Immune checkpoint inhibitors as subsequent treatment in older adults with non-small cell lung cancer and synchronous brain metastases

被引:0
作者
Mahashabde, Ruchira, V [1 ]
Bhatti, Sajjad A. [2 ]
Martin, Bradley C. [1 ]
Painter, Jacob T. [1 ]
Rodriguez, Analiz [3 ]
Ying, Jun [4 ]
Li, Chenghui [1 ]
机构
[1] Univ Arkansas Med Sci, Coll Pharm, Div Pharmaceut Evaluat & Policy, 4301 West Markham St Slot 522, Little Rock, AR 72205 USA
[2] Univ Arkansas Med Sci, Coll Med, Dept Internal Med, Div Hematol & Med Oncol, Little Rock, AR 72205 USA
[3] Univ Arkansas Med Sci, Dept Neurosurg, Little Rock, AR 72205 USA
[4] Univ Arkansas Med Sci, Dept Biostat, Little Rock, AR 72205 USA
关键词
Immune checkpoint inhibitors (ICIs); older adults; non-small cell lung cancer (NSCLC); subsequent treatment; brain metastasis (BM); ELDERLY-PATIENTS; OPEN-LABEL; DOCETAXEL; SURVIVAL; OUTCOMES; NSCLC; PEMBROLIZUMAB; ATEZOLIZUMAB; NIVOLUMAB;
D O I
10.21037/tlcr-24-205
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Immune checkpoint inhibitors (ICIs) have become the mainstay treatment for non-small cell lung cancer (NSCLC). However, there is a lack of studies assessing ICIs as subsequent treatment in older adults with NSCLC and brain metastasis (BM). This retrospective cohort study compared the real-world survival of older patients with NSCLC and BM at diagnosis [synchronous BM (SBM)] previously treated with chemotherapy receiving ICI versus chemotherapy as subsequent treatment. Methods: Patients with NSCLC and SBM >= 65 years previously treated with chemotherapy were identified using the SEER-Medicare database (2010-2019). Patients receiving new chemotherapy and/or Food and Drug Administration (FDA)-approved ICIs as second/third-line treatment were included, excluding those ever-receiving targeted therapies. Each ICI patient was matched to one chemotherapy patient by time to subsequent treatment (within +/- 30 days) from diagnosis. Overall survival (OS) time was measured from the start of subsequent treatment to death, censored at disenrollment from Medicare Part A/B, enrollment in Part C, or end of study (December 31, 2019), whichever came first. OS curves were estimated and compared using the Kaplan-Meier (KM) method and log-rank test. Hazard ratio (HR) was estimated using a multivariable-adjusted Cox proportional hazards model. Results: Matched cohorts included 546 patients [273 in each group; median age 71 (range, 65-87) years]. ICI patients were older, more likely non-Hispanic, with squamous cell carcinoma, and liver metastasis compared to chemotherapy. KM estimated better survival in ICI than chemotherapy {median survival: 209 days [95% confidence interval (CI): 160-275] vs. 155 days (95% CI: 135-187); log-rank P<0.001}. ICI was associated with a lower adjusted hazard of death [HR =0.63; 95% CI: 0.52-0.75; P<0.001] compared to subsequent chemotherapy treatment. Conclusions: In this population-based study of older patients with NSCLC and SBM previously treated with chemotherapy, subsequent treatment with ICI was associated with improved survival compared to chemotherapy.
引用
收藏
页码:1620 / 1634
页数:21
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