Tumour-infiltrating lymphocytes in non-invasive breast cancer: A systematic review and meta-analysis.


Journal

Breast (Edinburgh, Scotland)
ISSN: 1532-3080
Titre abrégé: Breast
Pays: Netherlands
ID NLM: 9213011

Informations de publication

Date de publication:
Oct 2021
Historique:
received: 25 05 2021
revised: 01 07 2021
accepted: 03 07 2021
pubmed: 18 7 2021
medline: 16 10 2021
entrez: 17 7 2021
Statut: ppublish

Résumé

The role of tumour infiltrating lymphocytes (TILs) as a biomarker in non-invasive breast cancer is unclear. This meta-analysis assessed the prognostic impact of TIL levels in patients with non-invasive breast cancer. Systematic literature search was performed to identify studies assessing local recurrence in patients with non-invasive breast cancer according to TIL levels (high vs. low). Subgroup analyses per local recurrence (invasive and non-invasive) were performed. Secondary objectives were the association between TIL levels and non-invasive breast cancer subtypes, age, grade and necrosis. Odds ratios (ORs) and 95% confidence intervals (CI) were extracted from each study and a pooled analysis was conducted with random-effect model. Seven studies (N = 3437) were included in the present meta-analysis. High-TILs were associated with a higher likelihood of local recurrence (invasive or non-invasive, N = 2941; OR 2.05; 95%CI, 1.03-4.08; p = 0.042), although with a lower likelihood of invasive local recurrence (N = 1722; OR 0.69; 95%CI, 0.49-0.99; p = 0.042). High-TIL levels were associated with triple-negative (OR 3.84; 95%CI, 2.23-6.61; p < 0.001) and HER2-positive (OR 6.27; 95%CI, 4.93-7.97; p < 0.001) subtypes, high grade (OR 5.15; 95%CI, 3.69-7.19; p < 0.001) and necrosis (OR 3.09; 95%CI, 2.33-4.10; p < 0.001). High-TIL levels were associated with more aggressive tumours, a higher likelihood of local recurrence (invasive or non-invasive) but a lower likelihood of invasive local recurrence in patients with non-invasive breast cancer.

Sections du résumé

BACKGROUND BACKGROUND
The role of tumour infiltrating lymphocytes (TILs) as a biomarker in non-invasive breast cancer is unclear. This meta-analysis assessed the prognostic impact of TIL levels in patients with non-invasive breast cancer.
METHODS METHODS
Systematic literature search was performed to identify studies assessing local recurrence in patients with non-invasive breast cancer according to TIL levels (high vs. low). Subgroup analyses per local recurrence (invasive and non-invasive) were performed. Secondary objectives were the association between TIL levels and non-invasive breast cancer subtypes, age, grade and necrosis. Odds ratios (ORs) and 95% confidence intervals (CI) were extracted from each study and a pooled analysis was conducted with random-effect model.
RESULTS RESULTS
Seven studies (N = 3437) were included in the present meta-analysis. High-TILs were associated with a higher likelihood of local recurrence (invasive or non-invasive, N = 2941; OR 2.05; 95%CI, 1.03-4.08; p = 0.042), although with a lower likelihood of invasive local recurrence (N = 1722; OR 0.69; 95%CI, 0.49-0.99; p = 0.042). High-TIL levels were associated with triple-negative (OR 3.84; 95%CI, 2.23-6.61; p < 0.001) and HER2-positive (OR 6.27; 95%CI, 4.93-7.97; p < 0.001) subtypes, high grade (OR 5.15; 95%CI, 3.69-7.19; p < 0.001) and necrosis (OR 3.09; 95%CI, 2.33-4.10; p < 0.001).
CONCLUSIONS CONCLUSIONS
High-TIL levels were associated with more aggressive tumours, a higher likelihood of local recurrence (invasive or non-invasive) but a lower likelihood of invasive local recurrence in patients with non-invasive breast cancer.

Identifiants

pubmed: 34273666
pii: S0960-9776(21)00415-X
doi: 10.1016/j.breast.2021.07.007
pmc: PMC8319525
pii:
doi:

Substances chimiques

Receptor, ErbB-2 EC 2.7.10.1

Types de publication

Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

183-192

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest RC received speaker honoraria from Boehringer-Ingelheim, AstraZeneca, and Janssen; and travel grants from Pfizer and AstraZeneca, none related to the present work. EdA has received honoraria from Roche-Genentech, Libbs, Seattle Genetics, Novartis, Pierre Fabre; research grant from Roche-Genentech, Astra Zeneca, GSK/Novartis, Servier (to the institution), and travel grants from Roche-Genentech and GlaxoSmithKline, none related to the present work. All other authors declare no disclosures related to the present work. The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Rafael Caparica (R)

Institut Jules Bordet, Université Libre de Bruxelles (U.L.B.), Brussels, Belgium.

Marco Bruzzone (M)

Clinical Epidemiology Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.

Elisa Agostinetto (E)

Institut Jules Bordet, Université Libre de Bruxelles (U.L.B.), Brussels, Belgium; Humanitas Clinical and Research Center - IRCCS, Humanitas Cancer Center, via Manzoni 56, 20089, Rozzano, Milan, Italy; Humanitas University, Department of Biomedical Sciences, via Rita Levi Montalcini 4, 20090 Pieve Emanuele, Milan, Italy. Electronic address: elisa.agostinetto@bordet.be.

Maria Alice Franzoi (MA)

Institut Jules Bordet, Université Libre de Bruxelles (U.L.B.), Brussels, Belgium.

Marcello Ceppi (M)

Clinical Epidemiology Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.

Nina Radosevic-Robin (N)

INSERM U1240, University Clermont Auvergne, Centre Jean Perrin, Department of Pathology, Clermont-Ferrand, France.

Frédérique Penault-Llorca (F)

INSERM U1240, University Clermont Auvergne, Centre Jean Perrin, Department of Pathology, Clermont-Ferrand, France.

Karen Willard-Gallo (K)

Molecular Immunology Laboratory, Institut Jules Bordet, Brussels, Belgium.

Sherene Loi (S)

Peter MacCallum Cancer Centre, Melbourne, Australia.

Roberto Salgado (R)

Peter MacCallum Cancer Centre, Melbourne, Australia; Department of Pathology, GZA-ZNA, Antwerp, Belgium.

Evandro de Azambuja (E)

Institut Jules Bordet, Université Libre de Bruxelles (U.L.B.), Brussels, Belgium.

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Classifications MeSH