Prise en charge médicale de la récidive du cancer épithélial de l'ovaire: Medical management of recurrent epithelial ovarian cancer.
Antibodies, Monoclonal, Humanized
/ therapeutic use
Antineoplastic Agents, Immunological
/ therapeutic use
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Azepines
/ therapeutic use
Bevacizumab
/ therapeutic use
Carcinoma, Ovarian Epithelial
/ drug therapy
Female
Genes, BRCA1
Genes, BRCA2
Humans
Immunoconjugates
/ therapeutic use
Immunotherapy
Isoxazoles
/ therapeutic use
Maintenance Chemotherapy
/ methods
Maytansine
/ analogs & derivatives
Neoplasm Recurrence, Local
/ drug therapy
Ovarian Neoplasms
/ drug therapy
Platinum Compounds
/ therapeutic use
Poly(ADP-ribose) Polymerase Inhibitors
/ therapeutic use
Pteridines
/ therapeutic use
Pyrazines
/ therapeutic use
Pyrimidines
/ therapeutic use
Bevacizumab
Bévacizumab
Cancer de l’ovaire
Early relapse
Inhibiteurs de PARP
Late relapse
Ovarian cancer
PARP inhibitors
Platine résistant
Platine sensible
Platinum-resistant
Platinum-sensitive
Rechute précoce
Rechute tardive
Journal
Bulletin du cancer
ISSN: 1769-6917
Titre abrégé: Bull Cancer
Pays: France
ID NLM: 0072416
Informations de publication
Date de publication:
Dec 2021
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-S32Informations de copyright
Copyright © 2021 Société FranÇaise du Cancer. Publié par Elsevier Masson SAS. Tous droits réservés.