Medical Oncology, Universitair Ziekenhuis Brussel.
Medical Oncology, Institut Jules Bordet, Brussels, Belgium.
Curr Opin Oncol. 2018 Mar;30(2):98-104. doi: 10.1097/CCO.0000000000000434.
The therapeutic armamentarium for advanced non-small-cell lung cancer has evolved considerably over the past years. Immune checkpoint inhibitors targeting programmed cell death-1 such as pembrolizumab and nivolumab or programmed cell death ligand 1 such as atezolizumab, durvalumab and avelumab have shown favorable efficacy results in this patient population in the first-line and second-line setting. These immunotherapies are associated with a distinct toxicity profile based on autoimmune organ toxicity which is a new challenge for supportive care during treatment with these drugs.
The differential diagnosis of events occurring during immune checkpoint inhibitor treatment is broad: they can be due to immune-related or nonimmune-related adverse events, atypical tumor responses (pseudoprogression or hyperprogression) or events related to comorbidities or other treatments.
The management of these patients includes a thorough baseline clinical, biological and radiologic evaluation, patient education, correct follow-up and management by a multidisciplinary team with a central role for the medical oncologist. Immune-related toxicities should be managed according to available guidelines.
近年来,晚期非小细胞肺癌的治疗手段有了显著发展。在一线和二线治疗中,针对程序性细胞死亡蛋白-1(如 pembrolizumab 和 nivolumab)或程序性细胞死亡配体 1(如 atezolizumab、durvalumab 和avelumab)的免疫检查点抑制剂显示出对这一患者群体有良好的疗效。这些免疫疗法与基于自身免疫器官毒性的独特毒性特征相关,这是治疗这些药物时支持性护理的新挑战。
免疫检查点抑制剂治疗期间发生的事件的鉴别诊断范围很广:它们可能是由于免疫相关或非免疫相关的不良事件、非典型的肿瘤反应(假性进展或超进展)或与合并症或其他治疗相关的事件。
这些患者的管理包括彻底的基线临床、生物学和影像学评估、患者教育、由多学科团队进行正确的随访和管理,其中医学肿瘤学家发挥核心作用。应根据现有指南来管理免疫相关毒性。