Tumor-Infiltrating Lymphocytes and Prognosis: A Pooled Individual Patient Analysis of Early-Stage Triple-Negative Breast Cancers.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
01 03 2019
Historique:
pubmed: 17 1 2019
medline: 18 12 2019
entrez: 17 1 2019
Statut: ppublish

Résumé

The aim of the current study was to conduct a pooled analysis of studies that have investigated the prognostic value of tumor-infiltrating lymphocytes (TILs) in early-stage triple negative breast cancer (TNBC). Participating studies had evaluated the percentage infiltration of stromally located TILs (sTILs) that were quantified in the same manner in patient diagnostic samples of early-stage TNBC treated with anthracycline-based chemotherapy with or without taxanes. Cox proportional hazards regression models stratified by trial were used for invasive disease-free survival (iDFS; primary end point), distant disease-free survival (D-DFS), and overall survival (OS), fitting sTILs as a continuous variable adjusted for clinicopathologic factors. We collected individual data from 2,148 patients from nine studies. Average age was 50 years (range, 22 to 85 years), and 33% of patients were node negative. The average value of sTILs was 23% (standard deviation, 20%), and 77% of patients had 1% or more sTILs. sTILs were significantly lower with older age ( P = .001), larger tumor size ( P = .01), more nodal involvement ( P = .02), and lower histologic grade ( P = .001). A total of 736 iDFS and 548 D-DFS events and 533 deaths were observed. In the multivariable model, sTILs added significant independent prognostic information for all end points (likelihood ratio χ This pooled data analysis confirms the strong prognostic role of sTILs in early-stage TNBC and excellent survival of patients with high sTILs after adjuvant chemotherapy and supports the integration of sTILs in a clinicopathologic prognostic model for patients with TNBC. This model can be found at www.tilsinbreastcancer.org .

Identifiants

pubmed: 30650045
doi: 10.1200/JCO.18.01010
pmc: PMC7010425
doi:

Substances chimiques

Anthracyclines 0
Taxoids 0

Types de publication

Comparative Study Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

559-569

Subventions

Organisme : NCI NIH HHS
ID : U24 CA075362
Pays : United States

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Auteurs

Sherene Loi (S)

1 Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, VIC, Australia.

Damien Drubay (D)

2 Gustave Roussy, Université Paris-Saclay, Villejuif, France.
3 Université Paris-Sud, Institut National de la Santé et de la Recherche Médicale, Villejuif, France.

Sylvia Adams (S)

4 New York University School of Medicine, New York, NY.

Giancarlo Pruneri (G)

5 Fondazione Istituto di Ricovero e Cura a Carattere Scientifico-Isituto Nazionale dei Tumori, Universita degli Studi di Milano, Milan, Italy.

Prudence A Francis (PA)

1 Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, VIC, Australia.

Magali Lacroix-Triki (M)

2 Gustave Roussy, Université Paris-Saclay, Villejuif, France.

Heikki Joensuu (H)

7 Helsinki University Central Hospital, Helsinki, Finland.

Maria Vittoria Dieci (MV)

8 University of Padova, Padova, Italy.
9 Veneto Insitute of Oncology-IOV-IRCCS, Padua, Italy.

Sunil Badve (S)

10 Indiana University, Indianapolis, IN.

Sandra Demaria (S)

11 Weill-Cornell Medicine, New York, NY.

Robert Gray (R)

12 Dana-Farber Cancer Institute, Boston, MA.

Elisabetta Munzone (E)

13 European institute of Oncology, Milan, Italy.

Jerome Lemonnier (J)

6 R&D UNICANCER, Paris, France.

Christos Sotiriou (C)

14 Institut Jules Bordet, Universite Libre de Bruxelles, Brussels, Belgium.

Martine J Piccart (MJ)

14 Institut Jules Bordet, Universite Libre de Bruxelles, Brussels, Belgium.

Pirkko-Liisa Kellokumpu-Lehtinen (PL)

15 Tampere University Hospital, Tampere, Finland.

Andrea Vingiani (A)

16 University of Milan, Milan, Italy.

Kathryn Gray (K)

12 Dana-Farber Cancer Institute, Boston, MA.

Fabrice Andre (F)

2 Gustave Roussy, Université Paris-Saclay, Villejuif, France.
3 Université Paris-Sud, Institut National de la Santé et de la Recherche Médicale, Villejuif, France.

Carsten Denkert (C)

17 Charite Universite Hospital, Berlin, Germany.

Roberto Salgado (R)

1 Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, VIC, Australia.
18 GZA, Antwerp, Belgium.

Stefan Michiels (S)

2 Gustave Roussy, Université Paris-Saclay, Villejuif, France.
3 Université Paris-Sud, Institut National de la Santé et de la Recherche Médicale, Villejuif, France.

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