Evolutionary and immune microenvironment dynamics during neoadjuvant treatment of oesophagael adenocarcinoma.


Journal

Research square
Titre abrégé: Res Sq
Pays: United States
ID NLM: 101768035

Informations de publication

Date de publication:
13 Apr 2023
Historique:
pubmed: 24 4 2023
medline: 24 4 2023
entrez: 24 04 2023
Statut: epublish

Résumé

Locally advanced oesophageal adenocarcinoma (EAC) remains difficult to treat because of common resistance to neoadjuvant therapy and high recurrence rates. The ecological and evolutionary dynamics responsible for treatment failure are incompletely understood. Here, we performed a comprehensive multi-omic analysis of samples collected from EAC patients in the MEMORI clinical trial, revealing major changes in gene expression profiles and immune microenvironment composition that did not appear to be driven by changes in clonal composition. Multi-region multi-timepoint whole exome (300x depth) and paired transcriptome sequencing was performed on 27 patients pre-, during and after neoadjuvant treatment. EAC showed major transcriptomic changes during treatment with upregulation of immune and stromal pathways and oncogenic pathways such as KRAS, Hedgehog and WNT. However, genetic data revealed that clonal sweeps were rare, suggesting that gene expression changes were not clonally driven. Additional longitudinal image mass cytometry was performed in a subset of 15 patients and T-cell receptor sequencing in 10 patients, revealing remodelling of the T-cell compartment during treatment and other shifts in microenvironment composition. The presence of immune escape mechanisms and a lack of clonal T-cell expansions were linked to poor clinical treatment response. This study identifies profound transcriptional changes during treatment with limited evidence that clonal replacement is the cause, suggesting phenotypic plasticity and immune dynamics as mechanisms for therapy resistance with pharmacological relevance.

Identifiants

pubmed: 37090678
doi: 10.21203/rs.3.rs-2738048/v1
pmc: PMC10120745
pii:
doi:

Types de publication

Preprint

Langues

eng

Auteurs

Melissa Barroux (M)

Medical Clinic and Polyclinic II, Klinikum rechts der Isar, Technical University of Munich.

Jacob Househam (J)

Institute of Cancer Research.

Eszter Lakatos (E)

Institute of Cancer Research.

Tahel Ronel (T)

Barts Cancer Institute, Queen Mary University of London.

Henrike Salié (H)

University Medical Center Freiburg.

Max Mossner (M)

Institute of Cancer Research.

Kane Smith (K)

Institute of Cancer Research.

Chris Kimberley (C)

Barts Cancer Institute, Queen Mary University of London.

Salpie Nowinski (S)

Institute of Cancer Research.

Alison Berner (A)

Barts Cancer Institute, Queen Mary University of London.

Vinaya Gunasri (V)

Institute of Cancer Research.

Mamix Jansen (M)

UCL Cancer Institute: University College London Cancer Institute.

Giulio Caravagna (G)

University of Trieste.

Katja Steiger (K)

Institute of Pathology, School of Medicine, Technical University of Munich.

Julia Slotta-Huspenina (J)

Institute for Pathology, Technische Universität München.

Wilko Weichert (W)

Technische Universität München.

Markus Alberstmeier (M)

University Hospital, Ludwig-Maximilians-Universität (LMU) Munich.

Helmut Friess (H)

Department of Surgery, Klinikum rechts der Isar, Technical University of Munich.

Bertram Bengsch (B)

University Medical Center Freiburg.

Roland Schmid (R)

Medizinische Klinik und Poliklinik II, Klinikum rechts der Isar, Technische Universität München.

Jens Siveke (J)

German Cancer Consortium (DKTK) partner site Essen and Institute for Developmental Cancer Therapeutics (BIT), University Hospital Essen at the University Duisburg-Essen, Germany.

Trevor Graham (T)

Institute of Cancer Research.

Classifications MeSH