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Characterization of male breast cancer: results of the EORTC 10085/TBCRC/BIG/NABCG International Male Breast Cancer Program.
Cardoso, F; Bartlett, J M S; Slaets, L; van Deurzen, C H M; van Leeuwen-Stok, E; Porter, P; Linderholm, B; Hedenfalk, I; Schröder, C; Martens, J; Bayani, J; van Asperen, C; Murray, M; Hudis, C; Middleton, L; Vermeij, J; Punie, K; Fraser, J; Nowaczyk, M; Rubio, I T; Aebi, S; Kelly, C; Ruddy, K J; Winer, E; Nilsson, C; Lago, L Dal; Korde, L; Benstead, K; Bogler, O; Goulioti, T; Peric, A; Litière, S; Aalders, K C; Poncet, C; Tryfonidis, K; Giordano, S H.
Afiliación
  • Cardoso F; Breast Unit, Champalimaud Clinical Center/Champalimaud Foundation, Lisbon, Portugal; European Organisation for Research and Treatment of Cancer-Breast Cancer Group, Toronto, Canada. Electronic address: fatimacardoso@fundacaochampalimaud.pt.
  • Bartlett JMS; Transformative Pathology, Ontario Institute for Cancer Research, Toronto, Canada; University of Edinburgh, Edinburgh, UK.
  • Slaets L; European Organization for Research and Treatment of Cancer (EORTC) Headquarters, Brussels, Belgium.
  • van Deurzen CHM; Department of Pathology, Erasmus Medical Center, Rotterdam, The Netherlands; Dutch Breast Cancer Research Group (BOOG), The Netherlands.
  • van Leeuwen-Stok E; Dutch Breast Cancer Research Group (BOOG), The Netherlands.
  • Porter P; Divisions of Human Biology and Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, USA; Department of Pathology, University of Washington, Seattle, USA.
  • Linderholm B; Department of Oncology, Sahlgrenska University Hospital, Gothenburg, Sweden; Swedish Association of Breast Oncologists (SABO), Lund University, Lund, Sweden.
  • Hedenfalk I; Division of Oncology and Pathology, Department of Clinical Sciences, Lund University, Lund, Sweden.
  • Schröder C; Dutch Breast Cancer Research Group (BOOG), The Netherlands; Department of Medical Oncology, University Medical Center Groningen, Groningen, The Netherlands.
  • Martens J; Dutch Breast Cancer Research Group (BOOG), The Netherlands; Breast Cancer Genomics and Proteomics Lab, Erasmus Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Bayani J; Transformative Pathology, Ontario Institute for Cancer Research, Toronto, Canada.
  • van Asperen C; Dutch Breast Cancer Research Group (BOOG), The Netherlands; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Murray M; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York.
  • Hudis C; Breast Medicine Service, Memorial Sloan Kettering Cancer Center, New York; Weill Cornell Medical College, New York.
  • Middleton L; Department of Pathology, University of Texas MD Anderson Cancer Center, Houston, USA.
  • Vermeij J; Department of Medical Oncology, Hospital Network Antwerp (ZNA), Antwerp, Belgium.
  • Punie K; Department of General Medical Oncology, UZ Leuven, Leuven, Belgium.
  • Fraser J; Beatson West of Scotland Cancer Centre, Glasgow, UK.
  • Nowaczyk M; Specialist Hospital, St. Wojciech, Gdansk, Poland.
  • Rubio IT; Breast Surgical Unit, Hospital Universitario Vall d'Hebron, Barcelona, Spain.
  • Aebi S; Swiss Group for Clinical Cancer Research (SAKK), Switzerland.
  • Kelly C; All Ireland Cooperative Oncology Research Group (ICORG), Ireland.
  • Ruddy KJ; Department of Oncology, Mayo Clinic, Rochester, USA.
  • Winer E; Dana-Farber Cancer Institute, Boston, USA.
  • Nilsson C; Department of Oncology, Västmanlands Hospital, Västerås, Sweden; Swedish Association of Breast Oncologists (SABO), Sweden.
  • Lago LD; Department of Medical Oncology, Jules Bordet Institute, Brussels, Belgium.
  • Korde L; University of Washington, Seattle, USA.
  • Benstead K; Department of Oncology, Cheltenham General Hospital, UK.
  • Bogler O; Global Academic Programs, University of Texas MD Anderson Cancer Center, Houston, USA.
  • Goulioti T; Breast International Group, Brussels, Belgium.
  • Peric A; European Organization for Research and Treatment of Cancer (EORTC) Headquarters, Brussels, Belgium.
  • Litière S; European Organization for Research and Treatment of Cancer (EORTC) Headquarters, Brussels, Belgium.
  • Aalders KC; European Organization for Research and Treatment of Cancer (EORTC) Headquarters, Brussels, Belgium.
  • Poncet C; European Organization for Research and Treatment of Cancer (EORTC) Headquarters, Brussels, Belgium.
  • Tryfonidis K; European Organization for Research and Treatment of Cancer (EORTC) Headquarters, Brussels, Belgium.
  • Giordano SH; Departments of Health Services Research and Breast Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, USA.
Ann Oncol ; 29(2): 405-417, 2018 02 01.
Article en En | MEDLINE | ID: mdl-29092024
ABSTRACT

