<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7</volume><submitter>Humphries MP</submitter><pubmed_abstract>Male breast cancer (MBC) is rare. We assembled 446 MBCs on tissue microarrays and assessed clinicopathological information, together with data from 15 published studies, totalling 1984 cases. By immunohistochemistry we investigated 14 biomarkers (ERα, ERβ1, ERβ2, ERβ5, PR, AR, Bcl-2, HER2, p53, E-cadherin, Ki67, survivin, prolactin, FOXA1) for survival impact. The main histological subtype in our cohort and combined analyses was ductal (81%, 83%), grade 2; (40%, 44%), respectively. Cases were predominantly ERα (84%, 82%) and PR positive (74%, 71%), respectively, with HER2 expression being infrequent (2%, 10%), respectively. In our cohort, advanced age (>67) was the strongest predictor of overall (OS) and disease free survival (DFS) (p = 0.00001; p = 0.01, respectively). Node positivity neg</pubmed_abstract><journal>Scientific reports</journal><pagination>45293</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5368596</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Characterisation of male breast cancer: a descriptive biomarker study from a large patient series.</pubmed_title><pmcid>PMC5368596</pmcid><pubmed_authors>Hanby AM</pubmed_authors><pubmed_authors>Provenzano E</pubmed_authors><pubmed_authors>Fulford L</pubmed_authors><pubmed_authors>Humphries MP</pubmed_authors><pubmed_authors>Stephens M</pubmed_authors><pubmed_authors>Jones JL</pubmed_authors><pubmed_authors>Titloye AN</pubmed_authors><pubmed_authors>Speirs V</pubmed_authors><pubmed_authors>Jordan LB</pubmed_authors><pubmed_authors>Kanthan R</pubmed_authors><pubmed_authors>Shousha S</pubmed_authors><pubmed_authors>Ellis IO</pubmed_authors><pubmed_authors>Cserni G</pubmed_authors><pubmed_authors>Di Benedetto A</pubmed_authors><pubmed_authors>Litwiniuk M</pubmed_authors><pubmed_authors>Mottolese M</pubmed_authors><pubmed_authors>Sundara Rajan S</pubmed_authors><pubmed_authors>Honarpisheh H</pubmed_authors><pubmed_authors>Kulka J</pubmed_authors><pubmed_authors>Dent J</pubmed_authors><pubmed_authors>Shaaban AM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Characterisation of male breast cancer: a descriptive biomarker study from a large patient series.</name><description>Male breast cancer (MBC) is rare. We assembled 446 MBCs on tissue microarrays and assessed clinicopathological information, together with data from 15 published studies, totalling 1984 cases. By immunohistochemistry we investigated 14 biomarkers (ERα, ERβ1, ERβ2, ERβ5, PR, AR, Bcl-2, HER2, p53, E-cadherin, Ki67, survivin, prolactin, FOXA1) for survival impact. The main histological subtype in our cohort and combined analyses was ductal (81%, 83%), grade 2; (40%, 44%), respectively. Cases were predominantly ERα (84%, 82%) and PR positive (74%, 71%), respectively, with HER2 expression being infrequent (2%, 10%), respectively. In our cohort, advanced age (>67) was the strongest predictor of overall (OS) and disease free survival (DFS) (p = 0.00001; p = 0.01, respectively). Node positivity neg</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Mar</publication><modification>2025-04-04T18:45:23.566Z</modification><creation>2019-03-27T02:39:41Z</creation></dates><accession>S-EPMC5368596</accession><cross_references><pubmed>28350011</pubmed><doi>10.1038/srep45293</doi></cross_references></HashMap>