| Literature DB >> 35543554 |
Jia-Tao Zhang1, Si-Yang Liu1, Wei Gao2, Si-Yang Maggie Liu3,4, Hong-Hong Yan1, Liyan Ji2, Yu Chen1, Yuhua Gong2, Hong-Lian Lu1, Jun-Tao Lin1, Kai Yin1, Ben-Yuan Jiang1, Qiang Nie1, Ri-Qiang Liao1, Song Dong1, Yanfang Guan2, Pingping Dai2, Xu-Chao Zhang1, Jin-Ji Yang1, Hai-Yan Tu1, Xuefeng Xia2, Xin Yi2, Qing Zhou1, Wen-Zhao Zhong1, Xue-Ning Yang1, Yi-Long Wu1.
Abstract
The efficacy and potential limitations of molecular residual disease (MRD) detection urgently need to be fully elucidated in a larger population of non-small cell lung cancer (NSCLC). We enrolled 261 patients with stages I to III NSCLC who underwent definitive surgery, and 913 peripheral blood samples were successfully detected by MRD assay. Within the population, only six patients (3.2%) with longitudinal undetectable MRD recurred, resulting in a negative predictive value of 96.8%. Longitudinal undetectable MRD may define the patients who were cured. The peak risk of developing detectable MRD was approximately 18 months after landmark detection. Correspondingly, the positive predictive value of longitudinal detectable MRD was 89.1%, with a median lead time of 3.4 months. However, brain-only recurrence was less commonly detected by MRD (n = 1/5, 20%). Further subgroup analyses revealed that patients with undetectable MRD might not benefit from adjuvant therapy. Together, these results expound the value of MRD in NSCLC. SIGNIFICANCE: This study confirms the prognostic value of MRD detection in patients with NSCLC after definitive surgery, especially in those with longitudinal undetectable MRD, which might represent the potentially cured population regardless of stage and adjuvant therapy. Moreover, the risk of developing detectable MRD decreased stepwise after 18 months since landmark detection. This article is highlighted in the In This Issue feature, p. 1599. ©2022 The Authors; Published by the American Association for Cancer Research.Entities:
Mesh:
Year: 2022 PMID: 35543554 DOI: 10.1158/2159-8290.CD-21-1486
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 38.272