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Germline mutation in BRCA1 or BRCA2 and ten-year survival for women diagnosed with epithelial ovarian cancer.
Candido-dos-Reis, Francisco J; Song, Honglin; Goode, Ellen L; Cunningham, Julie M; Fridley, Brooke L; Larson, Melissa C; Alsop, Kathryn; Dicks, Ed; Harrington, Patricia; Ramus, Susan J; de Fazio, Anna; Mitchell, Gillian; Fereday, Sian; Bolton, Kelly L; Gourley, Charlie; Michie, Caroline; Karlan, Beth; Lester, Jenny; Walsh, Christine; Cass, Ilana; Olsson, Håkan; Gore, Martin; Benitez, Javier J; Garcia, Maria J; Andrulis, Irene; Mulligan, Anna Marie; Glendon, Gord; Blanco, Ignacio; Lazaro, Conxi; Whittemore, Alice S; McGuire, Valerie; Sieh, Weiva; Montagna, Marco; Alducci, Elisa; Sadetzki, Siegal; Chetrit, Angela; Kwong, Ava; Kjaer, Susanne K; Jensen, Allan; Høgdall, Estrid; Neuhausen, Susan; Nussbaum, Robert; Daly, Mary; Greene, Mark H; Mai, Phuong L; Loud, Jennifer T; Moysich, Kirsten; Toland, Amanda E; Lambrechts, Diether; Ellis, Steve.
Afiliação
  • Candido-dos-Reis FJ; Department of Gynecology and Obstetrics, Ribeirao Preto Medical School, University of Sao Paulo, Sao Paulo, Brazil.
  • Song H; Centre for Cancer Genetic Epidemiology, University of Cambridge, Cambridge, United Kingdom.
  • Goode EL; Mayo Clinic, Rochester, Minnesota.
  • Cunningham JM; Mayo Clinic, Rochester, Minnesota.
  • Fridley BL; University of Kansas Medical Center, Kansas City, Kansas.
  • Larson MC; Mayo Clinic, Rochester, Minnesota.
  • Alsop K; The Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
  • Dicks E; Centre for Cancer Genetic Epidemiology, University of Cambridge, Cambridge, United Kingdom.
  • Harrington P; Centre for Cancer Genetic Epidemiology, University of Cambridge, Cambridge, United Kingdom.
  • Ramus SJ; Department of Preventive Medicine, Keck School of Medicine, University of Southern California Norris Comprehensive Cancer Center, Los Angeles, California.
  • de Fazio A; Department of Gynaecological Oncology, Crown Princess Mary Cancer Centre and Westmead Institute for Cancer Research, University of Sydney at Westmead Millennium Institute, Westmead Hospital, Sydney NSW, Australia.
  • Mitchell G; The Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
  • Fereday S; The Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
  • Bolton KL; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.
  • Gourley C; University of Edinburgh Cancer Research UK Centre, MRC IGMM, Edinburgh, United Kingdom.
  • Michie C; Ninewells Hospital and Medical School, Dundee, United Kingdom.
  • Karlan B; Women's Cancer Program at the Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California.
  • Lester J; Women's Cancer Program at the Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California.
  • Walsh C; Women's Cancer Program at the Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California.
  • Cass I; Women's Cancer Program at the Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California.
  • Olsson H; Departments of Cancer Epidemiology and Oncology, Lund University, Lund, Sweden.
  • Gore M; Royal Marsden NHS Foundation Trust, London, United Kingdom.
  • Benitez JJ; Human Genetics Group and Human Genotyping Unit Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
  • Garcia MJ; Human Genetics Group and Human Genotyping Unit Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
  • Andrulis I; Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital; Departments of Molecular Genetics and Laboratory Medicine and Pathobiology, University of Toronto, Ontario, Canada.
  • Mulligan AM; Laboratory Medicine Program, University Health Network; Department of Laboratory Medicine and Pathobiology, University of Toronto, Ontario, Canada.
  • Glendon G; Laboratory Medicine Program, University Health Network; Department of Laboratory Medicine and Pathobiology, University of Toronto, Ontario, Canada.
  • Blanco I; Hereditary Cancer Program, Catalan Institute of Oncology, L'Hospitalet, Barcelona, Spain.
  • Lazaro C; Hereditary Cancer Program, Catalan Institute of Oncology, L'Hospitalet, Barcelona, Spain.
