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olaparib
Known as:
4-(3-{[4-(cyclopropylcarbonyl)piperazin-1-yl]carbonyl}-4-fluorobenzyl)phthalazin-1(2H)-one
A substance being studied in the treatment of breast, ovarian, and prostate cancers caused by mutations (changes) in the BRCA1 and BRCA2 genes. It is…
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National Institutes of Health
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Related topics
Related topics
12 relations
Narrower (3)
AZD 2281
Lynparza
PARP Inhibitor AZD2281
Broader (4)
Antineoplastic Agents
Phthalazines
Piperazines
Poly(ADP-ribose) Polymerase Inhibitors
NCIt Antineoplastic Agent Terminology
PARP1 protein, human
Poly(ADP-Ribose) Polymerase Inhibitors [MoA]
olaparib 50 MG Oral Capsule
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
A phase III study comparing single-agent olaparib or the combination of cediranib and olaparib to standard platinum-based chemotherapy in recurrent platinum-sensitive ovarian cancer.
Joyce F. Liu
,
M. Brady
,
+17 authors
M. Bookman
2020
Corpus ID: 219775630
6003Background: Combination cediranib (C) and olaparib (O) improved progression-free survival (PFS) in patients (pts) with…
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2019
2019
Randomized phase II CLIO study on olaparib monotherapy versus chemotherapy in platinum-resistant ovarian cancer.
A. Vanderstichele
,
E. Van Nieuwenhuysen
,
+7 authors
I. Vergote
Journal of Clinical Oncology
2019
Corpus ID: 190899576
5507 Background: The CLIO trial (NCT02822157) evaluated olaparib single-agent therapy versus standard of care chemotherapy in…
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Highly Cited
2016
Highly Cited
2016
Phase II trial of the oral PARP inhibitor olaparib (AZD2281) in BRCA-deficient advanced ovarian cancer.
M. Audeh
,
R. Penson
,
+6 authors
A. Tutt
Journal of Clinical Oncology
2016
Corpus ID: 6725423
5500 Background: Olaparib (AZD2281; KU-0059436) is a novel, orally active PARP inhibitor that induces synthetic lethality in…
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2015
2015
PARP inhibitor maintenance therapy for patients with platinum-sensitive recurrent ovarian cancer: a cost-effectiveness analysis.
H. Smith
,
Christen L. Walters Haygood
,
R. Arend
,
C. Leath
,
J. Straughn
Gynecologic Oncology
2015
Corpus ID: 11895966
2014
2014
Indoleamine 2,3-dioxygenase mediates immune-independent human tumor cell resistance to olaparib, gamma radiation, and cisplatin
S. M. Vareki
,
M. Rytelewski
,
+6 authors
J. Koropatnick
OncoTarget
2014
Corpus ID: 7373499
Indoleamine 2,3-dioxygenase-1 (IDO) is an immunosuppressive molecule expressed by most human tumors. IDO levels correlate with…
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2013
2013
PARP inhibitors bounce back
K. Garber
Nature reviews. Drug discovery
2013
Corpus ID: 2560499
A series of setbacks almost caused the demise of PARP inhibitors, but four companies are now beginning pivotal trials of these…
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2013
2013
Olaparib maintenance therapy in patients with platinum-sensitive relapsed serous ovarian cancer (SOC) and a BRCA mutation (BRCAm).
J. Ledermann
,
P. Harter
,
+14 authors
U. Matulonis
2013
Corpus ID: 220662978
5505 Background: Previously, we reported that maintenance treatment with the oral PARP inhibitor olaparib (400 mg bid) led to a…
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Highly Cited
2012
Highly Cited
2012
Phase I study to assess the safety and tolerability of olaparib in combination with bevacizumab in patients with advanced solid tumours
E. Dean
,
Mark R. Middleton
,
+4 authors
Malcolm R Ranson
British Journal of Cancer
2012
Corpus ID: 18692522
Background:Olaparib (AZD2281) is a potent oral poly(ADP-ribose) polymerase inhibitor with anti-tumour activity and acceptable…
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Review
2011
Review
2011
PARP inhibitors--current status and the walk towards early breast cancer.
J. Glendenning
,
A. Tutt
Breast
2011
Corpus ID: 3337985
2011
2011
Targeting the missing links for cancer therapy
K. Polyak
,
J. Garber
Nature Network Boston
2011
Corpus ID: 205377122
A continuing quest in clinical oncology is to effectively eliminate tumors without major side effects. But drugs rationally…
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