Background:

Male breast cancer (BC) is rare, managed by extrapolation from female BC. The International Male BC Program aims to better characterize and manage this disease. We report the results of part I, a retrospective joint analysis of cases diagnosed during a 20-year period.

Methods:

Patients with follow-up and tumor samples, treated between 1990 and 2010, in 93 centers/9 countries. Samples were centrally analyzed in three laboratories (the United Kingdom, the Netherlands and the United States).

Results:

Of 1822 patients enrolled, 1483 were analyzed; 63.5% were diagnosed between 2001 and 2010, 57 (5.1%) had metastatic disease (M1). Median age at diagnosis 68.4 years. Of 1054 M0 cases, 56.2% were node-negative (N0) and 48.5% had T1 tumors; 4% had breast conserving surgery (BCS), 18% sentinel lymph-node biopsy; half received adjuvant radiotherapy; 29.8% (neo)adjuvant chemotherapy and 76.8% adjuvant endocrine therapy (ET), mostly tamoxifen (88.4%). Per central pathology, for M0 tumors 84.8% ductal invasive carcinomas, 51.5% grade 2; 99.3% estrogen receptor (ER)-positive; 81.9% progesterone receptor (PR)-positive; 96.9% androgen receptor (AR)-positive [ER, PR or AR Allred score ≥3]; 61.1% Ki67 expression low (<14% positive cells); using immunohistochemistry (IHC) surrogates, 41.9% were Luminal-A-like, 48.6% Luminal-B-like/HER-2-negative, 8.7% HER-2-positive, 0.3% triple negative. Median follow-up 8.2 years (0.0-23.8) for all, 7.2 years (0.0-23.2), for M0, 2.6 years (0.0-12.7) for M1 patients. A significant improvement over time was observed in age-corrected BC mortality. BC-specific-mortality was higher for men younger than 50 years. Better overall (OS) and recurrence-free survival (RFS) were observed for highly ER+ (P = 0.001), highly PR+ (P = 0.002), highly AR+ disease (P = 0.019). There was no association between OS/RFS and HER-2 status, Ki67, IHC subtypes nor grade.

Conclusions:

Male BC is usually ER, PR and AR-positive, Luminal B-like/HER2-negative. Of note, 56% patients had T1 tumors but only 4% had BCS. ER was highly positive in >90% of cases but only 77% received adjuvant ET. ER, PR and AR were associated with OS and RFS, whereas grade, Ki67 and IHC surrogates were not. Significant improvement in survival over time was observed.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias de la Mama Masculina Tipo de estudio: Observational_studies / Prognostic_studies Límite: Adult / Aged / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Asunto de la revista: NEOPLASIAS Año: 2018 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias de la Mama Masculina Tipo de estudio: Observational_studies / Prognostic_studies Límite: Adult / Aged / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Asunto de la revista: NEOPLASIAS Año: 2018 Tipo del documento: Article