Division of Pharmaceutical Evaluation and Policy, College of Pharmacy, University of Arkansas for Medical Sciences, Little Rock, AR.
Department of Hematology and Medical Oncology, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR.
JCO Oncol Pract. 2023 Nov;19(11):1009-1019. doi: 10.1200/OP.23.00042. Epub 2023 Sep 20.
This study assessed real-world survival among older patients with non-small-cell lung cancer (NSCLC) and brain metastases (BMs) at diagnosis (synchronous BM [SBM]) receiving first-line immune checkpoint inhibitors (ICIs) compared with chemotherapy only.
Patients with NSCLC and SBM age 65 years or older at diagnosis from 2010 to 2019 SEER-Medicare database and received US Food and Drug Administration-approved ICIs (pembrolizumab/nivolumab/ipilimumab/atezolizumab/durvalumab/cemiplimab) and/or chemotherapy (platinum-based doublets/taxane/pemetrexed/gemcitabine) as first-line systemic treatment were included, excluding those with no cranial radiation or ever being treated with targeted therapies. Overall survival time was from the start of systemic treatment (ICI/chemotherapy) to death, censored at disenrollment from Medicare part A/B, enrollment in part C, or end of the study period (December 31, 2019). Kaplan-Meier (KM) survival curves were compared between treatment groups using the log-rank test. Multivariable Cox proportional hazards (CPH) model was used to estimate hazard ratio (HR) between groups, adjusting for patients' sociodemographic and clinical characteristics.
The study included 1,481 patients (1,303 chemotherapy and 178 ICI). The median (range) age was 71 (65-91) years. First-line ICI patients were more likely to be older, live in urban areas, and less likely to be non-White than the chemotherapy group. KM estimates showed that survival curves initially overlapped but diverged approximately 6 months after initiating first-line systemic treatment (median survival [95% CI]: ICI, 190 [131 to 303] days versus chemotherapy, 189 [177 to 201] days), with ICI showing a better survival than the chemotherapy group (log-rank test < .0001). First-line ICI was associated with a lower risk of death compared with chemotherapy in adjusted CPH model (HR [95% CI], 0.67 [0.55 to 0.80]; < .0001).
Among older patients with NSCLC and SBM, first-line ICI use was associated with improved survival occurring 6 months after treatment initiation compared with chemotherapy only.
本研究评估了在诊断时(同步脑转移 [SBM])接受一线免疫检查点抑制剂(ICI)治疗与单纯化疗相比,老年非小细胞肺癌(NSCLC)伴脑转移(BM)患者的真实世界生存情况。
本研究纳入了 2010 年至 2019 年 SEER-Medicare 数据库中年龄在 65 岁及以上、诊断时伴 SBM 的 NSCLC 患者,他们接受了美国食品和药物管理局(FDA)批准的 ICI(pembrolizumab/nivolumab/ipilimumab/atezolizumab/durvalumab/cemiplimab)和/或化疗(铂类双联/紫杉醇/培美曲塞/吉西他滨)作为一线全身治疗,排除了未行颅部放疗或曾接受过靶向治疗的患者。总体生存时间从全身治疗(ICI/化疗)开始至死亡,以从 Medicare 部分 A/B 中退出、加入部分 C 或研究结束(2019 年 12 月 31 日)为截止点。采用对数秩检验比较两组间的 Kaplan-Meier(KM)生存曲线。采用多变量 Cox 比例风险(CPH)模型估计组间危险比(HR),调整患者的社会人口统计学和临床特征。
本研究纳入了 1481 名患者(化疗组 1303 例,ICI 组 178 例)。中位(范围)年龄为 71(65-91)岁。与化疗组相比,一线 ICI 患者年龄更大,居住在城区,非白人患者比例更低。KM 估计显示,在开始一线全身治疗后大约 6 个月时,生存曲线最初重叠,但开始分离(中位生存时间 [95%CI]:ICI 组为 190[131 至 303]天,化疗组为 189[177 至 201]天),ICI 组的生存情况优于化疗组(对数秩检验<0.0001)。在调整后的 CPH 模型中,与化疗相比,一线 ICI 治疗与死亡风险降低相关(HR[95%CI],0.67[0.55 至 0.80];<0.0001)。
在老年 NSCLC 伴 SBM 患者中,与单纯化疗相比,在治疗开始后 6 个月时,一线 ICI 治疗可改善生存。