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
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.e7Subventions
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.