Treatment patterns and outcomes in KRASG12C‐positive advanced NSCLC patients previously treated with immune checkpoint inhibitors: A Canada-wide real-world, multi-center, retrospective cohort study

IF 4.5 2区 医学 Q1 ONCOLOGY Lung Cancer Pub Date : 2024-08-01 DOI:10.1016/j.lungcan.2024.107898
Samir H. Barghout , Luna Jia Zhan , Starvroula Raptis , Faisal Al-Agha , Niki Esfahanian , Aimee Popovacki , Goulnar Kasymjanova , Francis Proulx-Rocray , Sze Wah Samuel Chan , Matthew Richardson , M. Catherine Brown , Devalben Patel , Michelle Liane Dean , Vishal Navani , Erica Moore , Lane Carvery , Elizabeth Yan , Daniel Goldshtein , Jasmine Cleary-Gosine , Amanda JW Gibson , Stephanie Snow
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Abstract

Objectives

KRAS mutations, particularly KRASG12C, are prevalent in non-small cell lung cancer (NSCLC). Immune checkpoint inhibitors (ICIs) have been a frontline treatment, but recently developed KRASG12C-selective inhibitors, such as sotorasib, present new therapeutic options. We conducted a multi-center retrospective cohort study to gain insights into real-world treatment patterns and outcomes in patients with KRASG12C-positive advanced NSCLC receiving systemic therapy post-ICI treatment.

Methods

From the CAnadian CAncers With Rare Molecular Alterations-Basket Real-world Observational Study (CARMA-BROS), a cohort of 102 patients with KRASG12C-positive advanced NSCLC across 9 Canadian centers diagnosed between 2015 and 2021 was analyzed. Clinico-demographic and treatment data were obtained from electronic health records. Survival outcomes were assessed using Kaplan-Meier curves and Cox proportional hazards models.

Results

The patients (median age 66 years; 58 % female; 99 % current/former tobacco exposure; 59 % PD-L1 ≥ 50 %), exhibited heterogeneous treatment patterns post-ICI. Most patients received ICIs as a first-line therapy, with varying subsequent lines including chemotherapy and targeted therapy. In patients receiving systemic therapy post-ICI, median overall survival was 12.6 months, and real-world progression-free survival was 4.7 months. KRASG12C-selective targeted therapy post-ICI (n = 20) showed longer real-world progression-free survival compared to single-agent chemotherapy (aHR = 0.39, p = 0.012).

Conclusion

This study contributes valuable real-world data on KRASG12C-positive advanced NSCLC post-ICI treatment. The absence of a standard treatment sequencing post-ICI underscores the need for further investigation and consensus-building in the evolving landscape of KRASG12C-targeted therapies.

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曾接受免疫检查点抑制剂治疗的 KRASG12C 阳性晚期 NSCLC 患者的治疗模式和疗效:一项全加拿大真实世界、多中心、回顾性队列研究。
目的:KRAS突变,尤其是KRASG12C突变,在非小细胞肺癌(NSCLC)中十分普遍。免疫检查点抑制剂(ICIs)一直是一线治疗药物,但最近开发的 KRASG12C 选择性抑制剂(如 sotorasib)提供了新的治疗选择。我们开展了一项多中心回顾性队列研究,以深入了解KRASG12C阳性晚期NSCLC患者在接受ICI治疗后接受全身治疗的实际治疗模式和结果:从加拿大罕见分子变异晚期NSCLC患者真实世界观察研究(CARMA-BROS)中,分析了2015年至2021年期间在加拿大9个中心确诊的102例KRASG12C阳性晚期NSCLC患者队列。临床人口学和治疗数据来自电子健康记录。采用 Kaplan-Meier 曲线和 Cox 比例危险模型对生存结果进行评估:患者(中位年龄 66 岁;58 % 为女性;99 % 目前/曾经吸烟;59 % PD-L1 ≥ 50 %)在 ICI 后表现出不同的治疗模式。大多数患者接受 ICI 作为一线治疗,随后接受化疗和靶向治疗。在ICI后接受系统治疗的患者中,中位总生存期为12.6个月,实际无进展生存期为4.7个月。与单药化疗(aHR = 0.39,p = 0.012)相比,ICI 后的 KRASG12C 选择性靶向治疗(n = 20)显示出更长的实际无进展生存期:本研究为KRASG12C阳性晚期NSCLC的ICI后治疗提供了宝贵的真实世界数据。ICI后标准治疗排序的缺失凸显了在KRASG12C靶向疗法不断发展的背景下进一步调查和建立共识的必要性。
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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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