First Department of Medical Oncology, Chinese PLA General Hospital, Beijing, China.
Department of Graduate Administration, Chinese PLA General Hospital, Beijing, China.
Cancer Med. 2018 Aug;7(8):4115-4120. doi: 10.1002/cam4.1579. Epub 2018 May 23.
Immune checkpoint blockade-related pneumonitis is a rare but potentially life-threatening adverse effect, but its risk factors are not completely understood. This case-control study was conducted to identify pneumonitis risk factors in patients treated with anti-PD1 monoclonal antibodies (mAbs), including all the patients who developed pneumonitis after anti-PD-1 mAbs treatment in the Cancer Center of the Chinese People's Liberation Army from September 2015 to September 2017. Two controls per case were matched according to a propensity-score matching algorithm to account for confounding effects caused by individual baseline variables. Demographic and clinical information was obtained from medical records. In total, 55 cases and 110 controls were included in the study. No association was observed between smoking status or primary lung cancer and risk of pneumonitis. Significant risk factors for pneumonitis related to anti-PD-1 mAbs were prior thoracic radiotherapy, prior lung disease and combination therapy with odds ratios of 3.34 (1.51-7.39), 2.86 (1.45-5.64) and 2.73 (1.40-5.31), respectively. The associations remained significant in the multivariable logistic regression model. The risk of pneumonitis induced by anti-PD-1 mAbs is associated with prior thoracic radiotherapy, prior lung disease, and combination therapy. Clinicians should monitor these features in patients receiving anti-PD-1 therapy to optimize clinical safety and efficacy.
免疫检查点阻断相关肺炎是一种罕见但潜在致命的不良反应,但其危险因素尚未完全明确。本病例对照研究旨在确定接受抗 PD-1 单克隆抗体(mAb)治疗的患者发生肺炎的危险因素,包括 2015 年 9 月至 2017 年 9 月在中国人民解放军肿瘤中心接受抗 PD-1 mAb 治疗后发生肺炎的所有患者。采用倾向评分匹配算法,为每例病例匹配 2 例对照,以消除个体基线变量引起的混杂效应。从病历中获取人口统计学和临床信息。本研究共纳入 55 例病例和 110 例对照。吸烟状况或原发性肺癌与肺炎风险之间无相关性。与抗 PD-1 mAb 相关的肺炎的显著危险因素是既往胸部放疗、既往肺部疾病和联合治疗,比值比分别为 3.34(1.51-7.39)、2.86(1.45-5.64)和 2.73(1.40-5.31)。多变量逻辑回归模型中仍存在显著相关性。抗 PD-1 mAb 引起的肺炎风险与既往胸部放疗、既往肺部疾病和联合治疗相关。临床医生应在接受抗 PD-1 治疗的患者中监测这些特征,以优化临床安全性和疗效。