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PMID: 26857456 已发表 · epublish 英语

Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2.

Breast cancer research : BCR ·第 18 卷 ·第 1 期 ·2016-10-05

Silvestri Valentina, Barrowdale Daniel, Mulligan Anna Marie, Neuhausen Susan L, Fox Stephen, Karlan Beth Y, Mitchell Gillian, James Paul, Thull Darcy L, Zorn Kristin K, Carter Natalie J, Nathanson Katherine L, Domchek Susan M, Rebbeck Timothy R, Ramus Susan J, Nussbaum Robert L, Olopade Olufunmilayo I, Rantala Johanna, Yoon Sook-Yee, Caligo Maria A, Spugnesi Laura, Bojesen Anders, Pedersen Inge Sokilde, Thomassen Mads, Jensen Uffe Birk, Toland Amanda Ewart, Senter Leigha, Andrulis Irene L, Glendon Gord, Hulick Peter J, Imyanitov Evgeny N, Greene Mark H, Mai Phuong L, Singer Christian F, Rappaport-Fuerhauser Christine, Kramer Gero, Vijai Joseph, Offit Kenneth, Robson Mark, Lincoln Anne, Jacobs Lauren, Machackova Eva, Foretova Lenka, Navratilova Marie, Vasickova Petra, Couch Fergus J, Hallberg Emily, Ruddy Kathryn J, Sharma Priyanka, Kim Sung-Won, , Teixeira Manuel R, Pinto Pedro, Montagna Marco, Matricardi Laura, Arason Adalgeir, Johannsson Oskar Th, Barkardottir Rosa B, Jakubowska Anna, Lubinski Jan, Izquierdo Angel, Pujana Miguel Angel, Balmaña Judith, Diez Orland, Ivady Gabriella, Papp Janos, Olah Edith, Kwong Ava, , Nevanlinna Heli, Aittomäki Kristiina, Perez Segura Pedro, Caldes Trinidad, Van Maerken Tom, Poppe Bruce, Claes Kathleen B M, Isaacs Claudine, Elan Camille, Lasset Christine, Stoppa-Lyonnet Dominique, Barjhoux Laure, Belotti Muriel, Meindl Alfons, Gehrig Andrea, Sutter Christian, Engel Christoph, Niederacher Dieter, Steinemann Doris, Hahnen Eric, Kast Karin, Arnold Norbert, Varon-Mateeva Raymonda, Wand Dorothea, Godwin Andrew K, Evans D Gareth, Frost Debra, Perkins Jo, Adlard Julian, Izatt Louise, Platte Radka, Eeles Ros, Ellis Steve, , Hamann Ute, Garber Judy, Fostira Florentia, Fountzilas George, Pasini Barbara, Giannini Giuseppe, Rizzolo Piera, Russo Antonio, Cortesi Laura, Papi Laura, Varesco Liliana, Palli Domenico, Zanna Ines, Savarese Antonella, Radice Paolo, Manoukian Siranoush, Peissel Bernard, Barile Monica, Bonanni Bernardo, Viel Alessandra, Pensotti Valeria, Tommasi Stefania, Peterlongo Paolo, Weitzel Jeffrey N, Osorio Ana, Benitez Javier, McGuffog Lesley, Healey Sue, Gerdes Anne-Marie, Ejlertsen Bent, Hansen Thomas V O, Steele Linda, Ding Yuan Chun, Tung Nadine, Janavicius Ramunas, Goldgar David E, Buys Saundra S, Daly Mary B, Bane Anita, Terry Mary Beth, John Esther M, Southey Melissa, Easton Douglas F, Chenevix-Trench Georgia, Antoniou Antonis C, Ottini Laura

摘要

BRCA1 and, more commonly, BRCA2 mutations are associated with increased risk of male breast cancer (MBC). However, only a paucity of data exists on the pathology of breast cancers (BCs) in men with BRCA1/2 mutations. Using the largest available dataset, we determined whether MBCs arising in BRCA1/2 mutation carriers display specific pathologic features and whether these features differ from those of BRCA1/2 female BCs (FBCs).,We characterised the pathologic features of 419 BRCA1/2 MBCs and, using logistic regression analysis, contrasted those with data from 9675 BRCA1/2 FBCs and with population-based data from 6351 MBCs in the Surveillance, Epidemiology, and End Results (SEER) database.,Among BRCA2 MBCs, grade significantly decreased with increasing age at diagnosis (P = 0.005). Compared with BRCA2 FBCs, BRCA2 MBCs were of significantly higher stage (P for trend = 2 × 10(-5)) and higher grade (P for trend = 0.005) and were more likely to be oestrogen receptor-positive [odds ratio (OR) 10.59; 95 % confidence interval (CI) 5.15-21.80] and progesterone receptor-positive (OR 5.04; 95 % CI 3.17-8.04). With the exception of grade, similar patterns of associations emerged when we compared BRCA1 MBCs and FBCs. BRCA2 MBCs also presented with higher grade than MBCs from the SEER database (P for trend = 4 × 10(-12)).,On the basis of the largest series analysed to date, our results show that BRCA1/2 MBCs display distinct pathologic characteristics compared with BRCA1/2 FBCs, and we identified a specific BRCA2-associated MBC phenotype characterised by a variable suggesting greater biological aggressiveness (i.e., high histologic grade). These findings could lead to the development of gender-specific risk prediction models and guide clinical strategies appropriate for MBC management.

文献信息
期刊
Breast cancer research : BCR
期刊简称
Breast Cancer Res
发表日期
2016-10-05
收录日期
2016-02-09
更新日期
2016-12-03
语言
英语
国家/地区
England
NLM ID
100927353
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