Recommandations pour la pratique clinique Nice/Saint-Paul-de-Vence 2022–2023 : Diagnostic histomoléculaire des carcinomes de l'endomètre.
Carcinome Classification Endometrial Instabilité Microsatellite Molecular Mutation POLE mutation Practice guidelines Recommandations carcinoma classification de l'endomètre du gène POLE instability micro-satellitaire moléculaire pratiques

Journal

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

Informations de publication

Date de publication:
Jun 2023
Historique:
medline: 13 8 2023
pubmed: 13 8 2023
entrez: 12 8 2023
Statut: ppublish

Résumé

French recommendations for clinical practice Nice-Saint-Paul de Vence 2022-2023: histomolecular diagnosis of endometrial carcinomas The characterisation of endometrial carcinomas has been recently modified and enriched by molecular classification, the integration of which now impacts therapeutic decisions on whether adjuvant therapy should be administered or not in localized tumors, and influences treatment selection in advanced disease. Mandatory information includes histological type according to WHO 2020 classification, histological grade, hormone receptors status and molecular classification, the main new elements to provide being analysis of MMR proteins, p53 status and POLE status in selected cases. Sampling and preparation of material must be performed adequately to allow complete analysis. Numerous markers can be used to better define histological type, distinguish between primary lesion or metastases, or provide prognostic information. Determination of MMR/MSI profile is complex but well defined by guidelines that precisely describe techniques to be used and interpretation rules. Knowledge of POLE status is useful to guide therapeutic strategy, especially to consider de-escalation in stages I and II, in particular in case of high grade and/or p53 mutated tumors. This is why indications of POLE determination must be well defined. Finally, oncogenetics consultation is recommended in dMMR tumors (except in case or MLH1 promoter methylation) and in patients with evocative familial history.

Identifiants

pubmed: 37573035
pii: S0007-4551(23)00330-2
doi: 10.1016/S0007-4551(23)00330-2
pii:
doi:

Types de publication

English Abstract Journal Article

Langues

fre

Sous-ensembles de citation

IM

Pagination

6S10-6S19

Informations de copyright

Copyright © 2023 Elsevier Masson SAS. Tous droits réservés. All rights reserved.

Auteurs

Corinne Jeanne (C)

Laboratoire d'anatomie et cytologie pathologiques, CLCC Baclesse, 14000 Caen, France. Electronic address: c.jeanne@baclesse.unicancer.fr.

Isabelle Treilleux (I)

Laboratoire d'anatomie et cytologie pathologiques, CLCC Léon-Bérard, 69008 Lyon, France.

Marie-Aude Le Frère-Belda (MA)

Laboratoire d'anatomie et cytologie pathologiques, hôpital européen Georges-Pompidou, 75015 Paris, France.

Jérôme Alexandre (J)

Service d'oncologie médicale, AP-HP Centre, université de Paris, site Cochin, 123, boulevard de Port-Royal, 75014 Paris, France.

Florence Joly (F)

Département de médecine, université de Caen, centre François-Baclesse, 3, avenue du Général-Harris, 14000 Caen, France.

Etienne Rouleau (E)

Laboratoire de génétique moléculaire, CLCC Institut Gustave-Roussy, 94805 Villejuif, France.

Classifications MeSH