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Open AccessJournal ArticleDOI

Rucaparib maintenance treatment for recurrent ovarian carcinoma after response to platinum therapy (ARIEL3): a randomised, double-blind, placebo-controlled, phase 3 trial

Robert L. Coleman, +116 more
- 28 Oct 2017 - 
- Vol. 390, Iss: 10106, pp 1949-1961
TLDR
This trial assessed rucaparib versus placebo after response to second-line or later platinum-based chemotherapy in patients with high-grade, recurrent, platinum-sensitive ovarian carcinoma harbouring a BRCA mutation or high percentage of genome-wide loss of heterozygosity.
About
This article is published in The Lancet.The article was published on 2017-10-28 and is currently open access. It has received 1139 citations till now. The article focuses on the topics: Rucaparib & Recurrent Ovarian Carcinoma.

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Citations
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Journal ArticleDOI

Biomarker-Guided Development of DNA Repair Inhibitors.

TL;DR: This work examines the development of selective agents targeting DNA repair, including PARP inhibitors; inhibitors of the DNA damage kinases ataxia-telangiectasia and Rad3 related (ATR), CHK1, WEE1, and atAXia- telangiECTasia mutated (ATM); and inhibitors of classical non-homologous end joining (cNHEJ and alternative end joining) and Alt EJ.
Journal ArticleDOI

Moving From Poly (ADP-Ribose) Polymerase Inhibition to Targeting DNA Repair and DNA Damage Response in Cancer Therapy

TL;DR: The most recent evidence for the clinical effect of PARP inhibition in breast and ovarian cancer is reviewed and expansion into the first-line setting and into other tumor types is explored.
Journal ArticleDOI

PARP Inhibition in Cancer: An Update on Clinical Development

TL;DR: Benefit appears to be strongest in a distinct population of patients with BRCA mutations or other defects in homologous recombination repair, and combination therapies, which include anti-angiogenesis agents and immunotherapy, show promise as a strategy to broaden efficacy for unselected patients.
Journal ArticleDOI

The DNA Damaging Revolution: PARP Inhibitors and Beyond.

TL;DR: Clinical progress made in the development of PARP inhibitors is detailed, rational combinations are reviewed, and the developed of emerging inhibitors against novel DDR targets, including DNA repair proteins, DNA damage signaling, and DNA metabolism are discussed.
Journal ArticleDOI

PARP inhibitors in ovarian cancer.

TL;DR: The future perspective of combination regimens with antiangiogenic, immunocheckpoint inhibitors, and other biological agents are anticipated as strategies to overcome resistance mechanisms, potentiate the therapeutic efficacy, and expand their clinical use in non-HR deficient tumors.
References
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Journal ArticleDOI

Niraparib Maintenance Therapy in Platinum-Sensitive, Recurrent Ovarian Cancer

TL;DR: Among patients with platinum-sensitive, recurrent ovarian cancer, the median duration of progression-free survival was significantly longer amongThose receiving niraparib than among those receiving placebo, regardless of the presence or absence of gBRCA mutations or HRD status, with moderate bone marrow toxicity.
Journal ArticleDOI

Olaparib tablets as maintenance therapy in patients with platinum-sensitive, relapsed ovarian cancer and a BRCA1/2 mutation (SOLO2/ENGOT-Ov21): a double-blind, randomised, placebo-controlled, phase 3 trial

Eric Pujade-Lauraine, +110 more
- 01 Sep 2017 - 
TL;DR: Olaparib tablet maintenance treatment provided a significant progression-free survival improvement with no detrimental effect on quality of life in patients with platinum-sensitive, relapsed ovarian cancer and a BRCA1/2 mutation.
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Integrated genomic analyses of ovarian carcinoma

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