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DOI 10.1016/j.ccell.2021.10.001

Медицинская библиотека · Cancer cell · 2021

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

Au Lewis, Hatipoglu Emine, Robert de Massy Marc, Litchfield Kevin, Beattie Gordon, Rowan Andrew, Schnidrig Desiree, Thompson Rachael, Byrne Fiona, Horswell Stuart, Fotiadis Nicos, Hazell Steve, Nicol David, Shepherd Scott T C, Fendler Annika, Mason Robert, Del Rosario Lyra, Edmonds Kim, Lingard Karla, Sarker Sarah, Mangwende Mary, Carlyle Eleanor, Attig Jan, Joshi Kroopa, Uddin Imran, Becker Pablo D, Sunderland Mariana Werner, Akarca Ayse, Puccio Ignazio, Yang William W, Lund Tom, Dhillon Kim, Vasquez Marcos Duran, Ghorani Ehsan, Xu Hang, Spencer Charlotte, López José I, Green Anna, Mahadeva Ula, Borg Elaine, Mitchison Miriam, Moore David A, Proctor Ian, Falzon Mary, Pickering Lisa, Furness Andrew J S, Reading James L, Salgado Roberto, Marafioti Teresa, Jamal-Hanjani Mariam, PEACE Consortium, Kassiotis George, Chain Benny, Larkin James, Swanton Charles, Quezada Sergio A, Turajlic Samra, TRACERx Renal Consortium

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Аннотация

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.

Для цитирования: Au Lewis, Hatipoglu Emine, Robert de Massy Marc, Litchfield Kevin, Beattie Gordon, Rowan Andrew, Schnidrig Desiree, Thompson Rachael, Byrne Fiona, Horswell Stuart, Fotiadis Nicos, Hazell Steve, Nicol David, Shepherd Scott T C, Fendler Annika, Mason Robert, Del Rosario Lyra, Edmonds Kim, Lingard Karla, Sarker Sarah, Mangwende Mary, Carlyle Eleanor, Attig Jan, Joshi Kroopa, Uddin Imran, Becker Pablo D, Sunderland Mariana Werner, Akarca Ayse, Puccio Ignazio, Yang William W, Lund Tom, Dhillon Kim, Vasquez Marcos Duran, Ghorani Ehsan, Xu Hang, Spencer Charlotte, López José I, Green Anna, Mahadeva Ula, Borg Elaine, Mitchison Miriam, Moore David A, Proctor Ian, Falzon Mary, Pickering Lisa, Furness Andrew J S, Reading James L, Salgado Roberto, Marafioti Teresa, Jamal-Hanjani Mariam, PEACE Consortium, Kassiotis George, Chain Benny, Larkin James, Swanton Charles, Quezada Sergio A, Turajlic Samra, TRACERx Renal Consortium. Determinants of anti-PD-1 response and resistance in clear cell renal cell carcinoma.. Cancer cell. 2021. DOI: 10.1016/j.ccell.2021.10.001.

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