作者
Barzin Y Nabet, Mohammad S Esfahani, Everett J Moding, Emily G Hamilton, Jacob J Chabon, Hira Rizvi, Chloe B Steen, Aadel A Chaudhuri, Chih Long Liu, Angela B Hui, Diego Almanza, Henning Stehr, Linda Gojenola, Rene F Bonilla, Michael C Jin, Young-Jun Jeon, Diane Tseng, Cailian Liu, Taha Merghoub, Joel W Neal, Heather A Wakelee, Sukhmani K Padda, Kavitha J Ramchandran, Millie Das, Andrew J Plodkowski, Christopher Yoo, Emily L Chen, Ryan B Ko, Aaron M Newman, Matthew D Hellmann, Ash A Alizadeh, Maximilian Diehn
发表日期
2020/10/15
期刊
Cell
卷号
183
期号
2
页码范围
363-376. e13
出版商
Elsevier
简介
Although treatment of non-small cell lung cancer (NSCLC) with immune checkpoint inhibitors (ICIs) can produce remarkably durable responses, most patients develop early disease progression. Furthermore, initial response assessment by conventional imaging is often unable to identify which patients will achieve durable clinical benefit (DCB). Here, we demonstrate that pre-treatment circulating tumor DNA (ctDNA) and peripheral CD8 T cell levels are independently associated with DCB. We further show that ctDNA dynamics after a single infusion can aid in identification of patients who will achieve DCB. Integrating these determinants, we developed and validated an entirely noninvasive multiparameter assay (DIREct-On, Durable Immunotherapy Response Estimation by immune profiling and ctDNA-On-treatment) that robustly predicts which patients will achieve DCB with higher accuracy than any individual …
引用总数
20202021202220232024660856639