克拉斯
医学
内科学
肺癌
数字聚合酶链反应
癌症
肿瘤科
临床试验
循环肿瘤DNA
队列
胃肠病学
结直肠癌
生物
聚合酶链反应
生物化学
基因
作者
Cloud P. Paweletz,Grace A. Heavey,Yanan Kuang,Emily Durlacher,Thian Kheoh,Richard C. Chao,Alexander I. Spira,Konstantinos Leventakos,Melissa L. Johnson,Sai‐Hong Ignatius Ou,Gregory J. Riely,Kenna Anderes,Wenjing Yang,James G. Christensen,Pasi A. Jänne
标识
DOI:10.1158/1078-0432.ccr-23-0795
摘要
Abstract Purpose: Non-invasive monitoring of circulating tumor DNA (ctDNA) has the potential to be a readily available measure for early prediction of clinical response. Here, we report on early ctDNA changes of KRAS G12C in a Phase 2 trial of adagrasib in patients with advanced, KRAS G12C-mutant lung cancer. Experimental Design: We performed serial droplet digital PCR (ddPCR) and plasma NGS on 60 KRAS G12C-mutant patients with lung cancer that participated in cohort A of the KRYSTAL-1 clinical trial. We analyzed the change in ctDNA at 2 specific intervals: Between cycles 1 and 2 and at cycle 4. Changes in ctDNA were compared with clinical and radiographic response. Results: We found that, in general, a maximal response in KRAS G12C ctDNA levels could be observed during the initial approximately 3-week treatment period, well before the first scan at approximately 6 weeks. 35 patients (89.7%) exhibited a decrease in KRAS G12C cfDNA >90% and 33 patients (84.6%) achieved complete clearance by cycle 2. Patients with complete ctDNA clearance at cycle 2 showed an improved objective response rate (ORR) compared with patients with incomplete ctDNA clearance (60.6% vs. 33.3%). Furthermore, complete ctDNA clearance at cycle 4 was associated with an improved overall survival (14.7 vs. 5.4 months) and progression-free survival (HR, 0.3). Conclusions: These results support using early plasma response of KRAS G12C assessed at approximately 3 weeks to anticipate the likelihood of a favorable objective clinical response.
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