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免疫检查点抑制剂诱导的孤立上腺皮质激素缺乏症:一个系统性审查
Fen Wang1, Xiaoli Shi1, Xuefeng Yu1
1Division of Endocrinology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Branch of National Clinical Research Center for Metabolic Diseases, Wuhan, China.
Frontiers in endocrinology
|February 6, 2024
概括
免疫检查点抑制剂诱导的孤立上腺皮质激素缺乏症 (IAD) 是一种罕见但严重的疾病,主要影响PD-1/PD-L1抑制剂的老年男性. 早期识别是关键,因为它可以无症状或存在非特异性症状.
科学领域:
- 内分泌学 在内分泌学.
- 在瘤学瘤学.
- 免疫学 免疫学 免疫学
背景情况:
- 免疫检查点抑制剂 (ICI) 可以导致罕见但危及生命的内分泌不良事件.
- 免疫检查点抑制剂诱导的孤立上腺皮质激素缺乏症 (IAD) 是接受癌症免疫治疗的患者的一个重大问题.
研究的目的:
- 系统地审查和表征免疫检查点抑制剂诱导的隔离腺皮质上腺激素缺乏症.
- 确定患者的人口统计,治疗模式,临床表现和与ICI诱导的IAD相关的结果.
主要方法:
- 在PubMed数据库中进行全面的文献搜索.
- 对免疫检查点抑制剂诱导的单独上腺皮质激素缺乏症病例的系统审查.
- 纳入标准要求明确提到其他前垂体激素状态.
主要成果:
- 确定了123例ICI诱导的IAD,主要在老年男性 (64.3±12.6岁) 中.
- 大多数患者接受了抗PD-1或抗PD-L1抗体;疲劳和食欲丧失是常见的症状.
- 报告了两例无症状病例; IAD 很少导致 ICI 停药或死亡.
结论:
- 由ICI诱导的IAD主要影响使用PD-1/PD-L1抑制剂的老年男性.
- 非特异性症状和无症状病例可能会延迟IAD的识别.
- 虽然潜在严重,但IAD通常不需要停止ICI,并且可以管理.
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