Velcheti Vamsidhar, Sun Xuezheng, Hanna Maya, Zimmerman Nicole M, Singh Warsha K, Shah Manasee, Zhu Xinmei, Liao Anne, Altan Mehmet
Division of Hematology & Oncology, Mayo Clinic Comprehensive Cancer Center, Jacksonville, FL, USA.
Global Epidemiology, Oncology, GSK, Research Triangle, NC, USA.
Oncologist. 2025 Aug 4;30(8). doi: 10.1093/oncolo/oyaf070.
Real-world first-line maintenance (1LM) treatment data are limited for advanced/metastatic non-small cell lung cancer (a/mNSCLC).
In this electronic health record-derived, deidentified database study, eligible patients (≥18 years; diagnosed with stage III/IV non-small cell lung cancer [June 1, 2017-September 30, 2021]) initiated pembrolizumab-based 1LM after 4-6 cycles of first-line (1L) platinum-based chemotherapy-pembrolizumab ± pemetrexed. Study outcomes were real-world time to next treatment or death (rwTTNTD), overall survival (rwOS), and predictors of outcomes.
Of 1944 patients analyzed (median follow-up, 12.2 months), 51.9% received 1LM pembrolizumab-pemetrexed and 48.1% pembrolizumab monotherapy. Median rwTTNTD and rwOS were 9.2 (95% CI: 8.5-9.8) and 18.7 (95% CI: 17.7-20.3) months, respectively. In multivariable analyses, factors significantly associated with shorter rwTTNTD included 5%-<10% (hazard ratio [HR], 1.34; 95% CI: 1.17-1.54) or ≥10% (HR, 1.69; 95% CI: 1.42-2.01) weight loss during 1L versus 0% or <5% weight loss. Programmed death-ligand 1 (PD-L1) expression 1%-49% (HR, 0.81; 95% CI: 0.71-0.93) or ≥50% (HR, 0.55; 95% CI: 0.47-0.64) and female sex (HR, 0.85; 95% CI: 0.75-0.95) were significantly associated with longer rwTTNTD. These variables were also significantly associated with shorter (weight loss 5%-<10%: HR, 1.52; 95% CI: 1.30-1.77; ≥10% HR, 2.06; 95% CI: 1.71-2.48) and longer rwOS (PD-L1 expression: 1%-49% HR, 0.84; 95% CI: 0.72-0.98; ≥ 50% HR, 0.57; 95% CI: 0.48-0.68; female sex: HR, 0.81; 95% CI: 0.71-0.92).
Predictors of real-world clinical outcomes included 1L treatment, weight loss, PD-L1 status, and sex. Poor outcomes persisted despite immunotherapy-based 1LM availability, revealing an unmet need in this population.
针对晚期/转移性非小细胞肺癌(a/mNSCLC)的真实世界一线维持(1LM)治疗数据有限。
在这项源自电子健康记录的、去识别化数据库研究中,符合条件的患者(≥18岁;2017年6月1日至2021年9月30日期间被诊断为III/IV期非小细胞肺癌)在接受4 - 6周期一线(1L)铂类化疗 - 派姆单抗±培美曲塞后开始基于派姆单抗的1LM治疗。研究结局为真实世界下次治疗或死亡时间(rwTTNTD)、总生存期(rwOS)以及结局的预测因素。
在分析的1944例患者中(中位随访时间为12.2个月),51.9%接受1LM派姆单抗 - 培美曲塞治疗,48.1%接受派姆单抗单药治疗。rwTTNTD和rwOS的中位时间分别为9.2(95%置信区间:8.5 - 9.8)个月和18.7(95%置信区间:17.7 - 20.3)个月。在多变量分析中,与较短rwTTNTD显著相关的因素包括1L治疗期间体重减轻5% - <10%(风险比[HR],1.34;95%置信区间:1.17 - 1.54)或≥10%(HR,1.69;95%置信区间:1.42 - 2.01),而体重减轻0%或<5%则无此情况。程序性死亡配体1(PD - L1)表达为1% - 49%(HR,0.81;95%置信区间:0.71 - 0.93)或≥50%(HR,0.55;95%置信区间:0.47 - 0.64)以及女性(HR,0.85;95%置信区间:0.75 - 0.95)与较长rwTTNTD显著相关。这些变量也分别与较短(体重减轻5% - <10%:HR,1.52;95%置信区间:1.30 - 1.77;≥10% HR,2.06;95%置信区间:1.71 - 2.48)和较长rwOS(PD - L1表达:1% - 49% HR,0.84;95%置信区间:0.72 - 0.98;≥50% HR,0.57;95%置信区间:0.48 - 0.68;女性:HR,0.81;95%置信区间:0.71 - 0.92)显著相关。
真实世界临床结局的预测因素包括1L治疗、体重减轻、PD - L1状态和性别。尽管有基于免疫疗法的1LM治疗方案,但不良结局仍然存在,这揭示了该人群中未满足的需求。