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黑色素瘤患者罕见的免疫相关不良事件:发生率、谱和临床表现。

Rare immune-related adverse events in patients with melanoma: incidence, spectrum, and clinical presentations.

机构信息

School of Medicine, Vanderbilt University, Nashville, TN, USA.

Melanoma Institute Australia, The University of Sydney, Sydney, Australia.

出版信息

Oncoimmunology. 2023 Mar 8;12(1):2188719. doi: 10.1080/2162402X.2023.2188719. eCollection 2023.

DOI:10.1080/2162402X.2023.2188719
PMID:36926262
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10012911/
Abstract

Immune-related adverse events (irAEs) are side effects of immune checkpoint inhibitor therapy (ICI). While common irAEs have been well characterized, there are more limited data on rare immune related adverse events (RirAEs) due to low incidence. Lack of characterization of these entities has led to difficulties in accurate diagnosis and management. Here, we conducted a multi-institution analysis of all patients with stage III/IV melanoma who developed RirAEs after being treated with ICIs (anti-PD-1/L1, anti-CTLA-4, and combination PD-1/CTLA-4 blockade) at three institutions (Vanderbilt University Medical Center, Massachusetts General Hospital, and Melanoma Institute of Australia). RirAEs were defined as those occurring in approximately <1% of patients treated with anti-PD-1 or <2% with combination. Of 2834 patients who received ICIs, 82 developed RirAEs and were more common with combination PD-1/CTLA-4 blockade (4.6%) vs. anti-PD-1/L1 agents (2.8%). Overall median time from ICI start to RirAE was 86 days (interquartile range 42-235 days) with significantly earlier onset in combination therapy ( < 0.001). The spectrum of RirAEs spanned across several organ systems. Most RirAEs were grade 2 (57 [41.3%]) and grade 3 (40 [29.0%]) with relatively few grade 4 (11 [8.0%]) or 5 (5 [3.6%]) events. Steroid re-escalation (21.4%) or additional immunosuppression (13.8%) were commonly required. RirAE recurrence occurred in 22.6% with ICI rechallenge; 37.1% had new irAEs with rechallenge. In conclusion, RirAEs associated with ICIs in melanoma patients occurred, in aggregate, in 2-5% of patients treated with anti-PD-1-based therapy. Steroid re-escalation and alternative immunosuppression use were frequently required but fatal irAEs were fairly uncommon.

摘要

免疫相关不良事件(irAEs)是免疫检查点抑制剂治疗(ICI)的副作用。虽然常见的 irAEs 已经得到了很好的描述,但由于发病率较低,关于罕见的免疫相关不良事件(RirAEs)的数据则更为有限。由于这些实体缺乏特征描述,导致准确诊断和管理变得困难。在这里,我们对在三家机构(范德比尔特大学医学中心、马萨诸塞州综合医院和澳大利亚黑色素瘤研究所)接受 ICI(抗 PD-1/L1、抗 CTLA-4 和 PD-1/CTLA-4 联合阻断)治疗的 III/IV 期黑色素瘤患者中发生 RirAEs 的所有患者进行了多机构分析。RirAEs 的定义为接受抗 PD-1 治疗的患者中约发生 <1%或接受联合治疗的患者中 <2%的不良事件。在接受 ICI 治疗的 2834 例患者中,有 82 例发生了 RirAEs,且联合 PD-1/CTLA-4 阻断(4.6%)比抗 PD-1/L1 药物(2.8%)更常见。从 ICI 开始到发生 RirAE 的中位时间为 86 天(四分位距 42-235 天),联合治疗的起始时间明显更早(<0.001)。RirAEs 的发生涉及多个器官系统。大多数 RirAEs 为 2 级(57[41.3%])和 3 级(40[29.0%]),相对较少为 4 级(11[8.0%])或 5 级(5[3.6%])事件。需要经常重新使用类固醇(21.4%)或增加免疫抑制(13.8%)。ICI 再挑战时 RirAE 复发率为 22.6%;再挑战时有 37.1%出现新的 irAEs。总之,在接受基于抗 PD-1 治疗的黑色素瘤患者中,ICI 相关的 RirAEs 总发生率为 2-5%。需要经常重新使用类固醇和其他免疫抑制剂,但致命的 irAEs 相当少见。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4250/10012911/646fc450bbd2/KONI_A_2188719_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4250/10012911/f0b9358a9adb/KONI_A_2188719_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4250/10012911/646fc450bbd2/KONI_A_2188719_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4250/10012911/f0b9358a9adb/KONI_A_2188719_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4250/10012911/646fc450bbd2/KONI_A_2188719_F0002_OC.jpg

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