Ontology highlight
ABSTRACT: Purpose
Pancreatic ductal adenocarcinoma (PDAC) trials have evaluated CTLA-4 and/or PD-(L)1 blockade in patients with advanced disease in which bulky tumor burden and limited time to develop antitumor T cells may have contributed to poor clinical efficacy. Here, we evaluated peripheral blood and tumor T cells from patients with PDAC receiving neoadjuvant chemoradiation plus anti-PD-1 (pembrolizumab) versus chemoradiation alone. We analyzed whether PD-1 blockade successfully reactivated T cells in the blood and/or tumor to determine whether lack of clinical benefit could be explained by lack of reactivated T cells versus other factors.Experimental design
We used single-cell transcriptional profiling and TCR clonotype tracking to identify TCR clonotypes from blood that match
SUBMITTER: Ali LR
PROVIDER: S-EPMC10831338 | biostudies-literature | 2024 Feb
REPOSITORIES: biostudies-literature