Outcomes of patients with HER2-negative metastatic breast cancer after platinum- and non-platinum-based first-line chemotherapy among patients with and without pathogenic germline BRCA1/2 mutations.


Journal

British journal of cancer
ISSN: 1532-1827
Titre abrégé: Br J Cancer
Pays: England
ID NLM: 0370635

Informations de publication

Date de publication:
11 2022
Historique:
received: 04 03 2022
accepted: 26 09 2022
revised: 13 09 2022
pubmed: 8 10 2022
medline: 25 11 2022
entrez: 7 10 2022
Statut: ppublish

Résumé

The efficacy and added benefit of platinum-based chemotherapy (PtCT) for metastatic breast cancer (MBC) remain unclear in patients with and without germline BRCA1 or BRCA2 mutations (gBRCA1/2m and gBRCA1/2wt, respectively). We selected from the French national real-world multicentre ESME cohort (2008-2016) all patients with HER2-negative MBC with known gBRCA1/2 status at first-line chemotherapy initiation. Using multivariable Cox models, we compared the outcome (progression-free (PFS) and overall survival (OS)) of first-line PtCT and non-PtCT regimens based on the patients' gBRCA1/2 status and tumour subtype. Patients who received PtCT had more aggressive tumour features. In the multivariable analysis, first-line PtCT was associated with better adjusted PFS and OS in gBRCA1/2m carriers (N = 300), compared with non-PtCT (HR 0.54, 95% CI 0.4-0.73, P < 0.001, and HR 0.70, 95% CI 0.49-0.99, P = 0.047, respectively). Conversely, outcomes were similar in gBRCA1/2wt patients (N = 922) treated with PtCT and non-PtCT, whatever the tumour subtype. Landmark analyses at months 3 and 6 post treatment initiation supported these results. In this pre-PARP inhibitor real-world cohort, PFS and OS were better after PtCT than non-PtCT in patients with gBRCA1/2m, but not in those with gBRCA1/2wt. These results emphasise the need of early gBRCA1/2 testing in patients with MBC. NCT03275311.

Sections du résumé

BACKGROUND
The efficacy and added benefit of platinum-based chemotherapy (PtCT) for metastatic breast cancer (MBC) remain unclear in patients with and without germline BRCA1 or BRCA2 mutations (gBRCA1/2m and gBRCA1/2wt, respectively).
METHODS
We selected from the French national real-world multicentre ESME cohort (2008-2016) all patients with HER2-negative MBC with known gBRCA1/2 status at first-line chemotherapy initiation. Using multivariable Cox models, we compared the outcome (progression-free (PFS) and overall survival (OS)) of first-line PtCT and non-PtCT regimens based on the patients' gBRCA1/2 status and tumour subtype.
RESULTS
Patients who received PtCT had more aggressive tumour features. In the multivariable analysis, first-line PtCT was associated with better adjusted PFS and OS in gBRCA1/2m carriers (N = 300), compared with non-PtCT (HR 0.54, 95% CI 0.4-0.73, P < 0.001, and HR 0.70, 95% CI 0.49-0.99, P = 0.047, respectively). Conversely, outcomes were similar in gBRCA1/2wt patients (N = 922) treated with PtCT and non-PtCT, whatever the tumour subtype. Landmark analyses at months 3 and 6 post treatment initiation supported these results.
CONCLUSIONS
In this pre-PARP inhibitor real-world cohort, PFS and OS were better after PtCT than non-PtCT in patients with gBRCA1/2m, but not in those with gBRCA1/2wt. These results emphasise the need of early gBRCA1/2 testing in patients with MBC.
CLINICAL TRIAL NUMBER
NCT03275311.

Identifiants

pubmed: 36207609
doi: 10.1038/s41416-022-02003-1
pii: 10.1038/s41416-022-02003-1
pmc: PMC9681869
doi:

Substances chimiques

Antineoplastic Agents 0
BRCA1 Protein 0
BRCA1 protein, human 0
Platinum 49DFR088MY

Banques de données

ClinicalTrials.gov
['NCT03275311']

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1963-1973

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Nature Limited.

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Auteurs

William Jacot (W)

Institut du Cancer de Montpellier (ICM), INSERM U1194, Montpellier University, Montpellier, 34298, France. William.Jacot@icm.unicancer.fr.

Amélie Lusque (A)

Institut Claudius Regaud-IUCT Oncopole, Toulouse, France.

Cécile Vicier (C)

Department of Medical Oncology, Institut Paoli-Calmettes, Marseille, France.

Audrey Mailliez (A)

Centre Oscar Lambret, Lille, France.

Thibault de La Motte Rouge (T)

Centre Eugène Marquis, Rennes, France.

Luc Cabel (L)

Institut Curie-UMR 144-CNRS, Paris, France.

Christelle Levy (C)

Centre François Baclesse, Caen, France.

Anne Patsouris (A)

Institut de Cancérologie de l'Ouest, Pays de Loire, Angers, France.

Isabelle Desmoulins (I)

Centre Georges François Leclerc, Dijon, France.

Lionel Uwer (L)

Institut de Cancérologie de Lorraine-Alexis Vautrin, Vandoeuvre-lès-Nancy, France.

Jean-Christophe Thery (JC)

Centre Henri Becquerel, Rouen, France.

Mathieu Robain (M)

UNICANCER, Paris, France.

Olivier Caron (O)

Gustave Roussy, Villejuif, France.

Olivier Tredan (O)

Centre Léon Berard, Lyon, France.

Thomas Filleron (T)

Institut Claudius Regaud-IUCT Oncopole, Toulouse, France.

Jean-Sébastien Frenel (JS)

Institut de Cancérologie de l'Ouest, Saint Herblain, France.

Suzette Delaloge (S)

Gustave Roussy, Villejuif, France.

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