一项全球3期随机对照试验:sotorasib与docetaxel在预处理KRAS g12c突变的晚期非小细胞肺癌中的颅内活性

IF 4.4 2区 医学 Q1 ONCOLOGY
Lung Cancer Pub Date : 2025-09-01 Epub Date: 2025-07-29 DOI:10.1016/j.lungcan.2025.108683
Anne-Marie C Dingemans, Konstantinos Syrigos, Lorenzo Livi, Astrid Paulus, Sang-We Kim, Yuanbin Chen, Enriqueta Felip, Frank Griesinger, Kadoaki Ohashi, Gerard Zalcman, Brett G M Hughes, Jens Benn Sørensen, Normand Blais, Carlos G M Ferreira, Colin R Lindsay, Rafal Dziadziuszko, Patrick J Ward, Cynthia Chinedu Obiozor, Yang Wang, Solange Peters
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引用次数: 0

摘要

目的:利用CodeBreaK 200研究的3期数据评估sotorasib在治疗晚期或转移性KRAS g12c突变的非小细胞肺癌(NSCLC)的成人患者中的疗效和安全性。材料和方法:KRAS g12c突变的NSCLC患者在铂基化疗和检查点抑制剂治疗后进展,1:1随机分配到索托拉西布或多西他赛。一项探索性事后分析评估了治疗后稳定脑转移患者的中枢神经系统(CNS)无进展生存期(PFS)和基线时中枢神经系统进展时间。根据神经肿瘤脑转移瘤(RANO-BM)标准的研究修正反应评估,采用盲法独立中心评价评估措施。结果:在随机分配接受sotorasib (n=171)或docetaxel (n=174)治疗的患者中,基线CNS转移分别出现在40例(23%)和29例(17%)患者中。该患者亚组的中位随访时间为20.0个月,与多西他赛相比,sotorasib的中位中枢神经系统PFS更长(9.6个月vs 4.5个月;风险比,0.43 [95% CI, 0.20-0.92];P = 0.02)。在基线治疗的CNS病变≥10 mm的患者中,sotorasib达到CNS肿瘤缩小≥30%的患者比例比多西他赛高两倍(33.3% vs 15.4%)。基线时中枢神经系统病变患者的治疗相关不良事件与总体研究人群一致。结论:这些结果表明,sotorasib的颅内活动补充了sotorasib与多西他赛观察到的总体PFS益处,其安全性结果与一般CodeBreaK 200人群相似。临床试验注册号:NCT04303780。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intracranial activity of sotorasib vs docetaxel in pretreated KRAS G12C-mutated advanced non-small cell lung cancer from a global, phase 3, randomized controlled trial.

Objectives: To assess the efficacy and safety of sotorasib in patients with brain metastases using data from the phase 3 CodeBreaK 200 study, which evaluated sotorasib in adults with pretreated advanced or metastatic KRAS G12C-mutated non-small cell lung cancer (NSCLC).

Materials and methods: Patients with KRAS G12C-mutated NSCLC who progressed after platinum-based chemotherapy and checkpoint inhibitor therapy were randomized 1:1 to sotorasib or docetaxel. An exploratory post-hoc analysis evaluated central nervous system (CNS) progression-free survival (PFS) and time to CNS progression in patients with treated and stable brain metastases at baseline. Measures were assessed by blinded independent central review per study-modified Response Assessment in Neuro-Oncology Brain Metastases (RANO-BM) criteria.

Results: Of the patients randomly assigned to receive sotorasib (n=171) or docetaxel (n=174), baseline CNS metastases were present in 40 (23%) and 29 (17%) patients, respectively. With a median follow-up of 20.0 months for this patient subgroup, median CNS PFS was longer with sotorasib compared with docetaxel (9.6 vs 4.5 months; hazard ratio, 0.43 [95% CI, 0.20-0.92]; P=0.02). Among patients with baseline treated CNS lesions of ≥10 mm, the percentage of patients who achieved CNS tumor shrinkage of ≥30% was two-fold higher with sotorasib than docetaxel (33.3% vs 15.4%). Treatment-related adverse events among patients with CNS lesions at baseline were consistent with those of the overall study population.

Conclusions: These results suggest intracranial activity with sotorasib complements the overall PFS benefit observed with sotorasib vs docetaxel, with safety outcomes similar to those in the general CodeBreaK 200 population.

Clinical trials registration number: NCT04303780.

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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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