Residual cancer burden index and tumor-infiltrating lymphocyte subtypes in triple-negative breast cancer after neoadjuvant chemotherapy.


Journal

Breast cancer research and treatment
ISSN: 1573-7217
Titre abrégé: Breast Cancer Res Treat
Pays: Netherlands
ID NLM: 8111104

Informations de publication

Date de publication:
Jan 2020
Historique:
received: 02 07 2019
accepted: 05 09 2019
pubmed: 19 9 2019
medline: 2 10 2020
entrez: 19 9 2019
Statut: ppublish

Résumé

There is a need to refine the prognosis of triple-negative breast cancer (TNBC) patients after neoadjuvant chemotherapy (NAC) and to study the influence of the tumor microenvironment. We evaluated the prognostic value of pathological and immune markers in TNBC with residual disease (RD) after NAC. In a series of 186 TNBC patients treated by NAC, we assessed the prognostic value of the Residual Cancer Burden (RCB) index. In 109 patients with RD, we studied the impact of clinicopathological features and tumor immune response in the residual tumor on overall survival (OS) and distant recurrence-free interval (DRFI). In the whole group, the OS and DRFI, at 3 years, were statistically different between the different classes of RCB (P = 0.0004 and P < 0.0001, respectively). In univariate analysis of the RD group, low RCB index and high ratios of stromal tumor-infiltrating lymphocytes (TILs), CD3 + TILs, CD4 + TILs, CD8 + TILs, and IDO1-positive cells were significant favorable prognostic factors for DRFI at 3 years. In the final multivariate model, CD4 + TILs and RCB index showed a statistically independent prognostic significance for DRFI [Hazard Ratio (HR) 2.88 (95%CI 1.34-6.17), P = 0.007 and HR 12.04 (95%CI 2.78-52.23, P < 0.0001), respectively]. The CD4 + TIL levels influenced survival in the different RCB classes with a significant effect observed in RCB-II and RCB-III classes (P = 0.05 and P = 0.05, respectively). These results suggest that the combination of pathological (RCB index) and tumor micro-environmental features (CD4 + TILs) help refining the prognosis of TNBC patients with RD following NAC.

Identifiants

pubmed: 31529299
doi: 10.1007/s10549-019-05437-z
pii: 10.1007/s10549-019-05437-z
doi:

Substances chimiques

Antineoplastic Agents 0
Biomarkers 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

11-23

Auteurs

Clémence Pinard (C)

Department of Biopathology, Institut Bergonié, Comprehensive Cancer Center, 229 Cours de l'Argonne CS61283-33076, 33000, Bordeaux, Cedex, France.
University of Bordeaux, 33000, Bordeaux, France.

Marc Debled (M)

Department of Medical Oncology, Institut Bergonié, 33000, Bordeaux, France.

Houda Ben Rejeb (H)

Department of Biopathology, Institut Bergonié, Comprehensive Cancer Center, 229 Cours de l'Argonne CS61283-33076, 33000, Bordeaux, Cedex, France.

Valérie Velasco (V)

Department of Biopathology, Institut Bergonié, Comprehensive Cancer Center, 229 Cours de l'Argonne CS61283-33076, 33000, Bordeaux, Cedex, France.

Christine Tunon de Lara (C)

Department of Surgery, Institut Bergonié, 33000, Bordeaux, France.

Stéphanie Hoppe (S)

Department of Clinical Research and Medical Information, Institut Bergonié, 33000, Bordeaux, France.

Elodie Richard (E)

INSERM U1218, 33000, Bordeaux, France.

Véronique Brouste (V)

Department of Clinical Research and Medical Information, Institut Bergonié, 33000, Bordeaux, France.

Hervé Bonnefoi (H)

University of Bordeaux, 33000, Bordeaux, France.
Department of Medical Oncology, Institut Bergonié, 33000, Bordeaux, France.
INSERM U1218, 33000, Bordeaux, France.

Gaëtan MacGrogan (G)

Department of Biopathology, Institut Bergonié, Comprehensive Cancer Center, 229 Cours de l'Argonne CS61283-33076, 33000, Bordeaux, Cedex, France. G.MacGrogan@bordeaux.unicancer.fr.
INSERM U1218, 33000, Bordeaux, France. G.MacGrogan@bordeaux.unicancer.fr.

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Classifications MeSH