[Borderlines and malignant phyllodes tumors of the breast: From the anatomopathological challenge to the standard of care].

Tumeurs phyllodes borderlines et malignes du sein : du défi anatomopathologique à l’élaboration d’un standard de prise en charge.
Breast surgery Chirurgie du sein Histologie Histology Phyllode tumor Radiation therapy Radiothérapie Sarcoma Sarcome Tumeur phyllode

Journal

Bulletin du cancer
ISSN: 1769-6917
Titre abrégé: Bull Cancer
Pays: France
ID NLM: 0072416

Informations de publication

Date de publication:
05 Sep 2024
Historique:
received: 21 05 2024
revised: 19 07 2024
accepted: 24 07 2024
medline: 7 9 2024
pubmed: 7 9 2024
entrez: 6 9 2024
Statut: aheadofprint

Résumé

Phyllodes tumors, borderline (BPT) and malignant (MPT), represent a rare group of fibroepithelial breast tumors. Due to their rarity, their treatment remains poorly codified. The precise incidence of these tumors remains unknown. TPMs represent half of breast sarcomas and 1 % of breast tumors. Their treatment at the localized stage is based on surgery, that can be conservative surgery or a mastectomy. The impact of oncoplastic techniques and immediate breast reconstruction is not documented. The excision margins of the BPT and MPT must be free, a wider margin can provide a benefit in local recurrence but in also overall survival in the case of TPM. The optimal width of the excision margin is not known. In the event of positive margins, a second surgery could make up the result of an insufficient first surgery. Chemotherapy does not seem to provide any benefit on recurrence-free survival, but the available data are particularly weak. The data on adjuvant radiotherapy are more important. This allows better local control in the event of breast-conserving surgery. The benefit of post-mastectomy radiotherapy is less documented but can be considered in cases of poor prognostic factors. The management of TPM at the metastatic stage is based on the use of chemotherapy (anthracyclines, Ifosfamide) and local treatment of metastases in cases of oligometastatic disease. Due to the rarity of these tumors, it is essential that their management be discussed within a network of qualified professionals (NETSARC+).

Identifiants

pubmed: 39242253
pii: S0007-4551(24)00281-9
doi: 10.1016/j.bulcan.2024.07.006
pii:
doi:

Types de publication

English Abstract Journal Article Review

Langues

fre

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 Société Française du Cancer. Published by Elsevier Masson SAS. All rights reserved.

Auteurs

Mathias Neron (M)

Service de chirurgie oncologique, Institut du Cancer de Montpellier, Montpellier, France; IRCM, Inserm, ICM, université de Montpellier, Montpellier, France. Electronic address: mathias.neron@orange.fr.

Aurélie Maran Gonzalez (A)

Service d'anatomopathologie, Institut du Cancer de Montpellier, Montpellier, France.

Carmen Llacer (C)

Service de radiothérapie, Institut du Cancer de Montpellier, Montpellier, France.

Sébastien Carrere (S)

Service de chirurgie oncologique, Institut du Cancer de Montpellier, Montpellier, France.

Christophe Sajous (C)

Service d'oncologie médicale, hospices civils de Lyon, Lyon, France.

Nelly Firmin (N)

Service d'oncologie médicale, Institut du Cancer de Montpellier, Montpellier, France.

Classifications MeSH