Jairam Vikram, Soulos Pamela R, K C Madhav, Gross Cary P, Slotman Ben J, Chiang Anne C, Park Henry S
Department of Radiation Oncology, Sutter Medical Group, Sacramento, California.
Cancer Outcomes, Public Policy and Effectiveness Research (COPPER) Center, Yale School of Medicine, New Haven, Connecticut.
Adv Radiat Oncol. 2023 Dec 3;9(4):101413. doi: 10.1016/j.adro.2023.101413. eCollection 2024 Apr.
The landmark randomized trial on chest irradiation in extensive disease small cell lung cancer (CREST) demonstrated that consolidative thoracic radiation therapy (cTRT) improved overall (OS) and progression-free survival (PFS) after initial chemotherapy (chemo) in extensive-stage small cell lung cancer, with potentially increased benefit in women compared with men. It is unknown whether similar findings would apply after chemoimmunotherapy became the standard first-line treatment. In this analysis, we report national practice patterns and survival outcomes of cTRT according to patient sex.
We included patients from de-identified electronic health record-derived database diagnosed with stage IV small cell lung cancer (2014-2021) who completed 4 to 6 cycles of first-line systemic therapy (platinum-doublet chemotherapy or chemoimmunotherapy). We evaluated OS and PFS using multivariable Cox proportional hazards regression with receipt of cTRT as an independent variable and stratified by sex. As a sensitivity analysis, we weighted the models by the inverse probability of receiving cTRT.
A total of 1227 patients were included (850 chemotherapy, 377 chemoimmunotherapy). There were no statistically significant differences in baseline characteristics between patients who did and did not receive cTRT. Among women, cTRT was associated with superior OS (adjusted hazard ratio [HR], 0.67; 95% CI, 0.52-0.87) and PFS (HR, 0.63; 95% CI, 0.49-0.82) compared with those not receiving cTRT. Conversely, no OS or PFS benefit with cTRT was observed in men (OS HR, 1.03; 95% CI, 0.80-1.31; PFS HR, 1.12; 95% CI, 0.85-1.47). Findings were similar in weighted analyses.
The survival efficacy of cTRT may be moderated by sex, with female patients appearing more likely to benefit than male patients. These findings reflect sex-based survival trends with similar effect sizes to those observed in the CREST trial. Although the underpinnings of this association need to be elucidated, stratification by sex should be considered for randomized-controlled trials studying cTRT in extensive-stage small cell lung cancer.
关于广泛期小细胞肺癌胸部放疗的里程碑式随机试验(CREST)表明,巩固性胸部放疗(cTRT)可改善广泛期小细胞肺癌初始化疗后的总生存期(OS)和无进展生存期(PFS),女性可能比男性获益更多。在化疗免疫疗法成为标准一线治疗后,类似的结果是否适用尚不清楚。在本分析中,我们报告了根据患者性别进行cTRT的全国实践模式和生存结果。
我们纳入了来自匿名电子健康记录衍生数据库的诊断为IV期小细胞肺癌(2014 - 2021年)且完成4至6周期一线全身治疗(铂类双联化疗或化疗免疫疗法)的患者。我们使用多变量Cox比例风险回归评估OS和PFS,将接受cTRT作为自变量并按性别分层。作为敏感性分析,我们用接受cTRT的逆概率对模型进行加权。
共纳入1227例患者(850例接受化疗,377例接受化疗免疫疗法)。接受和未接受cTRT的患者基线特征无统计学显著差异。在女性中,与未接受cTRT的患者相比,cTRT与更好的OS(调整后风险比[HR],0.67;95%置信区间,0.52 - 0.87)和PFS(HR,0.63;95%置信区间,0.49 - 0.82)相关。相反,在男性中未观察到cTRT对OS或PFS有获益(OS HR,1.03;95%置信区间;0.80 - 1.31;PFS HR,1.12;95%置信区间,0.85 - 1.47)。加权分析结果相似。
cTRT的生存疗效可能受性别影响,女性患者似乎比男性患者更可能获益。这些结果反映了基于性别的生存趋势,效应大小与CREST试验中观察到的相似。尽管这种关联的基础需要阐明,但在研究广泛期小细胞肺癌cTRT的随机对照试验中应考虑按性别分层。