TY - JOUR
T1 - Determinants of anti-PD-1 response and resistance in clear cell renal cell carcinoma
AU - PEACE Consortium
AU - TRACERx Renal Consortium
AU - Au, Lewis
AU - Hatipoglu, Emine
AU - Robert de Massy, Marc
AU - Litchfield, Kevin
AU - Beattie, Gordon
AU - Rowan, Andrew
AU - Schnidrig, Desiree
AU - Thompson, Rachael
AU - Byrne, Fiona
AU - Horswell, Stuart
AU - Fotiadis, Nicos
AU - Hazell, Steve
AU - Nicol, David
AU - Shepherd, Scott T.C.
AU - Fendler, Annika
AU - Mason, Robert
AU - Del Rosario, Lyra
AU - Edmonds, Kim
AU - Lingard, Karla
AU - Sarker, Sarah
AU - Mangwende, Mary
AU - Carlyle, Eleanor
AU - Attig, Jan
AU - Joshi, Kroopa
AU - Uddin, Imran
AU - Becker, Pablo D.
AU - Sunderland, Mariana Werner
AU - Akarca, Ayse
AU - Puccio, Ignazio
AU - Yang, William W.
AU - Lund, Tom
AU - Dhillon, Kim
AU - Vasquez, Marcos Duran
AU - Ghorani, Ehsan
AU - Xu, Hang
AU - Spencer, Charlotte
AU - López, José I.
AU - Green, Anna
AU - Mahadeva, Ula
AU - Borg, Elaine
AU - Mitchison, Miriam
AU - Moore, David A.
AU - Proctor, Ian
AU - Falzon, Mary
AU - Pickering, Lisa
AU - Furness, Andrew J.S.
AU - Reading, James L.
AU - Salgado, Roberto
AU - Marafioti, Teresa
AU - Caldas, Carlos
N1 - Publisher Copyright:
© 2021 The Authors
PY - 2021/11/8
Y1 - 2021/11/8
N2 - 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.
AB - 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.
KW - T cell receptor
KW - TCR clonal maintenance
KW - TCR clonal replacement
KW - anti-PD-1
KW - autopsy
KW - clear cell renal cell carcinoma
KW - human endogenous retrovirus
KW - multiregion
KW - nivolumab
UR - https://www.scopus.com/pages/publications/85119606374
U2 - 10.1016/j.ccell.2021.10.001
DO - 10.1016/j.ccell.2021.10.001
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C2 - 34715028
AN - SCOPUS:85119606374
SN - 1535-6108
VL - 39
SP - 1497-1518.e11
JO - Cancer Cell
JF - Cancer Cell
IS - 11
ER -