Bevacizumab or PARP-Inhibitors Maintenance Therapy for Platinum-Sensitive Recurrent Ovarian Cancer: A Network Meta-Analysis.
Antineoplastic Agents, Immunological
/ therapeutic use
BRCA1 Protein
/ genetics
BRCA2 Protein
/ genetics
Bevacizumab
/ therapeutic use
Carboplatin
/ therapeutic use
Drug Resistance, Neoplasm
Female
Heterozygote
Humans
Mutation
Neoplasm Recurrence, Local
/ drug therapy
Ovarian Neoplasms
/ drug therapy
Poly(ADP-ribose) Polymerase Inhibitors
/ therapeutic use
PARP-inhibitors
bevacizumab
platinum-sensitive ovarian cancer
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
27 May 2020
27 May 2020
Historique:
received:
23
04
2020
revised:
19
05
2020
accepted:
22
05
2020
entrez:
31
5
2020
pubmed:
31
5
2020
medline:
17
2
2021
Statut:
epublish
Résumé
Targeted agents such as bevacizumab (BEV) or poly (ADP-ribose) polymerase inhibitors (PARPi) which have been added as concomitant or maintenance therapies have been shown to improve progression-free survival (PFS) in patients with platinum-sensitive recurrent ovarian cancer (PS rOC). In the absence of direct comparison, we performed a network meta-analysis considering We searched PubMed, EMBASE, and MEDLINE for trials involving patients with PS rOC treated with BEV or PARPi. Different comparisons were performed for patients included in the PARPi trials, according to In the overall population, PARPi prolonged PFS with respect to BEV (hazard ratio (HR) = 0.70, 95% CI 0.54-0.91). In the PARPi performed better as compared with BEV in terms of PFS for the treatment of PS rOC, especially in BRCAm patients who had not previously received PARPi.
Identifiants
pubmed: 32471250
pii: ijms21113805
doi: 10.3390/ijms21113805
pmc: PMC7312982
pii:
doi:
Substances chimiques
Antineoplastic Agents, Immunological
0
BRCA1 Protein
0
BRCA1 protein, human
0
BRCA2 Protein
0
BRCA2 protein, human
0
Poly(ADP-ribose) Polymerase Inhibitors
0
Bevacizumab
2S9ZZM9Q9V
Carboplatin
BG3F62OND5
Types de publication
Journal Article
Meta-Analysis
Langues
eng
Sous-ensembles de citation
IM
Déclaration de conflit d'intérêts
F.P. reports grants from AstraZeneca; grants, personal fees, and other from Roche; personal fees and other from Eli Lilly; personal fees from Amgen; personal fees from Ipsen; personal fees from MSD; personal fees from Takeda; grants and other from Eisai; other from Novartis and Pfizer, outside the submitted work. L.G. reports personal fees from Eli lilly, outside the submitted work. The other authors have nothing to disclose.
Références
Lancet. 2017 Oct 28;390(10106):1949-1961
pubmed: 28916367
Lancet Oncol. 2019 May;20(5):636-648
pubmed: 30948273
Lancet Oncol. 2015 Jan;16(1):87-97
pubmed: 25481791
N Engl J Med. 2019 Dec 19;381(25):2403-2415
pubmed: 31562800
Gynecol Oncol. 2019 Feb;152(2):416-425
pubmed: 30409489
Clin Cancer Res. 2020 Jun 1;26(11):2546-2555
pubmed: 32034076
Gynecol Oncol. 2017 Nov;147(2):267-275
pubmed: 28882436
N Engl J Med. 2018 Dec 27;379(26):2495-2505
pubmed: 30345884
J Clin Oncol. 2012 Jun 10;30(17):2039-45
pubmed: 22529265
CA Cancer J Clin. 2018 Nov;68(6):394-424
pubmed: 30207593
BMC Med Res Methodol. 2015 Jul 31;15:58
pubmed: 26227148
Lancet Oncol. 2017 Sep;18(9):1274-1284
pubmed: 28754483
Ann Oncol. 2019 May 1;30(5):672-705
pubmed: 31046081
Ann Oncol. 2017 Apr 1;28(4):727-732
pubmed: 27993805
N Engl J Med. 2016 Dec;375(22):2154-2164
pubmed: 27717299
Invest New Drugs. 2020 Feb;38(1):181-193
pubmed: 31650446
N Engl J Med. 2012 Apr 12;366(15):1382-92
pubmed: 22452356
Mol Cancer Res. 2019 Feb;17(2):409-419
pubmed: 30429212
Lancet Oncol. 2017 Jun;18(6):779-791
pubmed: 28438473
N Engl J Med. 2019 Dec 19;381(25):2416-2428
pubmed: 31851799
Diagnostics (Basel). 2019 Aug 01;9(3):
pubmed: 31374917
Res Synth Methods. 2012 Dec;3(4):312-24
pubmed: 26053424
Expert Opin Drug Saf. 2017 Jun;16(6):687-696
pubmed: 28471247
Adv Ther. 2019 Dec;36(12):3368-3380
pubmed: 31599396
Ann Oncol. 2013 Oct;24 Suppl 6:vi24-32
pubmed: 24078660
N Engl J Med. 2019 Dec 19;381(25):2391-2402
pubmed: 31562799
N Engl J Med. 2018 Aug 23;379(8):753-763
pubmed: 30110579