Internal Medicine Residency Program, University of Calgary, Calgary, AB T2N 4N1, Canada.
Cross Cancer Institute, University of Alberta, Edmonton, AB T2S 3C3, Canada.
Curr Oncol. 2023 Dec 9;30(12):10396-10407. doi: 10.3390/curroncol30120757.
The PACIFIC trial led to a new standard of care for patients with locally advanced lung cancer, but real-world practice has demonstrated that immune checkpoint inhibitor (ICI) pneumonitis can lead to significant clinical complications. This study aimed to examine the clinical predictors, outcomes, and healthcare utilization data in patients who received consolidation durvalumab. Using the Alberta Immunotherapy Database, NSCLC patients who received durvalumab in Alberta, Canada, from January 2018 to December 2021 were retrospectively evaluated. We examined incidence and predictive values of severe pneumonitis, with overall survival (OS) and time-to-treatment failure (TTF) using exploratory multivariate analyses. Of 189 patients, 91% were ECOG 0-1 and 85% had a partial response from chemoradiation prior to durvalumab. Median TTF and OS were not reached; 1-year OS was 82%. An amount of 26% developed any grade of pneumonitis; 9% had ≥grade 3 pneumonitis. Male gender and a pre-existing autoimmune condition were associated with severe pneumonitis. V20 was associated with any grade of pneumonitis. Pneumonitis development was found to be an independent risk factor for worse OS ( = 0.038) and TTF ( = 0.007). Our results suggest clinical and dosimetric predictive factors of durvalumab-associated pneumonitis. These results affirm the importance of careful patient selection for safe completion of consolidation durvalumab in real-world LA-NSCLC population.
PACIFIC 试验为局部晚期肺癌患者带来了新的治疗标准,但实际情况表明,免疫检查点抑制剂(ICI)性肺炎可能导致严重的临床并发症。本研究旨在探讨接受巩固性 durvalumab 治疗的患者的临床预测因素、结局和医疗保健利用数据。使用艾伯塔省免疫治疗数据库,回顾性评估了 2018 年 1 月至 2021 年 12 月在加拿大艾伯塔省接受 durvalumab 治疗的非小细胞肺癌(NSCLC)患者。我们研究了严重肺炎的发生率和预测值,以及使用探索性多变量分析的总生存率(OS)和治疗失败时间(TTF)。在 189 例患者中,91%的患者 ECOG 评分为 0-1,85%的患者在接受 durvalumab 治疗前接受了放化疗,有部分缓解。中位 TTF 和 OS 未达到;1 年 OS 为 82%。26%的患者发生任何级别的肺炎;9%的患者出现≥3 级肺炎。男性和预先存在的自身免疫性疾病与严重肺炎相关。V20 与任何级别的肺炎相关。肺炎的发生是 OS 更差( = 0.038)和 TTF 更差( = 0.007)的独立危险因素。我们的结果表明了 durvalumab 相关肺炎的临床和剂量预测因素。这些结果证实了在真实世界的局部晚期 NSCLC 人群中,为安全完成巩固性 durvalumab 治疗而仔细选择患者的重要性。