Division of Hospital Medicine, The Ohio State University, Columbus, OH, USA.
Division of Medical Oncology, The Ohio State University, 320 W 10th Ave, Columbus, OH, USA.
Cancer Immunol Immunother. 2020 Nov;69(11):2403-2408. doi: 10.1007/s00262-020-02674-w. Epub 2020 Jul 29.
Checkpoint inhibitor pneumonitis (CIP) is an immune-related adverse event that may complicate treatment with immune checkpoint inhibitors (ICI) and can cause significant morbidity. We sought to identify predictors for the development of CIP, and whether the use of inhaled corticosteroids (ICS) at time of ICI may be protective.
Patients with advanced cancer treated with ICI from 2011 and 2018 were included in this study. CIP attribution to ICI was determined by treating physician at time of diagnosis. Predictors were assessed by univariate and multivariable Cox proportional hazard models.
We identified 837 pts treated with ICI, of whom 30 (3.6%) developed grade 2 or higher CIP. 82 patients (9.8%) were receiving ICS at time of ICI and had increased risk of developing CIP with hazard ration (HR) of 4.22 (95% CI 1.93-9.21, p < 0.001) compared to those patients not receiving ICS. Patients with age ≥ 65 years had increased risk of developing CIP (HR 2.12, 95% CI 1.02-4.40, p = 0.044), as did 209 patients with lung cancer (198 NSCLC and 11 SCLC) compared to other types of cancers (HR 3.15, 95% CI 1.54-6.46, p = 0.002). In multivariable analysis, age ≥ 65 years, lung cancer diagnosis, and ICS use remained statistically associated with the development of CIP, with adjusted HR for ICS 3.09 (95% CI 1.32-7.24, p = 0.009).
Patients treated with ICS at time of ICI initiation had an increased risk of developing CIP. We further identified older adults with age ≥ 65 years and lung cancers as independent risk factors for CIP.
免疫检查点抑制剂相关性肺炎(CIP)是一种免疫相关的不良反应,可能使接受免疫检查点抑制剂(ICI)治疗的患者复杂化,并导致显著的发病率。我们旨在确定 CIP 发生的预测因素,以及 ICI 时使用吸入性皮质类固醇(ICS)是否具有保护作用。
本研究纳入了 2011 年至 2018 年期间接受 ICI 治疗的晚期癌症患者。ICI 相关肺炎的归因由诊断时的治疗医师确定。通过单变量和多变量 Cox 比例风险模型评估预测因素。
我们共纳入了 837 例接受 ICI 治疗的患者,其中 30 例(3.6%)发生 2 级或更高级别的 CIP。82 例(9.8%)患者在接受 ICI 的同时使用 ICS,与未使用 ICS 的患者相比,发生 CIP 的风险比(HR)为 4.22(95%CI 1.93-9.21,p<0.001)。年龄≥65 岁的患者发生 CIP 的风险增加(HR 2.12,95%CI 1.02-4.40,p=0.044),与其他类型癌症相比,肺癌(209 例非小细胞肺癌和 11 例小细胞肺癌)患者发生 CIP 的风险也更高(HR 3.15,95%CI 1.54-6.46,p=0.002)。多变量分析中,年龄≥65 岁、肺癌诊断和 ICS 使用与 CIP 的发生仍具有统计学关联,ICS 使用的调整 HR 为 3.09(95%CI 1.32-7.24,p=0.009)。
ICI 起始时使用 ICS 的患者发生 CIP 的风险增加。我们进一步发现,年龄≥65 岁的老年人和肺癌是 CIP 的独立危险因素。