Velcheti Vamsidhar, Moore Julia, Solem Caitlyn T
NYU (New York University) Langone Perlmutter Cancer Center, New York.
Currently affiliated with Mayo Clinic Florida, Jacksonville, Florida.
JAMA Netw Open. 2025 Jun 2;8(6):e2514527. doi: 10.1001/jamanetworkopen.2025.14527.
Effective treatments for advanced or metastatic non-small cell lung cancer (NSCLC) are limited. Understanding clinical treatment patterns is critical for understanding unmet medical needs.
To describe clinical treatment patterns and outcomes, including time to treatment discontinuation, progression-free survival, and overall survival, in patients who received platinum-based chemotherapy and anti-programmed cell death 1 protein or programmed cell death ligand 1 (PD-[L]1) regimens.
DESIGN, SETTING, AND PARTICIPANTS: This retrospective cohort study used data from 2018 to 2023 from a US nationwide, electronic health record-derived, deidentified database with median duration of follow-up of 7.8 (range, 0-65.0) months. Patients 18 years or older with advanced or metastatic NSCLC in second- and third-line treatment settings were included. Eligible patients had an Eastern Cooperative Oncology Group performance status of 0 or 1, received platinum-based chemotherapy and anti-PD-(L)1 therapy in 1 (combination) or 2 (sequential) lines, and initiated at least 1 subsequent treatment between January 1, 2018, and June 30, 2023. Exclusion criteria included disease progression within 8 weeks after anti-PD-(L)1 treatment initiation. Follow-up was until death or last available data through June 30, 2023.
Antineoplastic drugs following platinum-based chemotherapy and anti-PD-(L)1 treatment.
Time to treatment discontinuation, progression-free survival, and overall survival were analyzed overall and by initial treatment. Exploratory subgroup analyses were stratified by patient characteristics and index treatment without adjustment for group differences.
In the 1793 patients (974 [54.3%] male) included in the analysis, mean (SD) age at index treatment was 67.4 (9.4) years and median time from advanced diagnosis to index treatment was 10.5 (range, 1.1-103.8) months. The most common index treatments were docetaxel plus ramucirumab (314 [17.5%]), docetaxel monotherapy (158 [8.8%]), and carboplatin plus paclitaxel (136 [7.6%]). Overall, median time from index treatment to treatment discontinuation was 3.71 (95% CI, 3.48-3.94) months; median progression-free survival, 5.29 (95% CI, 5.03-5.52) months; and median overall survival, 11.20 (95% CI, 10.48-11.93) months. In exploratory analyses, these outcomes were numerically shorter in patients who received chemotherapy monotherapy as index treatment vs the overall group; medians were numerically longer in patients who received index treatments of immuno-oncology monotherapy or chemotherapy plus immuno-oncology combination therapy.
In this retrospective cohort study of patients with advanced or metastatic NSCLC, results underscored a significant need for novel treatments, including immuno-oncology combinations.
晚期或转移性非小细胞肺癌(NSCLC)的有效治疗方法有限。了解临床治疗模式对于理解未满足的医疗需求至关重要。
描述接受铂类化疗和抗程序性细胞死亡蛋白1或程序性细胞死亡配体1(PD-[L]1)方案的患者的临床治疗模式和结局,包括治疗中断时间、无进展生存期和总生存期。
设计、设置和参与者:这项回顾性队列研究使用了2018年至2023年来自美国全国性、源自电子健康记录且经过去识别处理的数据库的数据,中位随访时间为7.8(范围0 - 65.0)个月。纳入了年龄在18岁及以上、处于二线和三线治疗环境中的晚期或转移性NSCLC患者。符合条件的患者东部肿瘤协作组体能状态为0或1,在1(联合)或2(序贯)线治疗中接受铂类化疗和抗PD-(L)1治疗,并在2018年1月1日至2023年6月30日期间开始至少1次后续治疗。排除标准包括抗PD-(L)1治疗开始后8周内疾病进展。随访至死亡或截至2023年6月30日的最后可用数据。
铂类化疗和抗PD-(L)1治疗后的抗肿瘤药物。
总体及按初始治疗分析治疗中断时间、无进展生存期和总生存期。探索性亚组分析按患者特征和索引治疗进行分层,未对组间差异进行调整。
纳入分析的1793例患者(974例[54.3%]为男性),索引治疗时的平均(标准差)年龄为67.4(9.4)岁,从晚期诊断到索引治疗的中位时间为10.5(范围1.1 - 103.8)个月。最常见的索引治疗是多西他赛加雷莫西尤单抗(314例[17.5%])、多西他赛单药治疗(158例[8.8%])和卡铂加紫杉醇(136例[7.6%])。总体而言,从索引治疗到治疗中断的中位时间为3.71(95%置信区间,3.48 - 3.94)个月;中位无进展生存期为5.29(95%置信区间,5.03 - 5.52)个月;中位总生存期为11.20(95%置信区间,10.48 - 11.93)个月。在探索性分析中,接受化疗单药作为索引治疗的患者的这些结局在数值上短于总体组;接受免疫肿瘤学单药治疗或化疗加免疫肿瘤学联合治疗作为索引治疗的患者的中位数在数值上更长。
在这项针对晚期或转移性NSCLC患者的回顾性队列研究中,结果强调了对新型治疗方法(包括免疫肿瘤学联合疗法)的迫切需求。