  • Whittemore AS; Department of Health Research and Policy-Epidemiology, Stanford University School of Medicine, Stanford, California.
  • McGuire V; Department of Health Research and Policy-Epidemiology, Stanford University School of Medicine, Stanford, California.
  • Sieh W; Department of Health Research and Policy-Epidemiology, Stanford University School of Medicine, Stanford, California.
  • Montagna M; Immunology and Molecular Oncology Unit, Istituto Oncologico Veneto IOV-IRCCS, Padua, Italy.
  • Alducci E; Immunology and Molecular Oncology Unit, Istituto Oncologico Veneto IOV-IRCCS, Padua, Italy.
  • Sadetzki S; Gertner Institute for Epidemiology and Health Policy Research, Sheba Medical Center, Tel Hashomer, Israel.
  • Chetrit A; Gertner Institute for Epidemiology and Health Policy Research, Sheba Medical Center, Tel Hashomer, Israel.
  • Kwong A; The Hong Kong Hereditary Breast Cancer Family Registry, Cancer Genetics Center, Hong Kong, Hong Kong.
  • Kjaer SK; Department of Virus, Lifestyle and Genes, Danish Cancer Society Research Center, Copenhagen, Denmark.
  • Jensen A; Department of Virus, Lifestyle and Genes, Danish Cancer Society Research Center, Copenhagen, Denmark.
  • Høgdall E; Molecular Unit, Department of Pathology, Herlev Hospital, University of Copenhagen, Copenhagen, Denmark.
  • Neuhausen S; Department of Population Sciences, Beckman Research Institute of the City of Hope, Duarte, California.
  • Nussbaum R; University of California San Francisco, Cancer Risk Program, San Francisco, California.
  • Daly M; Department of Clinical Genetics, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
  • Greene MH; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.
  • Mai PL; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.
  • Loud JT; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.
  • Moysich K; Department of Cancer Prevention and Control, Roswell Park Cancer Institute, Buffalo, New York.
  • Toland AE; Departments of Internal Medicine and Molecular Virology, Immunology, and Medical Genetics, The Comprehensive Cancer Center, Ohio State University, Columbus, Ohio.
  • Lambrechts D; VIB Vesalius Research Center, University of Leuven, Leuven, Belgium.
  • Ellis S; Centre for Cancer Genetic Epidemiology, University of Cambridge, Cambridge, United Kingdom.
Clin Cancer Res ; 21(3): 652-7, 2015 Feb 01.
Article em En | MEDLINE | ID: mdl-25398451
PURPOSE: To analyze the effect of germline mutations in BRCA1 and BRCA2 on mortality in patients with ovarian cancer up to 10 years after diagnosis. EXPERIMENTAL DESIGN: We used unpublished survival time data for 2,242 patients from two case-control studies and extended survival time data for 4,314 patients from previously reported studies. All participants had been screened for deleterious germline mutations in BRCA1 and BRCA2. Survival time was analyzed for the combined data using Cox proportional hazard models with BRCA1 and BRCA2 as time-varying covariates. Competing risks were analyzed using Fine and Gray model. RESULTS: The combined 10-year overall survival rate was 30% [95% confidence interval (CI), 28%-31%] for non-carriers, 25% (95% CI, 22%-28%) for BRCA1 carriers, and 35% (95% CI, 30%-41%) for BRCA2 carriers. The HR for BRCA1 was 0.53 at time zero and increased over time becoming greater than one at 4.8 years. For BRCA2, the HR was 0.42 at time zero and increased over time (predicted to become greater than 1 at 10.5 years). The results were similar when restricted to 3,202 patients with high-grade serous tumors and to ovarian cancer-specific mortality. CONCLUSIONS: BRCA1/2 mutations are associated with better short-term survival, but this advantage decreases over time and in BRCA1 carriers is eventually reversed. This may have important implications for therapy of both primary and relapsed disease and for analysis of long-term survival in clinical trials of new agents, particularly those that are effective in BRCA1/2 mutation carriers.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Mutação em Linhagem Germinativa / Neoplasias Epiteliais e Glandulares / Genes BRCA1 / Genes BRCA2 Idioma: En Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Mutação em Linhagem Germinativa / Neoplasias Epiteliais e Glandulares / Genes BRCA1 / Genes BRCA2 Idioma: En Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Brasil