Evaluation of multiple transcriptomic gene risk signatures in male breast cancer

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作者
Jane Bayani
Coralie Poncet
Cheryl Crozier
Anouk Neven
Tammy Piper
Carrie Cunningham
Monika Sobol
Stefan Aebi
Kim Benstead
Oliver Bogler
Lissandra Dal Lago
Judith Fraser
Florentine Hilbers
Ingrid Hedenfalk
Larissa Korde
Barbro Linderholm
John Martens
Lavinia Middleton
Melissa Murray
Catherine Kelly
Cecilia Nilsson
Monika Nowaczyk
Stephanie Peeters
Aleksandra Peric
Peggy Porter
Carolien Schröder
Isabel T. Rubio
Kathryn J. Ruddy
Christi van Asperen
Danielle Van Den Weyngaert
Carolien van Deurzen
Elise van Leeuwen-Stok
Joanna Vermeij
Eric Winer
Sharon H. Giordano
Fatima Cardoso
John M. S. Bartlett
机构
[1] Ontario Institute for Cancer Research,Department of Statistics
[2] Department of Laboratory Medicine and Pathobiology,Department of Oncology
[3] University of Toronto,Global Academic Programs
[4] European Organization for Research and Treatment of Cancer (EORTC) Headquarters,Department of Medical Oncology
[5] University of Edinburgh,Division of Oncology, Department of Clinical Sciences
[6] Swiss Group for Clinical Cancer Research (SAKK),Department of Oncology
[7] Cheltenham General Hospital,Department Pathology
[8] University of Texas MD Anderson Cancer Center,Department of Pathology
[9] Jules Bordet Institute,Department of Oncology
[10] Beatson West of Scotland Cancer Centre,Divisions of Human Biology and Public Health Sciences, Fred Hutchinson Cancer Research Center & Department of Pathology
[11] Breast International Group,Department Medical Oncology
[12] Lund University,Department of Clinical Genetics
[13] University of Washington,Department of Radiotherapy
[14] Sahlgrenska University Hospital,Department Pathology
[15] Medical Oncology,Department of Medical Oncology
[16] Erasmus Medical Center Rotterdam; BOOG,undefined
[17] University of Texas MD Anderson Cancer Center,undefined
[18] Memorial Sloan Kettering Cancer Center,undefined
[19] All Ireland Cooperative Oncology Research Group (ICORG),undefined
[20] Västmanlands Hospital,undefined
[21] Specialist Hospital. St. Wojciech,undefined
[22] Department of Radiation Oncology Maastro,undefined
[23] University of Washington,undefined
[24] University Medical Center Groningen; BOOG,undefined
[25] Breast Surgical Unit. Hospital Universitario Vall d´Hebron,undefined
[26] Mayo Clinic,undefined
[27] Department of Oncology,undefined
[28] Leiden University Medical Center; BOOG,undefined
[29] ZNA Middelheim,undefined
[30] Erasmus Medical Center; BOOG,undefined
[31] Dutch Breast Cancer Research Group (BOOG),undefined
[32] ZNA Jan Palfijn,undefined
[33] Dana-Farber Cancer Institute,undefined
[34] University of Texas MD Anderson Cancer Center,undefined
[35] Breast Unit,undefined
[36] Champalimaud Clinical Center/Champalimaud Foundation; EORTC,undefined
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摘要
Male breast cancer (BCa) is a rare disease accounting for less than 1% of all breast cancers and 1% of all cancers in males. The clinical management is largely extrapolated from female BCa. Several multigene assays are increasingly used to guide clinical treatment decisions in female BCa, however, there are limited data on the utility of these tests in male BCa. Here we present the gene expression results of 381 M0, ER+ve, HER2-ve male BCa patients enrolled in the Part 1 (retrospective analysis) of the International Male Breast Cancer Program. Using a custom NanoString™ panel comprised of the genes from the commercial risk tests Prosigna®, OncotypeDX®, and MammaPrint®, risk scores and intrinsic subtyping data were generated to recapitulate the commercial tests as described by us previously. We also examined the prognostic value of other risk scores such as the Genomic Grade Index (GGI), IHC4-mRNA and our prognostic 95-gene signature. In this sample set of male BCa, we demonstrated prognostic utility on univariate analysis. Across all signatures, patients whose samples were identified as low-risk experienced better outcomes than intermediate-risk, with those classed as high risk experiencing the poorest outcomes. As seen with female BCa, the concordance between tests was poor, with C-index values ranging from 40.3% to 78.2% and Kappa values ranging from 0.17 to 0.58. To our knowledge, this is the largest study of male breast cancers assayed to generate risk scores of the current commercial and academic risk tests demonstrating comparable clinical utility to female BCa.
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