Cargando…

Evaluation of multiple transcriptomic gene risk signatures in male breast cancer

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, t...

Descripción completa

Detalles Bibliográficos
Autores principales: Bayani, Jane, Poncet, Coralie, Crozier, Cheryl, Neven, Anouk, Piper, Tammy, Cunningham, Carrie, Sobol, Monika, Aebi, Stefan, Benstead, Kim, Bogler, Oliver, Dal Lago, Lissandra, Fraser, Judith, Hilbers, Florentine, Hedenfalk, Ingrid, Korde, Larissa, Linderholm, Barbro, Martens, John, Middleton, Lavinia, Murray, Melissa, Kelly, Catherine, Nilsson, Cecilia, Nowaczyk, Monika, Peeters, Stephanie, Peric, Aleksandra, Porter, Peggy, Schröder, Carolien, Rubio, Isabel T., Ruddy, Kathryn J., van Asperen, Christi, Van Den Weyngaert, Danielle, van Deurzen, Carolien, van Leeuwen-Stok, Elise, Vermeij, Joanna, Winer, Eric, Giordano, Sharon H., Cardoso, Fatima, Bartlett, John M. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8313692/
https://www.ncbi.nlm.nih.gov/pubmed/34312396
http://dx.doi.org/10.1038/s41523-021-00301-0
_version_ 1783729396186611712
author Bayani, Jane
Poncet, Coralie
Crozier, Cheryl
Neven, Anouk
Piper, Tammy
Cunningham, Carrie
Sobol, Monika
Aebi, Stefan
Benstead, Kim
Bogler, Oliver
Dal Lago, Lissandra
Fraser, Judith
Hilbers, Florentine
Hedenfalk, Ingrid
Korde, Larissa
Linderholm, Barbro
Martens, John
Middleton, Lavinia
Murray, Melissa
Kelly, Catherine
Nilsson, Cecilia
Nowaczyk, Monika
Peeters, Stephanie
Peric, Aleksandra
Porter, Peggy
Schröder, Carolien
Rubio, Isabel T.
Ruddy, Kathryn J.
van Asperen, Christi
Van Den Weyngaert, Danielle
van Deurzen, Carolien
van Leeuwen-Stok, Elise
Vermeij, Joanna
Winer, Eric
Giordano, Sharon H.
Cardoso, Fatima
Bartlett, John M. S.
author_facet Bayani, Jane
Poncet, Coralie
Crozier, Cheryl
Neven, Anouk
Piper, Tammy
Cunningham, Carrie
Sobol, Monika
Aebi, Stefan
Benstead, Kim
Bogler, Oliver
Dal Lago, Lissandra
Fraser, Judith
Hilbers, Florentine
Hedenfalk, Ingrid
Korde, Larissa
Linderholm, Barbro
Martens, John
Middleton, Lavinia
Murray, Melissa
Kelly, Catherine
Nilsson, Cecilia
Nowaczyk, Monika
Peeters, Stephanie
Peric, Aleksandra
Porter, Peggy
Schröder, Carolien
Rubio, Isabel T.
Ruddy, Kathryn J.
van Asperen, Christi
Van Den Weyngaert, Danielle
van Deurzen, Carolien
van Leeuwen-Stok, Elise
Vermeij, Joanna
Winer, Eric
Giordano, Sharon H.
Cardoso, Fatima
Bartlett, John M. S.
author_sort Bayani, Jane
collection PubMed
description 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.
format Online
Article
Text
id pubmed-8313692
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-83136922021-08-02 Evaluation of multiple transcriptomic gene risk signatures in male breast cancer Bayani, Jane Poncet, Coralie Crozier, Cheryl Neven, Anouk Piper, Tammy Cunningham, Carrie Sobol, Monika Aebi, Stefan Benstead, Kim Bogler, Oliver Dal Lago, Lissandra Fraser, Judith Hilbers, Florentine Hedenfalk, Ingrid Korde, Larissa Linderholm, Barbro Martens, John Middleton, Lavinia Murray, Melissa Kelly, Catherine Nilsson, Cecilia Nowaczyk, Monika Peeters, Stephanie Peric, Aleksandra Porter, Peggy Schröder, Carolien Rubio, Isabel T. Ruddy, Kathryn J. van Asperen, Christi Van Den Weyngaert, Danielle van Deurzen, Carolien van Leeuwen-Stok, Elise Vermeij, Joanna Winer, Eric Giordano, Sharon H. Cardoso, Fatima Bartlett, John M. S. NPJ Breast Cancer Article 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. Nature Publishing Group UK 2021-07-26 /pmc/articles/PMC8313692/ /pubmed/34312396 http://dx.doi.org/10.1038/s41523-021-00301-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bayani, Jane
Poncet, Coralie
Crozier, Cheryl
Neven, Anouk
Piper, Tammy
Cunningham, Carrie
Sobol, Monika
Aebi, Stefan
Benstead, Kim
Bogler, Oliver
Dal Lago, Lissandra
Fraser, Judith
Hilbers, Florentine
Hedenfalk, Ingrid
Korde, Larissa
Linderholm, Barbro
Martens, John
Middleton, Lavinia
Murray, Melissa
Kelly, Catherine
Nilsson, Cecilia
Nowaczyk, Monika
Peeters, Stephanie
Peric, Aleksandra
Porter, Peggy
Schröder, Carolien
Rubio, Isabel T.
Ruddy, Kathryn J.
van Asperen, Christi
Van Den Weyngaert, Danielle
van Deurzen, Carolien
van Leeuwen-Stok, Elise
Vermeij, Joanna
Winer, Eric
Giordano, Sharon H.
Cardoso, Fatima
Bartlett, John M. S.
Evaluation of multiple transcriptomic gene risk signatures in male breast cancer
title Evaluation of multiple transcriptomic gene risk signatures in male breast cancer
title_full Evaluation of multiple transcriptomic gene risk signatures in male breast cancer
title_fullStr Evaluation of multiple transcriptomic gene risk signatures in male breast cancer
title_full_unstemmed Evaluation of multiple transcriptomic gene risk signatures in male breast cancer
title_short Evaluation of multiple transcriptomic gene risk signatures in male breast cancer
title_sort evaluation of multiple transcriptomic gene risk signatures in male breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8313692/
https://www.ncbi.nlm.nih.gov/pubmed/34312396
http://dx.doi.org/10.1038/s41523-021-00301-0
work_keys_str_mv AT bayanijane evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT poncetcoralie evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT croziercheryl evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT nevenanouk evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT pipertammy evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT cunninghamcarrie evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT sobolmonika evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT aebistefan evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT bensteadkim evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT bogleroliver evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT dallagolissandra evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT fraserjudith evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT hilbersflorentine evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT hedenfalkingrid evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT kordelarissa evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT linderholmbarbro evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT martensjohn evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT middletonlavinia evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT murraymelissa evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT kellycatherine evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT nilssoncecilia evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT nowaczykmonika evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT peetersstephanie evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT pericaleksandra evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT porterpeggy evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT schrodercarolien evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT rubioisabelt evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT ruddykathrynj evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT vanasperenchristi evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT vandenweyngaertdanielle evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT vandeurzencarolien evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT vanleeuwenstokelise evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT vermeijjoanna evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT winereric evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT giordanosharonh evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT cardosofatima evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer
AT bartlettjohnms evaluationofmultipletranscriptomicgenerisksignaturesinmalebreastcancer