Survival outcomes of metastatic breast cancer patients by germline BRCA1/2 status in a large multicenter real-world database.


Journal

International journal of cancer
ISSN: 1097-0215
Titre abrégé: Int J Cancer
Pays: United States
ID NLM: 0042124

Informations de publication

Date de publication:
01 03 2023
Historique:
revised: 17 07 2022
received: 05 04 2022
accepted: 09 08 2022
pubmed: 27 9 2022
medline: 6 1 2023
entrez: 26 9 2022
Statut: ppublish

Résumé

The outcomes and best treatment strategies for germline BRCA1/2 mutation (gBRCAm) carriers with metastatic breast cancer (MBC) remain uncertain. We compared the overall survival and the first line progression free survival (PFS1) of patients with a gBRCAm identified at initiation of first-line treatment with those of BRCA wild-type (WT) and not-tested (NT) individuals in the ESME real-world database of MBC patients between 2008 and 2016 (NCT03275311). Among the 20 624 eligible patients, 325 had a gBRCAm, 1138 were WT and 19 161 NT. Compared with WT, gBRCAm carriers were younger, and had more aggressive diseases. At a median follow-up of 50.5 months, median OS was 30.6 (95%CI: 21.9-34.3), 35.8 (95%CI: 32.2-37.8) and 39.3 months (95% CI: 38.3-40.3) in the gBRCAm, WT and NT subgroups, respectively. Median PFS1 was 7.9 (95%CI: 6.6-9.3), 7.8 (95%CI: 7.3-8.5) and 9.7 months (95%CI, 9.5-10.0). In the multivariable analysis conducted in the whole cohort, gBRCAm status had however no independent prognostic impact on OS and PFS1. Though, in the triple-negative subgroup, gBRCAm patients had better OS and PFS1 (HR vs WT = 0.76; 95%CI: 0.60-0.97; P = .027 and 0.69; 95% CI: 0.55-0.86; P = .001, respectively). In contrast, in patients with HR+/HER2 negative cancers, PFS1 appeared significantly and OS non significantly lower for gBRCAm carriers (PFS1: HR vs WT = 1.23; 95%CI: 1.03-1.46; P = .024; OS:HR = 1.22, 95% CI: 0.97-1.52, P = .089). In conclusion, gBRCA1/2 status appears to have divergent survival effects in MBC according to IHC subtype.

Identifiants

pubmed: 36161271
doi: 10.1002/ijc.34304
pmc: PMC10092337
doi:

Substances chimiques

BRCA1 Protein 0
BRCA1 protein, human 0
BRCA2 protein, human 0

Banques de données

ClinicalTrials.gov
['NCT03275311']

Types de publication

Multicenter Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

921-931

Informations de copyright

© 2022 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC.

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Auteurs

Audrey Mailliez (A)

Center Oscar Lambret, Lille, France.

Veronique D'Hondt (V)

Institut régional du Cancer Montpellier/Val d'Aurelle, Montpellier, France.

Amelie Lusque (A)

Institut Claudius Regaud, IUCT-Oncopole, Toulouse, France.

Olivier Caron (O)

Institut Gustave Roussy, Villejuif, France.

Luc Cabel (L)

Institut Curie, Paris et Saint Cloud, France.

Anthony Goncalves (A)

Institut Paoli-Calmette, Marseille, France.

Marc Debled (M)

Institut Bergonié, Bordeaux, France.

Laurence Gladieff (L)

Institut Claudius Regaud, IUCT-Oncopole, Toulouse, France.

Jean-Marc Ferrero (JM)

Center Antoine Lacassagne, Nice, France.

Thierry Petit (T)

Center Paul Strauss, Strasbourg, France.

Marie Ange Mouret-Reynier (MA)

Center Jean Perrin, Clermont Ferrand, France.

Jean-Christophe Eymard (JC)

Institut Jean Godinot, Reims, France.

Christelle Levy (C)

Center François Baclesse, Caen, France.

Lionel Uwer (L)

Institut de Cancerologie de Lorraine, Vandoeuvre-lès-Nancy, France.

Marianne Leheurteur (M)

Center Henri Becquerel, Rouen, France.

Isabelle Desmoulins (I)

Center Georges François Leclerc, Dijon, France.

Thomas Bachelot (T)

Center Léon Bérard, Lyon, France.

Jean-Sebastien Frenel (JS)

Institut de cancérologie de l'Ouest, Nantes et Angers, France.

Thibault de la Motte Rouge (T)

Center Eugène Marquis, Rennes, France.

Gaëtane Simon (G)

Unicancer, Paris, France.

William Jacot (W)

Institut régional du Cancer Montpellier/Val d'Aurelle, Montpellier, France.

Suzette Delaloge (S)

Institut Gustave Roussy, Villejuif, France.

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Classifications MeSH