Department of Pharmacoepidemiology, Graduate School of Medicine and Public Health, Kyoto University, Yoshida-Konoe-cho, Sakyo-ku, Kyoto, 606-8501, Japan.
Department of Clinical Epidemiology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, 852-8521, Japan.
Cancer Immunol Immunother. 2023 Mar;72(3):591-598. doi: 10.1007/s00262-022-03281-7. Epub 2022 Aug 22.
Chemotherapy for non-small cell lung cancer (NSCLC) patients with preexisting interstitial lung diseases (ILDs) increases the risk of developing pneumonitis. However, the association between pneumonitis and immune checkpoint inhibitors (ICIs) and related factors remains unclear.
We conducted a retrospective cohort study using a nationwide inpatient database. We included patients (aged ≥ 20 years) newly diagnosed with ILD and NSCLC and who started chemotherapy (ICIs or conventional chemotherapy) between January 2016 and December 2019. The primary endpoint was the onset of pneumonitis. We estimated the cumulative incidence function of pneumonitis and compared it with patients taking ICIs and patients receiving conventional chemotherapy using Gray's test. We calculated the subdistribution hazard ratios (HRs) and 95% confidence intervals (CIs) for the incidence of pneumonitis using Fine and Gray's model to adjust for sex, age, smoking status, histology of NSCLC, surgical history, and medical histories, considering death as the competing risk.
We identified 1177 patients (mean age 72 years, 13.8% female), of which 328 and 849 were in the ICI and conventional chemotherapy groups, respectively. There was no significant difference in the cumulative incidence function of pneumonitis between the two groups (p = 0.868). The adjusted subdistribution HR for the incidence of pneumonitis was 1.08 (95% CI: 0.74-1.57). Age (≥ 65 years) (HR: 1.86, 95% CI: 1.11-3.10) and smoking history (HR: 2.04, 95% CI: 1.02-4.11) were associated with developing pneumonitis.
The risk of developing pneumonitis with ICIs for NSCLC patients with preexisting ILD was similar to that with conventional chemotherapy.
患有间质性肺疾病(ILD)的非小细胞肺癌(NSCLC)患者进行化疗会增加发生肺炎的风险。然而,肺炎与免疫检查点抑制剂(ICIs)之间的关联及其相关因素仍不清楚。
我们使用全国性住院患者数据库进行了一项回顾性队列研究。我们纳入了在 2016 年 1 月至 2019 年 12 月期间新诊断为 ILD 和 NSCLC 且开始化疗(ICI 或常规化疗)的患者(年龄≥20 岁)。主要终点是肺炎的发病情况。我们估计了肺炎的累积发病率函数,并使用 Gray 检验比较了接受 ICI 治疗的患者、接受常规化疗的患者。我们使用 Fine 和 Gray 模型计算了肺炎发病的亚分布风险比(HR)和 95%置信区间(CI),以调整性别、年龄、吸烟状况、NSCLC 组织学、手术史和病史,将死亡视为竞争风险。
我们确定了 1177 名患者(平均年龄 72 岁,13.8%为女性),其中 328 名和 849 名患者分别在 ICI 组和常规化疗组。两组肺炎累积发病率函数无显著差异(p=0.868)。肺炎发病的调整后亚分布 HR 为 1.08(95%CI:0.74-1.57)。年龄(≥65 岁)(HR:1.86,95%CI:1.11-3.10)和吸烟史(HR:2.04,95%CI:1.02-4.11)与肺炎的发生有关。
对于患有预先存在的 ILD 的 NSCLC 患者,使用 ICI 治疗的肺炎发生风险与常规化疗相似。