Office of Clinical Pharmacology, FDA, Silver Spring, Maryland.
Syapse, San Francisco, California.
Cancer Res Commun. 2023 Feb 14;3(2):258-266. doi: 10.1158/2767-9764.CRC-22-0370. eCollection 2023 Feb.
Pneumonitis is a potentially life-threatening complication of anticancer therapy, and future treatment decisions may be informed by characterizing patients receiving therapies in the real-world setting. In this study, the incidence of treatment-associated pneumonitis (TAP) was compared among patients with advanced non-small cell lung cancer receiving immune checkpoint inhibitors (ICI) or chemotherapies in either of two settings: randomized clinical trials (RCT) or real world data (RWD)-based clinical practice. Pneumonitis cases were identified using International Classification of Diseases codes (for RWD), or the Medical Dictionary for Regulatory Activities preferred terms (for RCTs). TAP was defined as pneumonitis diagnosed during treatment or within 30 days of the last treatment administration. Overall TAP rates in the RWD cohort were lower [ICI: 1.9%; 95% confidence interval (CI), 1.2-3.2; chemotherapy: 0.8%; 95% CI, 0.4-1.6] than overall rates in the RCT cohort (ICI: 5.6%; 95% CI, 5.0-6.2; chemotherapy: 1.2%; 95% CI, 0.9-1.5). Overall RWD TAP rates were similar to grade 3+ RCT TAP rates (ICI: 2.0%; 95% CI, 1.6-2.3; chemotherapy: 0.6%; 95% CI, 0.4-0.9). In both cohorts, higher TAP incidence was observed among patients with a past medical history of pneumonitis than those without, regardless of treatment group. On the basis of this sizable study leveraging RWD, TAP incidence was low in the RWD cohort, likely in part due to methodology used for RWD focusing on clinically significant cases. Past medical history of pneumonitis was associated with TAP in both cohorts.
Pneumonitis is a potentially life-threatening complication of anticancer treatment. As treatment options expand, management decisions become increasingly complex, and there is a greater need to understand the safety profiles of the treatment options in the real-world setting. Real-world data serve as an additional source of valuable information to complement clinical trial data and inform understanding of toxicity in patients with non-small cell lung cancer receiving ICIs or chemotherapies.
肺炎是癌症治疗的一种潜在危及生命的并发症,通过描述在真实环境中接受治疗的患者,可以为未来的治疗决策提供信息。在这项研究中,比较了在接受免疫检查点抑制剂(ICI)或化疗的晚期非小细胞肺癌患者中,在以下两种环境下治疗相关肺炎(TAP)的发生率:随机临床试验(RCT)或基于真实世界数据(RWD)的临床实践。使用国际疾病分类代码(RWD)或监管活动医学词典首选术语(RCT)来识别肺炎病例。TAP 定义为在治疗期间或最后一次治疗给药后 30 天内诊断的肺炎。RWD 队列中的总体 TAP 发生率较低[ICI:1.9%;95%置信区间(CI),1.2-3.2;化疗:0.8%;95%CI,0.4-1.6],而 RCT 队列中的总体 TAP 发生率较高[ICI:5.6%;95%CI,5.0-6.2;化疗:1.2%;95%CI,0.9-1.5]。RWD 的总体 TAP 发生率与 RCT 的 3+级 TAP 发生率相似[ICI:2.0%;95%CI,1.6-2.3;化疗:0.6%;95%CI,0.4-0.9]。在两个队列中,无论治疗组如何,既往有肺炎病史的患者 TAP 发生率较高。在这项利用 RWD 的大型研究的基础上,RWD 队列中的 TAP 发生率较低,这可能部分归因于 RWD 中用于关注临床显著病例的方法。在两个队列中,既往肺炎病史与 TAP 相关。
肺炎是癌症治疗的一种潜在危及生命的并发症。随着治疗选择的扩大,管理决策变得越来越复杂,因此越来越需要了解在真实环境中接受 ICI 或化疗的非小细胞肺癌患者的治疗选择的安全性概况。真实世界的数据是补充临床试验数据和了解接受免疫检查点抑制剂或化疗的非小细胞肺癌患者毒性的另一个有价值的信息来源。