Systemic treatment with or without ablative therapies in oligometastatic breast cancer: A single institution analysis of patient outcomes.


Journal

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

Informations de publication

Date de publication:
Feb 2023
Historique:
received: 18 10 2022
revised: 27 12 2022
accepted: 29 12 2022
pubmed: 30 1 2023
medline: 15 2 2023
entrez: 29 1 2023
Statut: ppublish

Résumé

Local ablative treatment (LAT) is increasingly combined with systemic therapy in oligometastatic breast cancer (OMBC), without a high-level evidence to support this strategy. We evaluated the addition of LAT to systemic treatment in terms of progression-free survival (PFS) and overall survival (OS). Secondary endpoints were local control (LC) and toxicity. We sought to identify prognostic factors associated with longer OS and PFS. We identified consecutive patients treated between 2014 and 2018 for synchronous or metachronous OMBC (defined as ≤ 5 metastases). LAT included stereotactic body radiation therapy (SBRT) and volumetric modulated arc therapy (VMAT), surgery, cryotherapy and percutaneous radiofrequency ablation (PRA). PFS and OS were calculated, and Cox regression models analyzed for potential predictors of survival. One hundred two patients were included (no-LAT, n = 62; LAT, n = 40). Sixty-four metastases received LAT. Median follow-up was 50.4 months (95% CI [44.4; 53.4]). One patient experienced grade 3 toxicity in the LAT group. Five-year PFS and OS were 34.75% (95% CI [24.42-45.26]) and 63.21% (95% CI [50.69-73.37]) respectively. Patients receiving both LAT and systemic therapy had longer PFS and OS than those with no-LAT ([HR 0.39, p = 0.002]) and ([HR 0.31, p = 0.01]). The use of LAT, HER2-positive status and hormone-receptor positivity were associated with longer PFS and OS whereas liver metastases led to worse PFS. LAT was associated with improved outcomes in OMBC when added to systemic treatment, without significantly increasing toxicity. The prognostic factors identified to extend PFS and OS may help guide clinicians in selecting patients for LAT.

Identifiants

pubmed: 36709639
pii: S0960-9776(22)00235-1
doi: 10.1016/j.breast.2022.12.035
pmc: PMC9982270
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

102-109

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.

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Auteurs

Gauthier Glemarec (G)

Department of Radiation Oncology, Institut Claudius Regaud, IUCT-O, Toulouse, France.

Jean-Louis Lacaze (JL)

Department of Medical Oncology, Institut Claudius Regaud, IUCT-O, Toulouse, France.

Bastien Cabarrou (B)

Biostatistics Unit, Institut Claudius Regaud, IUCT-O, Toulouse, France.

Richard Aziza (R)

Department of Radiology, Institut Claudius Regaud, IUCT-O, Toulouse, France.

Eva Jouve (E)

Department of Surgery, Institut Claudius Regaud, IUCT-O, Toulouse, France.

Slimane Zerdoud (S)

Department of Radiology, Institut Claudius Regaud, IUCT-O, Toulouse, France.

Eleonora De Maio (E)

Department of Medical Oncology, Institut Claudius Regaud, IUCT-O, Toulouse, France.

Carole Massabeau (C)

Department of Radiation Oncology, Institut Claudius Regaud, IUCT-O, Toulouse, France.

Maxime Loo (M)

Department of Radiation Oncology, Institut Claudius Regaud, IUCT-O, Toulouse, France.

Vincent Esteyrie (V)

Department of Radiation Oncology, Institut Claudius Regaud, IUCT-O, Toulouse, France.

Mony Ung (M)

Department of Medical Oncology, Institut Claudius Regaud, IUCT-O, Toulouse, France.

Florence Dalenc (F)

Department of Medical Oncology, Institut Claudius Regaud, IUCT-O, Toulouse, France.

Francoise Izar (F)

Department of Radiation Oncology, Institut Claudius Regaud, IUCT-O, Toulouse, France.

Ciprian Chira (C)

Department of Radiation Oncology, Institut Claudius Regaud, IUCT-O, Toulouse, France. Electronic address: chira.ciprian@iuct-oncopole.fr.

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