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BRCA1/2 mutations associated with progression-free survival in ovarian cancer patients in the AGO-OVAR 16 study.

Identifieur interne : 002276 ( PubMed/Checkpoint ); précédent : 002275; suivant : 002277

BRCA1/2 mutations associated with progression-free survival in ovarian cancer patients in the AGO-OVAR 16 study.

Auteurs : Philipp Harter [Allemagne] ; Toby Johnson [Royaume-Uni] ; Dominique Berton-Rigaud [France] ; Sang-Yoon Park [Corée du Sud] ; Michael Friedlander [Australie] ; Josep M. Del Campo [Espagne] ; Muneaki Shimada [Japon] ; Frédéric Forget [Belgique] ; Mansoor R. Mirza [Danemark] ; Nicoletta Colombo [Italie] ; Claudio Zamagni [Italie] ; John K. Chan [États-Unis] ; Martin Imhof [Autriche] ; Thomas J. Herzog [États-Unis] ; Dearbhaile O'Donnell [Irlande (pays)] ; Florian Heitz [Allemagne] ; Karen King [États-Unis] ; Sandy Stinnett [États-Unis] ; Catherine Barrett [Suisse] ; Minesh Jobanputra [Royaume-Uni] ; Chun-Fang Xu [Royaume-Uni] ; Andreas Du Bois [Allemagne]

Source :

RBID : pubmed:26740259

Descripteurs français

English descriptors

Abstract

AGO-OVAR 16 demonstrated that pazopanib maintenance therapy significantly increased progression-free survival (PFS) in patients with ovarian cancer whose disease had not progressed after first-line therapy. In a sub-study, we evaluated the effect of clinically important germline BRCA1 and BRCA2 mutations on PFS.

DOI: 10.1016/j.ygyno.2015.12.027
PubMed: 26740259


Affiliations:


