adult (AYA)anti-androgenbicalutamidehepatotoxicitytransgender

Identifiers

PMID41625007
PMCPMC12857715

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.