西妥昔单抗
医学
克拉斯
结直肠癌
内科学
临床终点
肿瘤科
中止
癌症
不利影响
置信区间
原发性肿瘤
胃肠病学
转移
随机对照试验
作者
Rona Yaeger,Nataliya V. Uboha,Meredith S. Pelster,Tanios Bekaii‐Saab,Minal Barve,Joel Saltzman,Joshua K. Sabari,Julio A. Peguero,Andrew Scott Paulson,Pasi A. Jänne,Marcia Cruz‐Correa,Kenna Anderes,Karen Velastegui,Xiaohong Yan,Hirak Der‐Torossian,Samuel J. Klempner,Scott Kopetz
出处
期刊:Cancer Discovery
[American Association for Cancer Research]
日期:2024-04-08
卷期号:14 (6): 982-993
被引量:17
标识
DOI:10.1158/2159-8290.cd-24-0217
摘要
Adagrasib, an irreversible, selective KRASG12C inhibitor, may be an effective treatment in KRASG12C-mutated colorectal cancer, particularly when combined with an anti-EGFR antibody. In this analysis of the KRYSTAL-1 trial, patients with previously treated KRASG12C-mutated unresectable or metastatic colorectal cancer received adagrasib (600 mg twice daily) plus cetuximab. The primary endpoint was objective response rate (ORR) by blinded independent central review. Ninety-four patients received adagrasib plus cetuximab. With a median follow-up of 11.9 months, ORR was 34.0%, disease control rate was 85.1%, and median duration of response was 5.8 months (95% confidence interval [CI], 4.2-7.6). Median progression-free survival was 6.9 months (95% CI, 5.7-7.4) and median overall survival was 15.9 months (95% CI, 11.8-18.8). Treatment-related adverse events (TRAEs) occurred in all patients; grade 3-4 in 27.7% and no grade 5. No TRAEs led to adagrasib discontinuation. Exploratory analyses suggest circulating tumor DNA may identify features of response and acquired resistance.
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