Repository logo
 

Determinants of anti-PD-1 response and resistance in clear cell renal cell carcinoma.

Published version
Peer-reviewed

Type

Article

Change log

Authors

Au, Lewis 
Hatipoglu, Emine 
Robert de Massy, Marc 
Litchfield, Kevin 
Beattie, Gordon 

Abstract

ADAPTeR is a prospective, phase II study of nivolumab (anti-PD-1) in 15 treatment-naive patients (115 multiregion tumor samples) with metastatic clear cell renal cell carcinoma (ccRCC) aiming to understand the mechanism underpinning therapeutic response. Genomic analyses show no correlation between tumor molecular features and response, whereas ccRCC-specific human endogenous retrovirus expression indirectly correlates with clinical response. T cell receptor (TCR) analysis reveals a significantly higher number of expanded TCR clones pre-treatment in responders suggesting pre-existing immunity. Maintenance of highly similar clusters of TCRs post-treatment predict response, suggesting ongoing antigen engagement and survival of families of T cells likely recognizing the same antigens. In responders, nivolumab-bound CD8+ T cells are expanded and express GZMK/B. Our data suggest nivolumab drives both maintenance and replacement of previously expanded T cell clones, but only maintenance correlates with response. We hypothesize that maintenance and boosting of a pre-existing response is a key element of anti-PD-1 mode of action.

Description

Keywords

T cell receptor, TCR clonal maintenance, TCR clonal replacement, anti-PD-1, autopsy, clear cell renal cell carcinoma, human endogenous retrovirus, multiregion, nivolumab, CD8-Positive T-Lymphocytes, Carcinoma, Renal Cell, Clinical Trials, Phase II as Topic, Drug Resistance, Neoplasm, Endogenous Retroviruses, Gene Expression Profiling, Genomics, Humans, Immune Checkpoint Inhibitors, Kidney Neoplasms, Nivolumab, Prospective Studies, Receptors, Antigen, T-Cell, Sequence Analysis, RNA, Single-Cell Analysis, Tumor Escape, Tumor Microenvironment, Exome Sequencing

Journal Title

Cancer Cell

Conference Name

Journal ISSN

1535-6108
1878-3686

Volume Title

39

Publisher

Elsevier BV