Prise en charge médicale de la récidive du cancer épithélial de l'ovaire: Medical management of recurrent epithelial ovarian cancer.


Journal

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

Informations de publication

Date de publication:
Dec 2021
Historique:
entrez: 27 12 2021
pubmed: 28 12 2021
medline: 8 1 2022
Statut: ppublish

Résumé

The panel of therapeutic options available for medical treatment of relapsed ovarian cancer increased over the last years. In late, platinum-sensitive relapse, standard treatment remains platinum-based polychemotherapy. The choice between bevacizumab added to chemotherapy followed by maintenance and inhibitors of poly-(ADP-riboses) polymerases (PARPi) after response to platinum-based therapy should be discussed, taking into account prior treatment, contraindications, and disease characteristics (biology, symptoms…). The addition of bevacizumab at first platinum-sensitive relapse can be considered if it has not been administered in first line, and it is optional (rechallenge) if previously administered (but without Marketing Authorization in this setting). PARPi are indicated for maintenance therapy after response to platinum-based chemotherapy (whatever the treatment line), regardless of BRCA mutational status, in case of no prior administration. Early relapses are associated with poor prognosis and therapeutic options are more limited. They are treated by monochemotherapy without platinum agents, associated with bevacizumab if not administered previously. Beyond first early relapse, there is no standard and inclusion in a clinical trial should be proposed if possible. Several clinical studies assessing associations of immunotherapy and chemotherapy and/or antiangiogenic drugs and/or targeted therapies (such as PARPi) are ongoing in early or late relapse.

Identifiants

pubmed: 34955159
pii: S0007-4551(21)00584-1
doi: 10.1016/S0007-4551(21)00584-1
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Antineoplastic Agents, Immunological 0
Azepines 0
BI 6727 0
Immunoconjugates 0
Isoxazoles 0
MLN 8237 0
Platinum Compounds 0
Poly(ADP-ribose) Polymerase Inhibitors 0
Pteridines 0
Pyrazines 0
Pyrimidines 0
Maytansine 14083FR882
Bevacizumab 2S9ZZM9Q9V
mirvetuximab soravtansine 98DE7VN88D
pembrolizumab DPT0O3T46P
berzosertib L423PRV3V3

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

S22-S32

Informations de copyright

Copyright © 2021 Société FranÇaise du Cancer. Publié par Elsevier Masson SAS. Tous droits réservés.

Auteurs

Patricia Pautier (P)

Département d'oncologie médicale, institut Gustave-Roussy, Villejuif, France. Electronic address: patricia.pautier@gustaveroussy.fr.

Thibault de la Motte-Rouge (T)

Département de médecine, centre Eugène-Marquis, avenue de la Bataille-FlandresDunkerque, Rennes, France.

Fabrice Lécuru (F)

Service de chirurgie sénologique, gynécologique et reconstructrice, institut Curie, 26 rue d'Ulm, Paris, France ; Faculté de médecine, Université de Paris, Paris, France.

Jean-Marc Classe (JM)

Service de chirurgie oncologique, institut de cancérologie de l'Ouest, France ; Faculté de médecine, université de Nantes, Nantes, France.

Gwenaël Ferron (G)

Département de chirurgie oncologique, institut Claudius-Regaud - IUCT Toulouse, France ; INSERM CRCT 19 (Oncogenèse des sarcomes), centre de recherches en cancérologie de Toulouse, 2, avenue Hubert-Curien, Toulouse, France.

Anne Floquet (A)

Département d'oncologie médicale, Institut Bergonié, 229 cours Agonne, Bordeaux, France.

J E Kurtz (JE)

Pôle d'oncologie médico-chirurgicale et d'hématologie, ICANS-Europe, Strasbourg, France.

Gilles Freyer (G)

Service d'oncologie médicale, institut de cancérologie des HCL ; Université Lyon 1, Lyon, France.

Anne-Claire Hardy-Bessard (AC)

Centre armoricain d'oncologie, CARIO HPCA, 10, rue François-Jacob, Plérin, France.

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Classifications MeSH