Angus Lachlan M, Hong Quoc Vinh, Cheung Ada S, Nolan Brendan J
Trans Health Research Group, Department of Medicine, University of Melbourne, Parkville, VIC, Australia.
Department of Medicine, Northern Health, Epping, VIC, Australia.
Ther Adv Endocrinol Metab. 2024 Dec 16;15:20420188241305022. doi: 10.1177/20420188241305022. eCollection 2024.
There is interest in repurposing bicalutamide for gender-affirming hormone therapy, but little data regarding efficacy and safety in the transgender population.
To determine the effect of bicalutamide on serum total testosterone concentrations and liver function. Given bicalutamide is a pure androgen receptor antagonist, we hypothesized that serum total testosterone concentrations would be higher than the cisgender female reference range and those recommended for transgender individuals in consensus guidelines.
Case series.
We identified transgender people attending outpatient clinics who were using bicalutamide for gender affirmation. The primary outcome was serum total testosterone concentration. Secondary outcomes included serum alanine transferase (ALT) concentration.
Twenty-four transfeminine people prescribed bicalutamide were identified. The median (interquartile range) age was 29 (24-38) years, bicalutamide dose 25 (25-50) mg daily and bicalutamide duration 6 (4-10) months. The median serum total testosterone concentration was 7.7 (0.7-17.5) nmol/L, luteinizing hormone 2.9 (0.5-6.0) IU/L and ALT 20 (13-29) IU/L. One individual had asymptomatic transaminitis. Six individuals discontinued bicalutamide due to a lack of perceived benefit.
Bicalutamide was associated with significant variation in serum total testosterone concentration, likely related to concomitant estradiol or previous anti-androgen therapy. Median serum ALT concentrations remained within the normal reference range. Guideline recommendations for serum total testosterone within the cisgender female reference range may be inappropriate for people using bicalutamide. Further research is needed to establish the longer-term efficacy and safety of bicalutamide in the transfeminine population.
对于将比卡鲁胺重新用于性别肯定激素治疗存在一定兴趣,但关于其在跨性别群体中的疗效和安全性的数据很少。
确定比卡鲁胺对血清总睾酮浓度和肝功能的影响。鉴于比卡鲁胺是一种纯雄激素受体拮抗剂,我们假设血清总睾酮浓度会高于顺性别女性参考范围以及共识指南中为跨性别者推荐的范围。
病例系列研究。
我们识别出在门诊使用比卡鲁胺进行性别肯定治疗的跨性别者。主要结局是血清总睾酮浓度。次要结局包括血清丙氨酸转氨酶(ALT)浓度。
共识别出24名接受比卡鲁胺治疗的跨性别女性。中位(四分位间距)年龄为29(24 - 38)岁,比卡鲁胺剂量为每日25(25 - 50)mg,用药时间为6(4 - 10)个月。血清总睾酮浓度中位数为7.7(0.7 - 17.5)nmol/L,促黄体生成素为2.9(0.5 - 6.0)IU/L,ALT为20(13 - 29)IU/L。1例个体有无症状性转氨酶升高。6例个体因未感觉到益处而停用比卡鲁胺。
比卡鲁胺与血清总睾酮浓度的显著变化有关,可能与同时使用的雌二醇或既往抗雄激素治疗有关。血清ALT浓度中位数仍在正常参考范围内。对于使用比卡鲁胺的人群,将血清总睾酮浓度设定在顺性别女性参考范围内的指南建议可能并不合适。需要进一步研究以确定比卡鲁胺在跨性别女性群体中的长期疗效和安全性。