Department of Clinical Pharmacology, College of Medicine and Public Health, and.
Department of Medical Oncology, Flinders Centre for Innovation in Cancer, Flinders Medical Centre/Flinders University, Bedford Park, South Australia, Australia.
J Natl Compr Canc Netw. 2020 Sep;18(9):1191-1199. doi: 10.6004/jnccn.2020.7567.
Immune-related adverse events (irAEs) are known to occur in patients with cancer who are treated with immune checkpoint inhibitors. However, limited literature exists on the incidence, time of onset, and risk factors for irAEs, particularly those affecting multiple organs, associated with anti-PD-L1 inhibitors.
A post hoc pooled analysis was conducted using individual patient data from atezolizumab monotherapy arms of 4 non-small cell lung cancer clinical trials. Incidence, clinical patterns, outcomes, and risk factors were investigated of selected organ-specific and multiorgan irAEs during treatment using the anti-PD-L1 inhibitor atezolizumab.
From a total of 1,548 patients, 730 irAE episodes were reported in 424 patients (27%). Skin irAEs were the most common (42%), followed by laboratory abnormalities (27%) and endocrine (11.6%), neurologic (7.6%), and pulmonary (6.2%) irAEs. A total of 84 patients (5.4%) had multiorgan irAEs, 70 had 2, 13 had 3, and 1 had 4 different organs affected. "Skin plus" or "laboratory plus" were the most common irAE multiorgan clusters. Patients with multiorgan irAEs were more likely to be white and have a good performance status, a lower baseline neutrophil-lymphocyte ratio, and a good or intermediate lung immune prognostic index score. Multiorgan irAEs were also associated with improved overall survival (hazard ratio, 0.47; 95% CI, 0.28-0.78; P<.0001) but not with progression-free survival (hazard ratio, 0.92; 95% CI, 0.62-1.35; P=.74) compared with the cohort with no irAEs.
Multiorgan irAEs occurred in 5.4% of patients treated with atezolizumab in non-small cell lung cancer trials. Future trials should consider routine reporting of data on multiorgan toxicities in addition to organ-specific toxicities.
免疫相关不良反应(irAEs)已知发生在接受免疫检查点抑制剂治疗的癌症患者中。然而,关于 irAEs 的发生率、发病时间和风险因素的文献有限,特别是与抗 PD-L1 抑制剂相关的影响多个器官的 irAEs。
使用来自四项非小细胞肺癌临床试验中单用阿替利珠单抗治疗臂的个体患者数据进行了一项事后汇总分析。使用抗 PD-L1 抑制剂阿替利珠单抗,在治疗期间对选定的器官特异性和多器官 irAEs 的发生率、临床模式、结局和风险因素进行了调查。
在总共 1548 名患者中,424 名患者(27%)报告了 730 次 irAE 发作。皮肤 irAEs 最常见(42%),其次是实验室异常(27%)和内分泌(11.6%)、神经(7.6%)和肺部(6.2%)irAEs。共有 84 名患者(5.4%)患有多器官 irAEs,70 名患者有 2 个,13 名患者有 3 个,1 名患者有 4 个不同的器官受累。“皮肤加”或“实验室加”是最常见的 irAE 多器官聚类。患有多器官 irAEs 的患者更可能是白人,且表现状态良好,基线中性粒细胞-淋巴细胞比值较低,肺部免疫预后指数评分良好或中等。多器官 irAEs 也与改善的总生存相关(风险比,0.47;95%CI,0.28-0.78;P<.0001),但与无 irAEs 的队列相比,无进展生存无差异(风险比,0.92;95%CI,0.62-1.35;P=.74)。
在非小细胞肺癌试验中,接受阿替利珠单抗治疗的患者中有 5.4%发生多器官 irAEs。未来的试验应考虑除器官特异性毒性外,还应常规报告多器官毒性的数据。