Tumor monocyte content predicts immunochemotherapy outcomes in esophageal adenocarcinoma.

cell type deconvolution esophageal cancer immune checkpoint inhibitors immune priming immunochemotherapy molecular profiling predictive biomarkers single-cell RNA-sequencing atlas tumor associated monocytes tumor mutational burden

Journal

Cancer cell
ISSN: 1878-3686
Titre abrégé: Cancer Cell
Pays: United States
ID NLM: 101130617

Informations de publication

Date de publication:
10 07 2023
Historique:
received: 02 08 2022
revised: 07 04 2023
accepted: 14 06 2023
medline: 13 7 2023
pubmed: 12 7 2023
entrez: 11 7 2023
Statut: ppublish

Résumé

For inoperable esophageal adenocarcinoma (EAC), identifying patients likely to benefit from recently approved immunochemotherapy (ICI+CTX) treatments remains a key challenge. We address this using a uniquely designed window-of-opportunity trial (LUD2015-005), in which 35 inoperable EAC patients received first-line immune checkpoint inhibitors for four weeks (ICI-4W), followed by ICI+CTX. Comprehensive biomarker profiling, including generation of a 65,000-cell single-cell RNA-sequencing atlas of esophageal cancer, as well as multi-timepoint transcriptomic profiling of EAC during ICI-4W, reveals a novel T cell inflammation signature (INCITE) whose upregulation correlates with ICI-induced tumor shrinkage. Deconvolution of pre-treatment gastro-esophageal cancer transcriptomes using our single-cell atlas identifies high tumor monocyte content (TMC) as an unexpected ICI+CTX-specific predictor of greater overall survival (OS) in LUD2015-005 patients and of ICI response in prevalent gastric cancer subtypes from independent cohorts. Tumor mutational burden is an additional independent and additive predictor of LUD2015-005 OS. TMC can improve patient selection for emerging ICI+CTX therapies in gastro-esophageal cancer.

Identifiants

pubmed: 37433281
pii: S1535-6108(23)00216-7
doi: 10.1016/j.ccell.2023.06.006
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1222-1241.e7

Subventions

Organisme : Medical Research Council
ID : G0501068
Pays : United Kingdom
Organisme : Cancer Research UK
ID : A21998
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C30423/A2541
Pays : United Kingdom
Organisme : Department of Health
Pays : United Kingdom

Investigateurs

David Ahern (D)
Bob Amess (B)
Kristen Aufiero Ramirez (KA)
Georgina Berridge (G)
Thomas M Carroll (TM)
Joseph A Chadwick (JA)
Jaeho Chang (J)
Jingfei Cheng (J)
Sam T Dobbie (ST)
Magdalena Drozdz (M)
Roman Fischer (R)
Anna Frangou (A)
Hannah S Fuchs (HS)
Lucinda Griffiths (L)
Masato Inoue (M)
Brittany-Amber Jacobs (BA)
Sabrina A James (SA)
Joseph Kaplinsky (J)
Ioannis Karydis (I)
Benedikt M Kessler (BM)
Simon R Lord (SR)
Hantao Lou (H)
Xin Lu (X)
Mary J Macri (MJ)
Katy J McCann (KJ)
Naomi McGregor (N)
Mark R Middleton (MR)
Stewart Norris-Bulpitt (S)
Ayo O Omiyale (AO)
Richard P Owen (RP)
Iliana Peneva (I)
Chansavath Phetsouphanh (C)
Margarida Rei (M)
Toni Ricciardi (T)
Andrew Roth (A)
Carlos Ruiz Puig (CR)
Aileen Ryan (A)
Benjamin Schuster-Böckler (B)
Paulina Siejka-Zielińska (P)
Chunxiao Song (C)
Marketa Tomkova (M)
Benoit J Van den Eynde (BJ)
Gergana Velikova (G)
Ralph R Venhaus (RR)
Michael J White (MJ)
Phil F Xie (PF)

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests S.L.: consulting fees, honoraria, travel/accommodation or research funding (Sanofi, GLG Consulting, Rejuversen, Eisai, Prosigna, Roche, Pfizer, Novartis, Shionogi, Synthon, CRUK, Boehringer Ingelheim, Piqur Therapeutics, AstraZeneca, Carrick Therapeutics, Merck KGaA) and previous employment by Pfizer. A.R.: stock ownership (Amgen, Immunogen). I.K: honoraria, travel/accommodation (BMS , Delcath Inc, Immunocore, Pierre Fabre, Genentech, Merck Serono, Takeda Pharmaceuticals Int.). B.J.V.D.E.: consulting and ownership interests (iTeos Therapeutics, Oncorus, Amgen, Vaccitech). M.R.M.: grants or personal fees (AstraZeneca, Roche, G.S.K., Novartis, Immunocore, BMS, Pfizer, Merck/MSD, Regeneron, BiolineRx, Replimune, Kineta, Silicon Therapeutics and GRAIL). T.M.C.: founder, employee, and shareholder (Cleancard). X.L.: consulting (SimCell). A provisional patent related to applications of the INCITE signature has been filed. No other authors declare competing interests.

Auteurs

Thomas M Carroll (TM)

Ludwig Institute for Cancer Research, University of Oxford, Oxford, UK.

Joseph A Chadwick (JA)

Ludwig Institute for Cancer Research, University of Oxford, Oxford, UK.

Richard P Owen (RP)

Ludwig Institute for Cancer Research, University of Oxford, Oxford, UK.

Michael J White (MJ)

Ludwig Institute for Cancer Research, University of Oxford, Oxford, UK.

Joseph Kaplinsky (J)

Ludwig Institute for Cancer Research, University of Oxford, Oxford, UK.

Iliana Peneva (I)

Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK; NIHR Oxford Biomedical Research Centre, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK.

Anna Frangou (A)

Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK; Big Data Institute, University of Oxford, Oxford, UK.

Phil F Xie (PF)

Ludwig Institute for Cancer Research, University of Oxford, Oxford, UK.

Jaeho Chang (J)

Ludwig Institute for Cancer Research, University of Oxford, Oxford, UK.

Andrew Roth (A)

Department of Pathology and Molecular Medicine, University of British Columbia, Vancouver, Canada; Department of Computer Science, University of British Columbia, Vancouver, Canada; Department of Molecular Oncology, BC Cancer, Vancouver, Canada.

Bob Amess (B)

Ludwig Institute for Cancer Research, University of Oxford, Oxford, UK.

Sabrina A James (SA)

Ludwig Institute for Cancer Research, University of Oxford, Oxford, UK.

Margarida Rei (M)

Ludwig Institute for Cancer Research, University of Oxford, Oxford, UK.

Hannah S Fuchs (HS)

Ludwig Institute for Cancer Research, University of Oxford, Oxford, UK.

Katy J McCann (KJ)

Cancer Research UK Southampton Experimental Cancer Medicine Centre, Cancer Sciences Unit, Faculty of Medicine, University of Southampton, Southampton, UK.

Ayo O Omiyale (AO)

Ludwig Institute for Cancer Research, University of Oxford, Oxford, UK.

Brittany-Amber Jacobs (BA)

Ludwig Institute for Cancer Research, University of Oxford, Oxford, UK.

Simon R Lord (SR)

Department of Oncology, University of Oxford, Oxford, UK.

Stewart Norris-Bulpitt (S)

Early Phase Clinical Trials Unit, Cancer & Haematology Centre, Churchill Hospital, Oxford, UK.

Sam T Dobbie (ST)

Oncology Clinical Trials Office (OCTO), Department of Oncology, University of Oxford, Oxford, UK.

Lucinda Griffiths (L)

Oncology Clinical Trials Office (OCTO), Department of Oncology, University of Oxford, Oxford, UK.

Kristen Aufiero Ramirez (KA)

Ludwig Cancer Research, New York, NY, USA.

Toni Ricciardi (T)

Ludwig Cancer Research, New York, NY, USA.

Mary J Macri (MJ)

Ludwig Cancer Research, New York, NY, USA.

Aileen Ryan (A)

Ludwig Cancer Research, New York, NY, USA.

Ralph R Venhaus (RR)

Ludwig Cancer Research, New York, NY, USA.

Benoit J Van den Eynde (BJ)

Ludwig Institute for Cancer Research, University of Oxford, Oxford, UK; Ludwig Institute for Cancer Research, Brussels, Belgium; de Duve Institute, Université Catholique de Louvain, Brussels, Belgium.

Ioannis Karydis (I)

Cancer Sciences Unit, University of Southampton and Cancer Care Group, University Hospital Southampton NHS Foundation Trust, Southampton, UK.

Benjamin Schuster-Böckler (B)

Ludwig Institute for Cancer Research, University of Oxford, Oxford, UK.

Mark R Middleton (MR)

NIHR Oxford Biomedical Research Centre, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK; Department of Oncology, University of Oxford, Oxford, UK; Early Phase Clinical Trials Unit, Cancer & Haematology Centre, Churchill Hospital, Oxford, UK. Electronic address: mark.middleton@oncology.ox.ac.uk.

Xin Lu (X)

Ludwig Institute for Cancer Research, University of Oxford, Oxford, UK; NIHR Oxford Biomedical Research Centre, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK. Electronic address: xin.lu@ludwig.ox.ac.uk.

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