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索托拉西布治疗经治 G12C 突变型非小细胞肺癌患者的长期疗效和分子相关性:CodeBreaK 100 的 2 年分析。

Long-Term Outcomes and Molecular Correlates of Sotorasib Efficacy in Patients With Pretreated G12C-Mutated Non-Small-Cell Lung Cancer: 2-Year Analysis of CodeBreaK 100.

机构信息

Roswell Park Comprehensive Cancer Center, Buffalo, NY.

Siteman Cancer Center, Washington University School of Medicine, St Louis, MO.

出版信息

J Clin Oncol. 2023 Jun 20;41(18):3311-3317. doi: 10.1200/JCO.22.02524. Epub 2023 Apr 25.

Abstract

JCO In the longest follow-up, to our knowledge, for a KRAS inhibitor, we assessed the long-term efficacy, safety, and biomarkers of sotorasib in patients with G12C-mutated advanced non-small-cell lung cancer (NSCLC) from the CodeBreaK 100 clinical trial (ClinicalTrials.gov identifier: NCT03600883). This multicenter, single-group, open-label phase I/phase II trial enrolled 174 patients with G12C-mutated, locally advanced or metastatic NSCLC after progression on prior therapies. Patients (N = 174) received sotorasib 960 mg once daily with the primary end points for phase I of safety and tolerability and for phase II of objective response rate (ORR). Sotorasib produced an ORR of 41%, median duration of response of 12.3 months, progression-free survival (PFS) of 6.3 months, overall survival (OS) of 12.5 months, and 2-year OS rate of 33%. Long-term clinical benefit (PFS ≥ 12 months) was observed in 40 (23%) patients across PD-L1 expression levels, in a proportion of patients with somatic and/or alterations, and was associated with lower baseline circulating tumor DNA levels. Sotorasib was well tolerated, with few late-onset treatment-related toxicities, none of which led to treatment discontinuation. These results demonstrate the long-term benefit of sotorasib, including in subgroups with poor prognosis.

摘要

在 KRAS 抑制剂的最长随访中,我们评估了 sotorasib 治疗 G12C 突变型晚期非小细胞肺癌(NSCLC)患者的长期疗效、安全性和生物标志物,这是来自 CodeBreaK 100 临床试验(ClinicalTrials.gov 标识符:NCT03600883)的最长随访。这项多中心、单组、开放标签的 I/II 期试验招募了 174 名经前期治疗进展后患有 G12C 突变、局部晚期或转移性 NSCLC 的患者。患者(N=174)每日接受一次 960 mg 的 sotorasib 治疗,I 期的主要终点是安全性和耐受性,II 期的主要终点是客观缓解率(ORR)。Sotorasib 的 ORR 为 41%,中位缓解持续时间为 12.3 个月,无进展生存期(PFS)为 6.3 个月,总生存期(OS)为 12.5 个月,2 年 OS 率为 33%。在 PD-L1 表达水平、一定比例的存在体细胞和/或改变的患者中观察到了长期临床获益(PFS≥12 个月),比例为 40(23%)。Sotorasib 具有良好的耐受性,罕见迟发性治疗相关毒性,无任何毒性导致治疗中断。这些结果表明 sotorasib 具有长期获益,包括在预后不良的亚组中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c51b/10414711/af0f5c97c54f/jco-41-3311-g002.jpg

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