Division of Pulmonary Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland.
J Thorac Oncol. 2019 Mar;14(3):494-502. doi: 10.1016/j.jtho.2018.11.016. Epub 2018 Nov 30.
With increasing use of immune checkpoint inhibitors (ICIs) for advanced NSCLC, there is increasing recognition of immune-related adverse events associated with ICI use. We recently reported increased incidence of checkpoint inhibitor pneumonitis (CIP) in ICI-treated NSCLC patients. Since development of immune-related adverse events in other organ systems has been associated with either no change or even improvement in tumor response/cancer outcomes, we sought to better understand the impact of CIP development on overall survival in ICI-treated NSCLC patients. Using baseline and follow-up data collected on a cohort of 205 ICI-treated NSCLC patients, we used a multi-state modeling approach to understand the effect of developing CIP on the risk of death. We observed time-dependent changes in risk of developing and recovery from CIP, with an increased risk of both developing and recovering from CIP in the first year after initiating ICI. We found that developing CIP independently increased the risk of transitioning to death in both adjusted and unadjusted models. In the multivariate model, we found that the increase in mortality associated with CIP was only seen in patients with adenocarcinoma tumor histology. Collectively, these findings suggest that in NSCLC, development of CIP worsens survival in patients receiving immunotherapy.
随着免疫检查点抑制剂(ICI)在晚期非小细胞肺癌(NSCLC)中的应用越来越多,人们越来越认识到与 ICI 使用相关的免疫相关不良事件。我们最近报道了在接受 ICI 治疗的 NSCLC 患者中,检查点抑制剂性肺炎(CIP)的发生率增加。由于其他器官系统中免疫相关不良事件的发展与肿瘤反应/癌症结果的无变化甚至改善有关,我们试图更好地了解 CIP 发展对接受 ICI 治疗的 NSCLC 患者总生存的影响。我们使用在 205 名接受 ICI 治疗的 NSCLC 患者队列中收集的基线和随访数据,使用多状态建模方法来了解 CIP 发展对死亡风险的影响。我们观察到 CIP 发展和恢复的风险随时间的变化,在开始 ICI 后的第一年,同时增加了 CIP 发展和恢复的风险。我们发现,CIP 的发展独立增加了在调整和未调整模型中向死亡转移的风险。在多变量模型中,我们发现 CIP 相关的死亡率增加仅见于腺癌肿瘤组织学的患者。总之,这些发现表明,在 NSCLC 中,CIP 的发展会使接受免疫治疗的患者的生存恶化。