
Faculty, Staff and Student Publications
Publication Date
6-1-2024
Journal
MedComm
Abstract
Tumor mutational burden (TMB) and T-cell receptor (TCR) might predict the response to immunotherapy in patients with non-small cell lung cancer (NSCLC). However, the predictive value of the combination of TMB and TCR was not clear. Targeted DNA and TCR sequencing were performed on tumor biopsy specimens. We combined TMB and TCR diversity into a TMB-and-TCR (TMR) score using logistic regression. In total, 38 patients with advanced NSCLC were divided into a discovery set (
Keywords
advanced non–small cell lung cancer, clonality, immunotherapy, T‐cell receptors, tumor mutational burden
DOI
10.1002/mco2.604
PMID
38840771
PMCID
PMC11151154
PubMedCentral® Posted Date
June 2024
PubMedCentral® Full Text Version
Post-print
Published Open-Access
yes
Included in
Bioinformatics Commons, Biomedical Informatics Commons, Medical Sciences Commons, Oncology Commons
Comments
Supplementary Material
Data Availability Statement
PMID: 38840771