Department of Dermatology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Drexel University College of Medicine, Philadelphia, Pennsylvania.
JAMA Dermatol. 2024 Jul 1;160(7):741-745. doi: 10.1001/jamadermatol.2024.1420.
Masculinizing gender-affirming hormonal therapy is associated with the development of acne. While isotretinoin is a highly effective acne treatment, little is known about its effectiveness and safety among transgender and gender-diverse individuals receiving gender-affirming hormonal therapy.
To evaluate clinical outcomes of isotretinoin among transgender and gender-diverse individuals receiving gender-affirming hormonal therapy.
DESIGN, SETTING, AND PARTICIPANTS: This multicenter retrospective case series study was conducted at 4 medical centers: Mass General Brigham, University of Pennsylvania, Emory University, and Fenway Health. It included patients aged between 12 and 49 years who were receiving masculinizing gender-affirming hormonal therapy and prescribed isotretinoin for the management of acne between August 14, 2015, and September 20, 2023.
Isotretinoin therapy for the management of acne.
The percentage of patients experiencing improvement or clearance of acne, as well as rates of acne recurrence. Adverse effects and reasons for treatment discontinuation were also evaluated.
Among 55 included patients, the mean (SD) age was 25.4 years; 4 (7.3%) were Asian, 2 (3.6%) were Black, 4 (7.2%) were Hispanic, 1 was (1.8%) multiracial, and 36 (65.5%) were White. The median isotretinoin course duration was 6 months (IQR, 4.0-8.0), with a median cumulative dose of 132.7 mg/kg (IQR, 66.4-168.5); the cumulative dose was less than 90 mg/kg for 16 patients (29.1%) and less than 120 mg/kg for 22 patients (40.0%). Isotretinoin was associated with improvement in 48 patients (87.3%) and clearance in 26 patients (47.3%). For the 33 patients treated with a cumulative dose of 120 mg/kg or more, these rates increased to 32 patients (97.0%) and 21 patients (63.6%), respectively. Among the 20 patients who achieved acne clearance and had any subsequent health care encounters, the risk of recurrence was 20.0% (n = 4). The most frequently reported adverse effects were dryness (n = 44; 80.0%), joint pain (n = 8; 14.5%), and eczema (n = 5; 9.1%). Laboratory abnormalities were uncommon. Reasons for premature treatment discontinuation included cost, pharmacy issues, adverse effects, logistical reasons (scheduling), and wound healing concerns for gender-affirming surgery.
In this case series study of individuals with acne who were receiving masculinizing gender-affirming hormonal therapy and underwent isotretinoin treatment, isotretinoin was often effective and well tolerated. However, premature treatment discontinuation was common and associated with poorer outcomes. Further efforts are needed to understand optimal dosing and treatment barriers to improve outcomes in transgender and gender-diverse individuals receiving masculinizing gender-affirming hormonal therapy.
重要性:男性化性别肯定激素治疗与痤疮的发展有关。虽然异维 A 酸是一种非常有效的痤疮治疗方法,但对于接受性别肯定激素治疗的跨性别和性别多样化个体,其疗效和安全性知之甚少。
目的:评估接受性别肯定激素治疗的跨性别和性别多样化个体中异维 A 酸的临床疗效。
设计、地点和参与者:这是一项在 4 家医疗中心(马萨诸塞州综合医院、宾夕法尼亚大学、埃默里大学和芬威健康)进行的多中心回顾性病例系列研究。纳入年龄在 12 至 49 岁之间、正在接受男性化性别肯定激素治疗且在 2015 年 8 月 14 日至 2023 年 9 月 20 日期间因痤疮接受异维 A 酸治疗的患者。
暴露因素:异维 A 酸治疗痤疮。
主要结局和测量指标:评估患者痤疮改善或清除的比例,以及痤疮复发的发生率。还评估了不良反应和治疗中止的原因。
结果:在纳入的 55 名患者中,平均(SD)年龄为 25.4 岁;4 名(7.3%)为亚洲人,2 名(3.6%)为黑人,4 名(7.2%)为西班牙裔,1 名(1.8%)为多种族,36 名(65.5%)为白人。异维 A 酸疗程中位数为 6 个月(IQR,4.0-8.0),累积剂量中位数为 132.7mg/kg(IQR,66.4-168.5);16 名患者(29.1%)累积剂量小于 90mg/kg,22 名患者(40.0%)累积剂量小于 120mg/kg。异维 A 酸治疗后,48 名患者(87.3%)病情改善,26 名患者(47.3%)痊愈。对于接受累积剂量为 120mg/kg 或更高剂量治疗的 33 名患者,这些比例分别增加至 32 名(97.0%)和 21 名(63.6%)。在 20 名达到痤疮清除且有任何后续医疗就诊的患者中,复发风险为 20.0%(n=4)。最常报告的不良反应是干燥(n=44;80.0%)、关节痛(n=8;14.5%)和湿疹(n=5;9.1%)。实验室异常并不常见。提前停止治疗的原因包括费用、药房问题、不良反应、(日程安排)后勤问题和性别肯定手术的伤口愈合问题。
结论和相关性:在这项对接受男性化性别肯定激素治疗且接受异维 A 酸治疗的痤疮患者进行的病例系列研究中,异维 A 酸通常有效且耐受性良好。然而,提前停止治疗很常见,且与较差的结局相关。需要进一步努力了解最佳剂量和治疗障碍,以改善接受男性化性别肯定激素治疗的跨性别和性别多样化个体的结局。