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Survival in epithelial ovarian cancer: a multivariate analysis incorporating BRCA mutation status and platinum sensitivity.
Gallagher, D J; Konner, J A; Bell-McGuinn, K M; Bhatia, J; Sabbatini, P; Aghajanian, C A; Offit, K; Barakat, R R; Spriggs, D R; Kauff, N D.
Afiliação
  • Gallagher DJ; Gynecologic Medical Oncology Service, Division of Solid Tumor Oncology, Department of Medicine; Clinical Genetics Service, Division of Solid Tumor Oncology, Department of Medicine.
  • Konner JA; Gynecologic Medical Oncology Service, Division of Solid Tumor Oncology, Department of Medicine.
  • Bell-McGuinn KM; Gynecologic Medical Oncology Service, Division of Solid Tumor Oncology, Department of Medicine.
  • Bhatia J; Clinical Genetics Service, Division of Solid Tumor Oncology, Department of Medicine.
  • Sabbatini P; Gynecologic Medical Oncology Service, Division of Solid Tumor Oncology, Department of Medicine.
  • Aghajanian CA; Gynecologic Medical Oncology Service, Division of Solid Tumor Oncology, Department of Medicine.
  • Offit K; Clinical Genetics Service, Division of Solid Tumor Oncology, Department of Medicine.
  • Barakat RR; Gynecology Service, Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, USA.
  • Spriggs DR; Gynecologic Medical Oncology Service, Division of Solid Tumor Oncology, Department of Medicine.
  • Kauff ND; Clinical Genetics Service, Division of Solid Tumor Oncology, Department of Medicine; Gynecology Service, Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, USA. Electronic address: kauffn@mskcc.org.
Ann Oncol ; 22(5): 1127-1132, 2011 May.
Article em En | MEDLINE | ID: mdl-21084428
ABSTRACT

BACKGROUND:

Patients with BRCA-associated ovarian cancer (OC) have a survival advantage over those with sporadic OC. To further explore this, we examined the impact of prognostic factors on disease-free survival (DFS) and overall survival (OS) in patients with known BRCA mutation status. PATIENTS AND

METHODS:

We reviewed stage III-IV OC patients treated at our institution between 1 December 1996 and 30 September 2006 and also tested on protocol for BRCA mutations. Impact on DFS and OS was determined by Kaplan-Meier analysis and a Cox proportional hazards model.

RESULTS:

Of the 110 patients, 36 had deleterious BRCA mutations [BRCA (+)] and 74 were BRCA wild type [BRCA(-)]. Thirty-one of 36 (86%) BRCA (+) and 60 of 74 (81%) BRCA (-) patients were platinum sensitive (P = 0.60). Median OS was longer for BRCA (+) patients (not reached versus 67.8 months; P = 0.02), but DFS was similar (26.9 versus 24.0, P = 0.3). On multivariate analysis, OS correlated with primary platinum sensitivity [HR = 0.15; 95% CI (confidence interval) 0.06-0.34] and BRCA (+) mutation status (HR = 0.33; 95% CI 0.12-0.86).

CONCLUSIONS:

BRCA mutation status predicted OS independent of primary platinum sensitivity, suggesting that underlying tumor biology contributes to disease outcome and may be worthy of consideration in future clinical trial design.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Platina / Proteína BRCA1 / Proteína BRCA2 / Mutação INDEL / Estudos de Associação Genética / Antineoplásicos Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies Limite: Female / Humans / Middle aged Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2011 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Platina / Proteína BRCA1 / Proteína BRCA2 / Mutação INDEL / Estudos de Associação Genética / Antineoplásicos Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies Limite: Female / Humans / Middle aged Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2011 Tipo de documento: Article