Spatial architecture of tumour-infiltrating lymphocytes as a prognostic parameter in resected non-small-cell lung cancer.


Journal

European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery
ISSN: 1873-734X
Titre abrégé: Eur J Cardiothorac Surg
Pays: Germany
ID NLM: 8804069

Informations de publication

Date de publication:
01 09 2020
Historique:
received: 27 08 2019
revised: 14 02 2020
accepted: 21 02 2020
pubmed: 9 4 2020
medline: 22 6 2021
entrez: 9 4 2020
Statut: ppublish

Résumé

Tumour-infiltrating lymphocytes (TILs) are critically implicated in the clinical outcome and response to immunotherapy in non-small-cell lung cancer (NSCLC) patients. The functional competence of lymphocyte subpopulations is strongly conditioned by their spatial arrangement within the tumour immune microenvironment. The aim of this study was to determine whether the tissue localization of specific TIL subpopulations might have an impact on the risk of recurrence in surgically resected NSCLC. High-speed scanning of whole slide images was performed on immunohistochemically stained tissue sections from 97 NSCLC patients to assess the number and ratio of CD3+, CD8+ and PD-1+ T-lymphocytes. TIL distribution was computed considering the intratumoural (proximal or distal) and peripheral (invasive margin) localization as well as their location within the fibrotic tissue (immune excluded). The tumour proliferative index was assessed by Ki67 labelling. The impact of TILs number and distribution on clinical-pathological characteristics and outcomes were statistically analysed. High density and percentage of proximal CD8+ TILs and low PD-1-to-CD8 ratio had a positive impact on disease-free-survival (P = 0.03) and overall survival (P = 0.003). An inverse correlation was observed between the abundance of intratumoural CD8+ TILs carrying PD-1 inhibitory receptor and cancer cell proliferation. Cases with high compared to low fraction of immune excluded CD8+ TILs had significantly reduced 5-year overall survival (n events: 22 vs 12; P = 0.04) and disease-free survival (n events: 24 vs 16; P = 0.03) rates while the amount of CD3+ and CD8+ TILs located at the invasive margin had a favourable effect on the clinical course. Mapping TIL subpopulations may implement the definition of prognostic parameters in surgically resected NSCLC.

Identifiants

pubmed: 32267920
pii: 5817917
doi: 10.1093/ejcts/ezaa098
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

619-628

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery. All rights reserved.

Auteurs

Giovanni Bocchialini (G)

Thoracic Surgery, Department of Medicine and Surgery, University Hospital of Parma, Parma, Italy.

Costanza Lagrasta (C)

Department of Medicine and Surgery, Pathology Unit, University Hospital of Parma, Parma, Italy.

Denise Madeddu (D)

Department of Medicine and Surgery, Pathology Unit, University Hospital of Parma, Parma, Italy.

Giulia Mazzaschi (G)

Medical Oncology Unit, Department of Medicine and Surgery, University Hospital of Parma, Parma, Italy.

Davide Marturano (D)

Department of Medicine and Surgery, Pathology Unit, University Hospital of Parma, Parma, Italy.

Francesco Sogni (F)

Department of Medicine and Surgery, Pathology Unit, University Hospital of Parma, Parma, Italy.

Enrico Maria Silini (EM)

Department of Medicine and Surgery, Pathology Unit, University Hospital of Parma, Parma, Italy.

Letizia Gnetti (L)

Department of Medicine and Surgery, Pathology Unit, University Hospital of Parma, Parma, Italy.

Gabriella Becchi (G)

Department of Medicine and Surgery, Pathology Unit, University Hospital of Parma, Parma, Italy.

Michele Rusca (M)

Thoracic Surgery, Department of Medicine and Surgery, University Hospital of Parma, Parma, Italy.

Paolo Carbognani (P)

Thoracic Surgery, Department of Medicine and Surgery, University Hospital of Parma, Parma, Italy.

Luigi Ventura (L)

Thoracic Surgery, Department of Medicine and Surgery, University Hospital of Parma, Parma, Italy.

Cesare Braggio (C)

Thoracic Surgery, Department of Medicine and Surgery, University Hospital of Parma, Parma, Italy.

Marcello Tiseo (M)

Medical Oncology Unit, Department of Medicine and Surgery, University Hospital of Parma, Parma, Italy.

Federico Quaini (F)

Haematology and Bone Marrow Transplantation, Department of Medicine and Surgery, University Hospital of Parma, Parma, Italy.

Luca Ampollini (L)

Thoracic Surgery, Department of Medicine and Surgery, University Hospital of Parma, Parma, Italy.

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