Oncology Department, Catalan Institute of Oncology, Hospital Universitari Doctor Josep Trueta, 17007 Girona, Spain.
Dermatology Department, Hospital Universitari Doctor Josep Trueta, 17007 Girona, Spain.
Curr Oncol. 2023 Aug 23;30(9):7802-7809. doi: 10.3390/curroncol30090566.
Cutaneous immune-related adverse events (cirAEs) are the most common side effects of immune checkpoint inhibitor (ICI) therapy (30-50% for all grades). The vast majority of them are low or mild and can be treated without ICI interruption. Autoimmune blistering disorders, such as immune-mediated bullous pemphigoid (IBP), are rare (<1%) but potentially serious conditions that must be early detected. The onset generally occurs within the first months of the treatment, and it appears to be more common with antiprogrammed death-1 or antiprogrammed ligand 1 (anti-PD1/PDL1) than with anticytotoxic T-lymphocyte-associated protein 4 (anti-CTLA4). We present a case of a three-day severe IBP onset after receiving the first cycle of atezolizumab. This exceptional early presentation could suggest the presence of some predisposing condition and demonstrates the need to better understand predictive toxicity-related biomarkers in candidate patients for immunotherapy.
皮肤免疫相关不良事件(cirAEs)是免疫检查点抑制剂(ICI)治疗中最常见的副作用(所有级别为 30-50%)。它们中的绝大多数为低或轻度,无需中断 ICI 治疗即可处理。自身免疫性大疱性疾病,如免疫介导的大疱性类天疱疮(IBP),则较为罕见(<1%),但却是必须早期发现的潜在严重病症。发病通常发生在治疗的最初几个月内,与抗程序性死亡受体 1 或抗程序性死亡配体 1(抗 PD1/PDL1)相比,与抗细胞毒性 T 淋巴细胞相关蛋白 4(抗 CTLA4)相比,似乎更为常见。我们报告了一例接受第一周期阿替利珠单抗治疗后三天出现严重 IBP 的病例。这种异常的早期表现可能表明存在一些易感条件,并证明需要更好地了解候选免疫治疗患者的毒性相关预测生物标志物。