Veliparib: a new therapeutic option in ovarian cancer?
Administration, Oral
Benzimidazoles
/ pharmacology
Clinical Trials, Phase II as Topic
DNA Breaks, Single-Stranded
DNA Repair
/ drug effects
Female
Humans
Ovarian Neoplasms
/ drug therapy
Poly (ADP-Ribose) Polymerase-1
/ antagonists & inhibitors
Poly(ADP-ribose) Polymerase Inhibitors
/ pharmacology
Poly(ADP-ribose) Polymerases
/ metabolism
Synthetic Lethal Mutations
Treatment Outcome
BRCA mutations
BRCA-mutated ovarian cancer
PARP inhibitors
maintenance treatment
ovarian cancer
poly (ADP-ribose) polymerase inhibitors
veliparib
Journal
Future oncology (London, England)
ISSN: 1744-8301
Titre abrégé: Future Oncol
Pays: England
ID NLM: 101256629
Informations de publication
Date de publication:
Jun 2019
Jun 2019
Historique:
pubmed:
11
5
2019
medline:
7
1
2020
entrez:
11
5
2019
Statut:
ppublish
Résumé
The role of poly ADP ribose polymerase inhibitors in ovarian cancer is rapidly evolving. Three different poly ADP ribose polymerase inhibitors (olaparib, niraparib and rucaparib) have been already approved as maintenance after response to platinum-based chemotherapy; two of them (olaparib and rucaparib) also as single agents. Veliparib, a novel PARPI, showed promising results in preclinical and early clinical settings. The aim of this review is to discuss veliparib's mechanisms of action, to provide a clinical update on its safety and activity in ovarian cancer, and to highlight future perspectives for its optimal use. Veliparib favorable toxicity profile encourages its use either as monotherapy or in combination. Its peculiar neuroprotective and radio-sensitizing effect warrant further investigation.
Identifiants
pubmed: 31074636
doi: 10.2217/fon-2018-0883
doi:
Substances chimiques
Benzimidazoles
0
Poly(ADP-ribose) Polymerase Inhibitors
0
veliparib
01O4K0631N
PARP1 protein, human
EC 2.4.2.30
PARP2 protein, human
EC 2.4.2.30
Poly (ADP-Ribose) Polymerase-1
EC 2.4.2.30
Poly(ADP-ribose) Polymerases
EC 2.4.2.30
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM