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dc.contributor.authorAu, L
dc.contributor.authorHatipoglu, E
dc.contributor.authorRobert de Massy, M
dc.contributor.authorLitchfield, K
dc.contributor.authorBeattie, G
dc.contributor.authorRowan, A
dc.contributor.authorSchnidrig, D
dc.contributor.authorThompson, R
dc.contributor.authorByrne, F
dc.contributor.authorHorswell, S
dc.contributor.authorFotiadis, N
dc.contributor.authorHazell, S
dc.contributor.authorNicol, D
dc.contributor.authorShepherd, STC
dc.contributor.authorFendler, A
dc.contributor.authorMason, R
dc.contributor.authorDel Rosario, L
dc.contributor.authorEdmonds, K
dc.contributor.authorLingard, K
dc.contributor.authorSarker, S
dc.contributor.authorMangwende, M
dc.contributor.authorCarlyle, E
dc.contributor.authorAttig, J
dc.contributor.authorJoshi, K
dc.contributor.authorUddin, I
dc.contributor.authorBecker, PD
dc.contributor.authorSunderland, MW
dc.contributor.authorAkarca, A
dc.contributor.authorPuccio, I
dc.contributor.authorYang, WW
dc.contributor.authorLund, T
dc.contributor.authorDhillon, K
dc.contributor.authorVasquez, MD
dc.contributor.authorGhorani, E
dc.contributor.authorXu, H
dc.contributor.authorSpencer, C
dc.contributor.authorLópez, JI
dc.contributor.authorGreen, A
dc.contributor.authorMahadeva, U
dc.contributor.authorBorg, E
dc.contributor.authorMitchison, M
dc.contributor.authorMoore, DA
dc.contributor.authorProctor, I
dc.contributor.authorFalzon, M
dc.contributor.authorPickering, L
dc.contributor.authorFurness, AJS
dc.contributor.authorReading, JL
dc.contributor.authorSalgado, R
dc.contributor.authorMarafioti, T
dc.contributor.authorJamal-Hanjani, M
dc.contributor.authorPEACE Consortium,
dc.contributor.authorKassiotis, G
dc.contributor.authorChain, B
dc.contributor.authorLarkin, J
dc.contributor.authorSwanton, C
dc.contributor.authorQuezada, SA
dc.contributor.authorTurajlic, S
dc.contributor.authorTRACERx Renal Consortium,
dc.date.accessioned2022-02-01T16:20:42Z
dc.date.available2022-02-01T16:20:42Z
dc.date.issued2021-11-08
dc.identifier.citationCancer cell, 2021, 39 (11), pp. 1497 - 1518.e11
dc.identifier.issn1535-6108
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/4993
dc.identifier.eissn1878-3686
dc.identifier.eissn1878-3686
dc.identifier.doi10.1016/j.ccell.2021.10.001
dc.identifier.doi10.1016/j.ccell.2021.10.001
dc.description.abstractADAPTeR 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.
dc.formatPrint-Electronic
dc.format.extent1497 - 1518.e11
dc.languageeng
dc.language.isoeng
dc.publisherCELL PRESS
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectPEACE Consortium
dc.subjectTRACERx Renal Consortium
dc.subjectCD8-Positive T-Lymphocytes
dc.subjectHumans
dc.subjectEndogenous Retroviruses
dc.subjectCarcinoma, Renal Cell
dc.subjectKidney Neoplasms
dc.subjectReceptors, Antigen, T-Cell
dc.subjectProspective Studies
dc.subjectGene Expression Profiling
dc.subjectSequence Analysis, RNA
dc.subjectGenomics
dc.subjectTumor Escape
dc.subjectDrug Resistance, Neoplasm
dc.subjectClinical Trials, Phase II as Topic
dc.subjectSingle-Cell Analysis
dc.subjectTumor Microenvironment
dc.subjectWhole Exome Sequencing
dc.subjectNivolumab
dc.subjectImmune Checkpoint Inhibitors
dc.titleDeterminants of anti-PD-1 response and resistance in clear cell renal cell carcinoma.
dc.typeJournal Article
dcterms.dateAccepted2021-10-06
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1016/j.ccell.2021.10.001
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
dc.relation.isPartOfCancer cell
pubs.issue11
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/ImmNet
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.publication-statusPublished
pubs.volume39
pubs.embargo.termsNot known
dc.contributor.icrauthorAu, Lewis
dc.contributor.icrauthorShepherd, Scott
dc.contributor.icrauthorFurness, Andrew


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