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
{"title":"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。","authors":"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","doi":"10.1016/j.lungcan.2024.107898","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><p><em>KRAS</em> mutations, particularly <em>KRAS<sup>G12C</sup></em>, are prevalent in non-small cell lung cancer (NSCLC). Immune checkpoint inhibitors (ICIs) have been a frontline treatment, but recently developed KRAS<sup>G12C</sup>-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 <em>KRAS<sup>G12C</sup></em>-positive advanced NSCLC receiving systemic therapy post-ICI treatment.</p></div><div><h3>Methods</h3><p>From the CAnadian CAncers With Rare Molecular Alterations-Basket Real-world Observational Study (CARMA-BROS), a cohort of 102 patients with <em>KRAS<sup>G12C</sup></em>-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.</p></div><div><h3>Results</h3><p>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. KRAS<sup>G12C</sup>-selective targeted therapy post-ICI (n = 20) showed longer real-world progression-free survival compared to single-agent chemotherapy (aHR = 0.39, <em>p</em> = 0.012).</p></div><div><h3>Conclusion</h3><p>This study contributes valuable real-world data on <em>KRAS<sup>G12C</sup></em>-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 KRAS<sup>G12C</sup>-targeted therapies.</p></div>","PeriodicalId":18129,"journal":{"name":"Lung Cancer","volume":"194 ","pages":"Article 107898"},"PeriodicalIF":4.5000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"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\",\"authors\":\"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\",\"doi\":\"10.1016/j.lungcan.2024.107898\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objectives</h3><p><em>KRAS</em> mutations, particularly <em>KRAS<sup>G12C</sup></em>, are prevalent in non-small cell lung cancer (NSCLC). Immune checkpoint inhibitors (ICIs) have been a frontline treatment, but recently developed KRAS<sup>G12C</sup>-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 <em>KRAS<sup>G12C</sup></em>-positive advanced NSCLC receiving systemic therapy post-ICI treatment.</p></div><div><h3>Methods</h3><p>From the CAnadian CAncers With Rare Molecular Alterations-Basket Real-world Observational Study (CARMA-BROS), a cohort of 102 patients with <em>KRAS<sup>G12C</sup></em>-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.</p></div><div><h3>Results</h3><p>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. KRAS<sup>G12C</sup>-selective targeted therapy post-ICI (n = 20) showed longer real-world progression-free survival compared to single-agent chemotherapy (aHR = 0.39, <em>p</em> = 0.012).</p></div><div><h3>Conclusion</h3><p>This study contributes valuable real-world data on <em>KRAS<sup>G12C</sup></em>-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 KRAS<sup>G12C</sup>-targeted therapies.</p></div>\",\"PeriodicalId\":18129,\"journal\":{\"name\":\"Lung Cancer\",\"volume\":\"194 \",\"pages\":\"Article 107898\"},\"PeriodicalIF\":4.5000,\"publicationDate\":\"2024-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Lung Cancer\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S016950022400432X\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Lung Cancer","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S016950022400432X","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
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
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.
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.