Abk�rzung zur Hauptnavigation Abk�rzung zu den Newsmeldungen Abk�rzung zu den Topstories  
  Barrierefreiheit    Kontakt MedUni Wien    Intranet    MedUni Wien - Shop    Universitätsbibliothek    Universitätsklinikum AKH Wien  
 
ccc_logo_en.gif
 
AKH Wien
 
 
Hauptnavigation
  • Livestream 2021
  • Home
  • Über das CCC
    • Allgemeines
    • Leitung der Organisationseinheit
    • CCC-Office Team
    • Kliniken und Partner
    • Qualitätsmanagement
    • Kontakt
  • PatientInnen
    • Covid-19
    • Allgemeines
    • Cancer School
    • Terminvereinbarung
    • Pflegeambulanz
    • PatientInnenvertretung
    • Links
  • Klinischer Bereich
    • Allgemeines
    • CCC Tumorboards
  • Wissenschaft & Forschung
    • Young CCC
    • CCC-ExpertInnenvideos
    • CCC Forschungscluster
    • CCC Units
    • CCC Platforms
    • Translationale Forschung
    • CCC Best Paper Award
    • CCC-TRIO Symposium
    • Kontakt/Links
  • Lehre
    • CCC Cancer School
    • Vienna International Summer School on Clinical and Experimental Oncology - VSSO
    • CCC Excellence Lecture
    • Interdisziplinäre onkologische Ausbildung
    • Klinisch-Praktisches Jahr (KPJ)
    • PhD Programme
    • Postgraduelle Fort- und Weiterbildung
    • Information/Contact
 
 
Subnavigation
    Inhaltsbereich


    Zurück zur Übersicht
    Gynecologic oncology. 2015 Dec 29. pii: S0090-8258(15)30230-4. doi: 10.1016/j.ygyno.2015.12.027
    BRCA1/2 mutations associated with progression-free survival in ovarian cancer patients in the AGO-OVAR 16 study.
    Harter P1,  Johnson T2,  Berton-Rigaud D3,  Park SY4,  Friedlander M5,  Del Campo JM6,  Shimada M7,  Forget F8,  Mirza MR9,  Colombo N10,  Zamagni C11,  Chan JK12,  Imhof M13,  Herzog TJ14,  O'Donnell D15,  Heitz F16,  King K17,  Stinnett S18,  Barrett C19,  Jobanputra M20,  Xu CF21,  du Bois A22
    Author information
    1Department of Gynecology & Gynecologic Oncology, Kliniken Essen Mitte, Essen, Germany. Electronic address: p.harter@gmx.de.
    2GlaxoSmithKline, Gunnels Wood Road, Stevenage SG1 2NY, UK.
    3Institut de Cancérologie de l'Ouest, Centre René Gauducheau, Saint-Herblain, France.
    4National Cancer Center, Goyang, Republic of Korea.
    5The Prince of Wales Clinical School University of New South Wales, Randwick, NSW, Australia.
    6Department of Medical Oncology, Vall d'Hebron University Hospital, Barcelona, Spain.
    7Department of Obstetrics and Gynecology, Tottori University School of Medicine, Nishimachi, Yonago, Japan.
    8Centre Hospitalier de l'Ardenne, Libramont, Belgium.
    9Department of Oncology, Rigshospitalet, Copenhagen, Denmark.
    10Gynecologic Oncology, University of Milan-Bicocca and European Institute of Oncology, Milan, Italy.
    11S. Orsola-Malpighi University Hospital, Bologna, Italy.
    12California Pacific and Palo Alto Sutter Cancer Research Institute, San Francisco, CA, USA.
    13Regional Hospital Korneuburg, Medical University of Vienna, Austria.
    14University of Cincinnati Cancer Institute, Cincinnati, OH, USA.
    15All Ireland Cooperative Oncology Research Group, Dublin, Ireland.
    16Department of Gynecology & Gynecologic Oncology, Kliniken Essen Mitte, Essen, Germany.
    17Parexel International, Durham, NC, USA.
    18Parexel International, Durham, NC, USA.
    19Novartis Pharma AG, Basel, Switzerland.
    20Biogen Idec, Berkshire, UK.
    21GlaxoSmithKline, Gunnels Wood Road, Stevenage SG1 2NY, UK.
    22Department of Gynecology & Gynecologic Oncology, Kliniken Essen Mitte, Essen, Germany.
    Abstract

    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.

    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.

    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 14.1months, 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 17.7months, 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 14.1months, 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).

    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.


    Copyright © 2015. Published by Elsevier Inc.

    KEYWORDS: GWAS, Germline BRCA mutation, Ovarian cancer, Pazopanib, Progression-free survival

    Publikations ID: 26740259
    Quelle: öffnen
     
    Drucken
     
    ccc_logo_en.gif
    ccc_logo_en.gif
    ccc_logo_en.gif

    Schnellinfo

     
    -- Initiative Krebsforschung / Krebsforschungslauf

    -- Cancer Care
    -- Kliniken und Partner
    -- CCC Cancer School
    -- Young CCC
    -- CCC Tumorboards
    -- CCC Forschungscluster
    -- CCC Units
    -- CCC Platforms
    -- SOPs / Leitlinien
    -- Kontakt
    Zuklappen
     
    Ausklappen
     
     

    Featured

     
     
     
     
     
     
     
     
     
     
     
     
     
    © MedUni Wien |
     Impressum | Nutzungsbedingungen | Kontakt