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pubmed:26740259

Le document en format XML

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<name sortKey="King, Karen" sort="King, Karen" uniqKey="King K" first="Karen" last="King">Karen King</name>
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<name sortKey="Barrett, Catherine" sort="Barrett, Catherine" uniqKey="Barrett C" first="Catherine" last="Barrett">Catherine Barrett</name>
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<name sortKey="Jobanputra, Minesh" sort="Jobanputra, Minesh" uniqKey="Jobanputra M" first="Minesh" last="Jobanputra">Minesh Jobanputra</name>
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<name sortKey="Xu, Chun Fang" sort="Xu, Chun Fang" uniqKey="Xu C" first="Chun-Fang" last="Xu">Chun-Fang Xu</name>
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<title xml:lang="en">BRCA1/2 mutations associated with progression-free survival in ovarian cancer patients in the AGO-OVAR 16 study.</title>
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<name sortKey="Harter, Philipp" sort="Harter, Philipp" uniqKey="Harter P" first="Philipp" last="Harter">Philipp Harter</name>
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<nlm:affiliation>Department of Gynecology & Gynecologic Oncology, Kliniken Essen Mitte, Essen, Germany. Electronic address: p.harter@gmx.de.</nlm:affiliation>
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<name sortKey="Johnson, Toby" sort="Johnson, Toby" uniqKey="Johnson T" first="Toby" last="Johnson">Toby Johnson</name>
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<name sortKey="Berton Rigaud, Dominique" sort="Berton Rigaud, Dominique" uniqKey="Berton Rigaud D" first="Dominique" last="Berton-Rigaud">Dominique Berton-Rigaud</name>
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<name sortKey="Shimada, Muneaki" sort="Shimada, Muneaki" uniqKey="Shimada M" first="Muneaki" last="Shimada">Muneaki Shimada</name>
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<name sortKey="Forget, Frederic" sort="Forget, Frederic" uniqKey="Forget F" first="Frédéric" last="Forget">Frédéric Forget</name>
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<name sortKey="Mirza, Mansoor R" sort="Mirza, Mansoor R" uniqKey="Mirza M" first="Mansoor R" last="Mirza">Mansoor R. Mirza</name>
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<nlm:affiliation>Department of Oncology, Rigshospitalet, Copenhagen, Denmark.</nlm:affiliation>
<country xml:lang="fr">Danemark</country>
<wicri:regionArea>Department of Oncology, Rigshospitalet, Copenhagen</wicri:regionArea>
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<name sortKey="Colombo, Nicoletta" sort="Colombo, Nicoletta" uniqKey="Colombo N" first="Nicoletta" last="Colombo">Nicoletta Colombo</name>
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<nlm:affiliation>Gynecologic Oncology, University of Milan-Bicocca and European Institute of Oncology, Milan, Italy.</nlm:affiliation>
<country xml:lang="fr">Italie</country>
<wicri:regionArea>Gynecologic Oncology, University of Milan-Bicocca and European Institute of Oncology, Milan</wicri:regionArea>
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<name sortKey="Zamagni, Claudio" sort="Zamagni, Claudio" uniqKey="Zamagni C" first="Claudio" last="Zamagni">Claudio Zamagni</name>
<affiliation wicri:level="1">
<nlm:affiliation>S. Orsola-Malpighi University Hospital, Bologna, Italy.</nlm:affiliation>
<country xml:lang="fr">Italie</country>
<wicri:regionArea>S. Orsola-Malpighi University Hospital, Bologna</wicri:regionArea>
<wicri:noRegion>Bologna</wicri:noRegion>
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<name sortKey="Chan, John K" sort="Chan, John K" uniqKey="Chan J" first="John K" last="Chan">John K. Chan</name>
<affiliation wicri:level="2">
<nlm:affiliation>California Pacific and Palo Alto Sutter Cancer Research Institute, San Francisco, CA, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>California Pacific and Palo Alto Sutter Cancer Research Institute, San Francisco, CA</wicri:regionArea>
<placeName>
<region type="state">Californie</region>
</placeName>
</affiliation>
</author>
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<name sortKey="Imhof, Martin" sort="Imhof, Martin" uniqKey="Imhof M" first="Martin" last="Imhof">Martin Imhof</name>
<affiliation wicri:level="1">
<nlm:affiliation>Regional Hospital Korneuburg, Medical University of Vienna, Austria.</nlm:affiliation>
<country xml:lang="fr">Autriche</country>
<wicri:regionArea>Regional Hospital Korneuburg, Medical University of Vienna</wicri:regionArea>
<wicri:noRegion>Medical University of Vienna</wicri:noRegion>
</affiliation>
</author>
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<name sortKey="Herzog, Thomas J" sort="Herzog, Thomas J" uniqKey="Herzog T" first="Thomas J" last="Herzog">Thomas J. Herzog</name>
<affiliation wicri:level="2">
<nlm:affiliation>University of Cincinnati Cancer Institute, Cincinnati, OH, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>University of Cincinnati Cancer Institute, Cincinnati, OH</wicri:regionArea>
<placeName>
<region type="state">Ohio</region>
</placeName>
</affiliation>
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<name sortKey="O Donnell, Dearbhaile" sort="O Donnell, Dearbhaile" uniqKey="O Donnell D" first="Dearbhaile" last="O'Donnell">Dearbhaile O'Donnell</name>
<affiliation wicri:level="1">
<nlm:affiliation>All Ireland Cooperative Oncology Research Group, Dublin, Ireland.</nlm:affiliation>
<country xml:lang="fr">Irlande (pays)</country>
<wicri:regionArea>All Ireland Cooperative Oncology Research Group, Dublin</wicri:regionArea>
<wicri:noRegion>Dublin</wicri:noRegion>
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<name sortKey="Heitz, Florian" sort="Heitz, Florian" uniqKey="Heitz F" first="Florian" last="Heitz">Florian Heitz</name>
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<front>
<div type="abstract" xml:lang="en">AGO-OVAR 16 demonstrated that pazopanib maintenance therapy significantly increased progression-free survival (PFS) in patients with ovarian cancer whose disease had not progressed after first-line therapy. In a sub-study, we evaluated the effect of clinically important germline BRCA1 and BRCA2 mutations on PFS.</div>
</front>
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<Year>2016</Year>
<Month>02</Month>
<Day>24</Day>
</DateCreated>
<DateCompleted>
<Year>2016</Year>
<Month>06</Month>
<Day>28</Day>
</DateCompleted>
<DateRevised>
<Year>2016</Year>
<Month>02</Month>
<Day>24</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Electronic">1095-6859</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>140</Volume>
<Issue>3</Issue>
<PubDate>
<Year>2016</Year>
<Month>Mar</Month>
</PubDate>
</JournalIssue>
<Title>Gynecologic oncology</Title>
<ISOAbbreviation>Gynecol. Oncol.</ISOAbbreviation>
</Journal>
<ArticleTitle>BRCA1/2 mutations associated with progression-free survival in ovarian cancer patients in the AGO-OVAR 16 study.</ArticleTitle>
<Pagination>
<MedlinePgn>443-9</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1016/j.ygyno.2015.12.027</ELocationID>
<ELocationID EIdType="pii" ValidYN="Y">S0090-8258(15)30230-4</ELocationID>
<Abstract>
<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">AGO-OVAR 16 demonstrated that pazopanib maintenance therapy significantly increased progression-free survival (PFS) in patients with ovarian cancer whose disease had not progressed after first-line therapy. In a sub-study, we evaluated the effect of clinically important germline BRCA1 and BRCA2 mutations on PFS.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Of 940 AGO-OVAR 16 participants, 664 had BRCA1/2 exon sequencing data (pazopanib, n=335; placebo, n=329). A Cox model was used to test the association between genetic variants and PFS.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Ninety-seven of 664 patients (15%) carried clinically important BRCA1/2 mutations (BRCA1/2 carriers: pazopanib 14%, placebo 16%). Median PFS was longer in BRCA1/2 mutation carriers than in BRCA1/2 non-carriers in the placebo arm (30.3 vs 14.1 months, hazard ratio, 0.48; 95% confidence interval [CI]: 0.29-0.78; P=0.0031); a similar non-significant trend was noted with pazopanib (30.2 vs 17.7 months, hazard ratio, 0.64; 95% CI: 0.40-1.03; P=0.069). Among BRCA1/2 non-carriers, PFS was longer for pazopanib-treated patients than placebo-treated patients (17.7 vs 14.1 months, hazard ratio, 0.77; 95% CI: 0.62-0.97; P=0.024). Among BRCA1/2 carriers, there was no significant PFS difference between treatments, although numbers were small (pazopanib, 46; placebo, 51), resulting in a wide CI (hazard ratio, 1.36; 95% CI: 0.66-2.82).</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Patients with clinically important BRCA1/2 mutations had better prognosis. BRCA1/2 mutation status might be added as strata in future trials in primary ovarian cancer.</AbstractText>
<CopyrightInformation>Copyright © 2016 Elsevier Inc. All rights reserved.</CopyrightInformation>
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