化疗
肺癌
癌症研究
循环肿瘤细胞
循环肿瘤DNA
DNA
肿瘤科
医学
生物
癌症
内科学
转移
遗传学
作者
Jiachen Xu,Rui Wan,Yiran Cai,Shangli Cai,Lin Wu,Baolan Li,Jianchun Duan,Ying Cheng,Xiaoling Li,Xicheng Wang,Liang Han,Xiaohong Wu,Yun Fan,Yan Yu,Dongqing Lv,Jianhua Shi,Jianjin Huang,Shaozhang Zhou,Baohui Han,Guogui Sun
出处
期刊:Cancer Cell
[Cell Press]
日期:2024-09-01
卷期号:42 (9): 1598-1613.e4
被引量:2
标识
DOI:10.1016/j.ccell.2024.08.013
摘要
Stratification strategies for chemotherapy plus PD-1 inhibitors in advanced non-small-cell lung cancer (NSCLC) are critically demanded. We performed high-throughput panel-based deep next-generation sequencing and low-pass whole genome sequencing on prospectively collected circulating tumor DNA (ctDNA) specimens from 460 patients in the phase 3 CHOICE-01 study at different time points. We identified predictive markers for chemotherapy plus PD-1 inhibitor, including ctDNA status and genomic features such as blood-based tumor mutational burden, intratumor heterogeneity, and chromosomal instability. Furthermore, we established an integrated ctDNA-based stratification strategy, blood-based genomic immune subtypes (bGIS) scheme, to distinguish patients who benefit from the addition of PD-1 inhibitor to first-line chemotherapy. Moreover, we demonstrated potential applications for the dynamic monitoring of ctDNA. Overall, we proposed a potential therapeutic algorithm based on the ctDNA-based stratification strategy, shedding light on the individualized management of immune-chemotherapies for patients with advanced NSCLC.
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