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寻常痤疮患者接受氯司特罗治疗后的下丘脑-垂体-肾上腺轴反应。

Hypothalamic-Pituitary-Adrenal Axis Response in Patients With Acne Vulgaris Treated With Clascoterone.

出版信息

J Drugs Dermatol. 2024 Jun 1;23(6):433-437. doi: 10.36849/JDD.7997.

Abstract

BACKGROUND

Clascoterone cream 1% is a topical androgen receptor inhibitor approved to treat acne vulgaris in patients =>12 years of age. This report provides details of patients who developed laboratory signs of hypothalamic-pituitary-adrenal (HPA) axis suppression without clinical signs of adrenal suppression during the clascoterone development program.

METHODS

Two open-label, multicenter, Phase 2 trials evaluated HPA axis suppression in patients with moderate-to-severe acne vulgaris. Study 1 (NCT01831960) enrolled cohorts of adults =>18 years of age and adolescents =>12 to <18 years of age. Study 2 (NCT02720627) enrolled adolescents 9 to <12 years of age. Patients applied clascoterone twice daily at maximum-exposure dosages for 14 days. Adrenal suppression was evaluated via cosyntropin stimulation test (CST) at baseline and day 14. Patients with an abnormal CST result (serum cortisol level =<18 µg/dL) had a follow-up CST approximately 4 weeks later. Blood was collected for pharmacokinetic analysis. Other safety assessments included adverse events (AEs), physical examination/vital signs, and electrocardiography.

RESULTS

Overall, 5/69 clascoterone-treated patients had an abnormal CST result on day 14, including 1/20 adults, 2/22 patients aged =>12 to <18 years, and 2/27 patients aged 9 to <12 years. All patients had normal cortisol levels at follow-up testing approximately 4 weeks later. No relationship was observed between abnormal CST results and clascoterone plasma concentrations or the amount of study drug applied. No clinically relevant AEs or clinically significant changes in safety measures were observed in patients with adrenal suppression.

CONCLUSION

Clascoterone induced laboratory evidence of mild, reversible HPA axis suppression under maximum-use exposure. J Drugs Dermatol. 2024;23(6):433-437.     doi:10.36849/JDD.7997.

摘要

背景

1%氯螺内酯乳膏是一种局部雄激素受体抑制剂,已被批准用于治疗 12 岁及以上患者的寻常痤疮。本报告详细介绍了在氯螺内酯开发项目期间,尽管没有肾上腺抑制的临床迹象,但出现了下丘脑-垂体-肾上腺 (HPA) 轴抑制的实验室迹象的患者情况。

方法

两项开放标签、多中心、2 期临床试验评估了中重度寻常痤疮患者的 HPA 轴抑制情况。研究 1(NCT01831960)招募了年龄≥18 岁的成年患者和年龄 12 至<18 岁的青少年患者。研究 2(NCT02720627)招募了年龄 9 至<12 岁的青少年患者。患者在最大暴露剂量下每天应用氯螺内酯两次,持续 14 天。在基线和第 14 天通过促皮质素刺激试验 (CST) 评估肾上腺抑制情况。CST 结果异常(血清皮质醇水平<18 µg/dL)的患者大约在 4 周后进行了随访 CST。采集血样进行药代动力学分析。其他安全性评估包括不良事件 (AE)、体格检查/生命体征和心电图。

结果

总体而言,69 例氯螺内酯治疗患者中有 5 例(1/20 例成年患者、2/22 例年龄>12 至<18 岁的患者和 2/27 例年龄 9 至<12 岁的患者)在第 14 天 CST 结果异常。所有患者在大约 4 周后的随访检测中皮质醇水平正常。在异常 CST 结果与氯螺内酯血浆浓度或研究药物使用量之间未观察到相关性。在有肾上腺抑制的患者中,未观察到与治疗相关的不良事件或安全性措施的临床显著变化。

结论

在最大使用暴露下,氯螺内酯引起了轻微、可逆的 HPA 轴抑制的实验室证据。皮肤病药物杂志。2024;23(6):433-437.

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