Epithelioid hemangio-endothelioma (EHE) in NETSARC: The nationwide series of 267 patients over 12 years.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
10 2023
Historique:
received: 06 04 2023
revised: 07 07 2023
accepted: 24 07 2023
medline: 18 9 2023
pubmed: 26 8 2023
entrez: 25 8 2023
Statut: ppublish

Résumé

A NATIONWIDE STUDY: Epithelioid hemangioendothelioma (EHE) is an ultrarare sarcoma whose natural history and treatment is not well defined. We report on the presentation and outcome of 267 patients with EHE in the NETSARC+ network since 2010 in France. NETSARC (netsarc.org) is a network of 26 reference sarcoma centres with specialised multidisciplinary tumour boards (MDTB), funded by the French National Cancer Institute (NCI), Institut National du Cancer (INCA). Since 2010, presentation to an MDTB and second pathological review are mandatory for sarcoma patients. Patients' characteristics are collected in a nationwide database regularly monitored with stable incidence since 2013. The characteristics of patients with EHE at diagnosis are presented as well as progression-free survival (PFS), overall survival (OS), and outcome under treatment. Two hundred and sixty-seven patients with EHE were included in the NETSARC+ database since 2010. Median age in the series was 51 (range 10-90) years, 58% were women. Median tumour size was 37 mm (4-220). Forty-eight percent, 42%, and 10% were visceral, soft parts, or bone primaries. The most frequent sites were liver (28%), lung (13%). 40% were reported to have systemic (i.e. multifocal or metastatic disease) at diagnosis. With a median follow-up of 20 months, OS and PFS rates at 24 months were 82% and 67%, with 10-year projected OS and PFS of 62% and 21% respectively. Male and M+ patients at diagnosis had a significantly worse OS, but not PFS. Local treatment was associated with a favourable survival in localised but not in patients with advanced stage at diagnosis. For 23 patients receiving medical treatment, PFS and OS were 50.2% and 33.2% at 60 months were respectively. EHE is a frequently metastatic sarcoma at diagnosis with a unique natural history. This study shows in a nationwide series over 12 years that most patients progressed but are still alive at 10 years, both in localised and metastatic stages.

Identifiants

pubmed: 37625241
pii: S0959-8049(23)00364-7
doi: 10.1016/j.ejca.2023.113262
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

113262

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

J Y Blay (JY)

Department of Medical oncology, Centre Léon Bérard and Université Claude Bernard, Lyon, France. Electronic address: jean-yves.blay@lyon.unicancer.fr.

S Piperno-Neumann (S)

Department of Medical Oncology, Institut Curie and INSERM U830, Institut Curie Research Center, Paris, France.

S Watson (S)

Department of Medical Oncology, Institut Curie and INSERM U830, Institut Curie Research Center, Paris, France.

A Dufresne (A)

Department of Medical oncology, Centre Léon Bérard and Université Claude Bernard, Lyon, France.

T Valentin (T)

Department of Medical oncology, Institut Claudius Regaud and Institut Universitaire de Cancerologie, Oncopole, Toulouse, France.

F Duffaud (F)

Department of Medical oncology, La Timone University Hospital, Marseille, France.

M Toulmonde (M)

Departement of Medical Oncology, Institut Bergonié, Bordeaux, France.

A Italiano (A)

Departement of Medical Oncology, Institut Bergonié, Bordeaux, France.

F Bertucci (F)

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

C Tlemsani (C)

Department of Medical oncology, Hôpital Cochin-Saint-Vincent de Paul, Paris, France.

N Firmin (N)

Department of Medical oncology, Institut de Cancérologie de Montpellier, Montpellier, France.

E Bompas (E)

Department of Medical Oncology, Institut de Cancerologie Ouest, Nantes, France.

C Perrin (C)

Department of Medical oncology, Eugene Marquis Comprehensive Cancer Center and CHU, Rennes, France.

M Ropars (M)

Department of Medical oncology, Eugene Marquis Comprehensive Cancer Center and CHU, Rennes, France.

E Saada-Bouzid (E)

Department of Medical oncology, Centre Antoine-Lacassagne, Nice, France.

P Dubray-Longeras (P)

Department of Medical oncology, Centre Georges François Leclerc, Dijon, France.

A Hervieu (A)

Department of Medical oncology, Centre Jean Perrin/ERTICa EA 4677, Clermont-Ferrand, France.

C Lebbe (C)

Department of Medical oncology, Oncology Unit, Saint Louis Hospital, Paris, France.

J Gantzer (J)

Department of Medicine, ICANS, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.

L Chaigneau (L)

Department of Medical oncology, CHU Besancon, Besançon, France.

F Fiorenza (F)

Department of Medical oncology, CHU Limoges, Limoges, France.

M Rios (M)

Department of Medical oncology, Institut Cancerologie Lorraine, Centre Alexis Vautrin, Nancy, France.

N Isambert (N)

Department of Medical oncology, CHU, Poitiers, France.

P Soibinet (P)

Department of Medical oncology, Institut J Godinot Reims, Reims, France.

P Boudou-Roquette (P)

Department of Medical oncology, Hôpital Cochin-Saint-Vincent de Paul, Paris, France.

B Verret (B)

Department of Medical oncology, Gustave Roussy Cancer Campus, Villejuif, France.

G Ferron (G)

Department of Medical oncology, Institut Claudius Regaud and Institut Universitaire de Cancerologie, Oncopole, Toulouse, France.

T Ryckewaert (T)

Department of Medical oncology, Centre Oscar Lambret, and Université de Lille ULR 2694, Lille, France.

L Lebellec (L)

Department of Medical oncology, Centre Oscar Lambret, and Université de Lille ULR 2694, Lille, France.

M Brahmi (M)

Department of Medical oncology, Centre Léon Bérard and Université Claude Bernard, Lyon, France.

F Gouin (F)

Department of Medical oncology, Centre Léon Bérard and Université Claude Bernard, Lyon, France.

P Meeus (P)

Department of Medical oncology, Centre Léon Bérard and Université Claude Bernard, Lyon, France.

G Vaz (G)

Department of Medical oncology, Centre Léon Bérard and Université Claude Bernard, Lyon, France.

F Le Loarer (F)

Departement of Medical Oncology, Institut Bergonié, Bordeaux, France.

M Karanian (M)

Department of Medical oncology, Centre Léon Bérard and Université Claude Bernard, Lyon, France.

G De Pinieux (G)

Department of Medical oncology, CHU Tours, Tours, France.

F Ducimetiere (F)

Department of Medical oncology, Centre Léon Bérard and Université Claude Bernard, Lyon, France.

C Chemin (C)

Department of Medical oncology, Centre Léon Bérard and Université Claude Bernard, Lyon, France.

M Morelle (M)

Department of Medical oncology, Centre Léon Bérard and Université Claude Bernard, Lyon, France.

A Le Cesne (A)

Department of Medical oncology, Gustave Roussy Cancer Campus, Villejuif, France.

N Penel (N)

Department of Medical oncology, Centre Oscar Lambret, and Université de Lille ULR 2694, Lille, France.

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