Patient-reported outcomes in CodeBreaK 200: Sotorasib versus docetaxel for previously treated advanced NSCLC with KRAS G12C mutation

IF 4.5 2区 医学 Q1 ONCOLOGY Lung Cancer Pub Date : 2024-08-06 DOI:10.1016/j.lungcan.2024.107921
David M. Waterhouse , Sacha Rothschild , Christophe Dooms , Bertrand Mennecier , Farastuk Bozorgmehr , Margarita Majem , Michel H. van den Heuvel , Helena Linardou , Byoung Chul Cho , Rachel Roberts-Thomson , Kentaro Tanaka , Normand Blais , Gustavo Schvartsman , Karin Holmskov Hansen , Izabela Chmielewska , Martin D. Forster , Christina Giannopoulou , Björn Stollenwerk , Cynthia C. Obiozor , Yang Wang , Silvia Novello
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Abstract

Background

In the CodeBreaK 200 phase III, open-label trial, sotorasib significantly improved efficacy versus docetaxel in previously treated KRAS G12C-mutated advanced non-small cell lung cancer (NSCLC). Patient-reported outcomes (PROs) for global health status, physical functioning, dyspnea, and cough favored sotorasib over docetaxel. Here, we report sotorasib’s additional impact on quality of life (QOL).

Methods

In CodeBreaK 200, 345 patients who had progressed after prior therapy received sotorasib (960 mg orally daily) or docetaxel (75 mg/m2 intravenously every 3 weeks). Validated questionnaires captured patients’ perception of their QOL and symptom burden for key secondary and exploratory PRO endpoints, including the European Organisation for Research and Treatment of Cancer Quality-of-life Questionnaire Core 30 (EORTC QLQ-C30) and Quality-of-life Questionnaire Lung Cancer 13 (EORTC QLQ-LC13), question GP5 from the Functional Assessment of Cancer Therapy Tool General Form (FACT-G GP5), PRO-Common Terminology Criteria for Adverse Events (PRO-CTCAE), and 5-level EuroQOL-5 dimensions (EQ-5D-5L) including visual analog scale (EQ-5D VAS). Change from baseline to week 12 was assessed with generalized estimating equations for ordinal outcomes.

Results

Patients receiving sotorasib were less bothered by treatment side effects than those receiving docetaxel (odds ratio [OR] 5.7) and experienced symptoms at lower severity (pain: OR 2.9; aching muscles: OR 4.4; aching joints: OR 4.2; mouth or throat sores: OR 4.3). Further, patients’ symptoms interfered less with usual/daily activities (pain: OR 3.2; aching muscles: OR 3.9; aching joints: OR 10.7). QOL remained stable with sotorasib but worsened with docetaxel (change from baseline in EQ-5D VAS score: 1.5 vs –8.4 at cycle 1 day 5 and 2.2 vs –5.8 at week 12).

Conclusions

Patients receiving sotorasib reported less severe symptoms than those receiving docetaxel. In addition to improving clinical efficacy outcomes, sotorasib maintained QOL versus docetaxel, suggesting sotorasib may be a more tolerable treatment option for patients with pretreated, KRAS G12C-mutated advanced NSCLC.

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CodeBreaK 200的患者报告结果:索托拉西布与多西他赛治疗既往接受过KRAS G12C突变治疗的晚期NSCLC
背景在CodeBreaK 200 III期开放标签试验中,索托拉西布与多西他赛相比,显著提高了既往接受过治疗的KRAS G12C突变晚期非小细胞肺癌(NSCLC)的疗效。与多西他赛相比,索托拉西布在总体健康状况、身体机能、呼吸困难和咳嗽方面的患者报告结果(PROs)更受欢迎。方法在 CodeBreaK 200 中,345 名既往治疗后病情进展的患者接受了索托拉西布(960 毫克,每天口服)或多西他赛(75 毫克/平方米,每 3 周静脉注射一次)治疗。经过验证的问卷调查收集了患者对其生活质量和症状负担的感知,以确定关键的次要和探索性PRO终点,包括欧洲癌症研究和治疗组织生活质量问卷核心30(EORTC QLQ-C30)和生活质量问卷肺癌13(EORTC QLQ-LC13)、癌症治疗功能评估工具通用表(FACT-G GP5)中的 GP5 问题、PRO-不良事件通用术语标准(PRO-CTCAE)和包括视觉模拟量表(EQ-5D VAS)在内的 5 级 EuroQOL-5 维度(EQ-5D-5L)。结果与接受多西他赛治疗的患者相比,接受索托拉西布治疗的患者受到治疗副作用的困扰较少(几率比 [OR] 5.7),而且症状的严重程度较低(疼痛:OR 2.9;肌肉酸痛:OR 2.9):疼痛:OR 2.9;肌肉酸痛OR 4.4;关节疼痛:OR 4.2;口腔或咽喉疼痛:OR 4.3)。此外,患者的症状对日常活动的影响也较小(疼痛:OR 3.2;肌肉酸痛:OR 3.9;关节酸痛:OR 10.7)。索托拉西布治疗后患者的生活质量保持稳定,但多西他赛治疗后患者的生活质量恶化(EQ-5D VAS评分与基线相比的变化:第1周期第5天为1.5 vs -8.4,第12周为2.2 vs -5.8)。与多西他赛相比,索托拉西除了能改善临床疗效外,还能维持患者的生活质量,这表明索托拉西可能是KRAS G12C突变晚期NSCLC患者更容易耐受的治疗选择。
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来源期刊
Lung Cancer
Lung Cancer 医学-呼吸系统
CiteScore
9.40
自引率
3.80%
发文量
407
审稿时长
25 days
期刊介绍: Lung Cancer is an international publication covering the clinical, translational and basic science of malignancies of the lung and chest region.Original research articles, early reports, review articles, editorials and correspondence covering the prevention, epidemiology and etiology, basic biology, pathology, clinical assessment, surgery, chemotherapy, radiotherapy, combined treatment modalities, other treatment modalities and outcomes of lung cancer are welcome.
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