Prediction of BRCA1 status in patients with breast cancer using estrogen receptor and basal phenotype

被引:474
作者
Lakhani, SR
Reis-Filho, JS
Fulford, L
Penault-Llorca, F
van der Vjiver, M
Parry, S
Bishop, T
Benitez, J
Rivas, C
Bignon, YJ
Chang-Claude, J
Hamann, U
Cornelisse, CJ
Devilee, P
Beckmann, MW
Nestle-Krämling, C
Daly, PA
Haites, N
Varley, J
Lalloo, F
Evans, G
Maugard, C
Meijers-Heijboer, H
Klijn, JGM
Olah, E
Gusterson, BA
Pilotti, S
Radice, P
Scherneck, S
Sobol, H
Jacquemier, J
Wagner, T
Peto, J
Stratton, MR
McGuffog, L
Easton, DF
机构
[1] Univ Queensland, Mayne Med Sch, Brisbane, Qld 4006, Australia
[2] Inst Canc Res, Breakthrough Toby Robins Breast Canc Res Ctr, London, England
[3] Canc Res UK, Genet Epidemiol Unit, Cambridge, England
[4] Ctr Jean Perrin, Clermont Ferrand, France
[5] Netherlands Canc Inst, Amsterdam, Netherlands
[6] St James Univ Hosp, Imperial Canc Res Fund Genet Epidemiol Lab, Leeds, W Yorkshire, England
[7] Ctr Nacl Invest Oncol, Dpto Genet Humana, Dept Genet, Madrid, Spain
[8] Univ Autonoma Madrid, Dept Pathol, Fundac Jimenez Diaz, Madrid, Spain
[9] Deutsch Krebsforschungszentrum, Div Epidemiol & Mol, Heidelberg, Germany
[10] Deutsch Krebsforschungszentrum, Dept Genome Anal, Heidelberg, Germany
[11] Leiden Univ, Dept Genet & Pathol, Leiden, Netherlands
[12] Univ Erlangen Nurnberg, Dept Obstet, Erlangen, Germany
[13] Univ Erlangen Nurnberg, Dept Gynecol, Erlangen, Germany
[14] St James Hosp, Trinity Coll, Sch Med, Dept Med, Dublin, Ireland
[15] Univ Aberdeen, Dept Med & Therapeut, Aberdeen, Scotland
[16] Peterson Inst Canc Res, CRUK Canc Genet Grp, Manchester, Lancs, England
[17] St Marys Hosp, Dept Med Genet, Manchester, Lancs, England
[18] Univ Hosp, Nantes, France
[19] Erasmus Univ, Med Ctr, Daniel Hoed Canc Ctr, Dept Clin Genet & Med Oncol, Rotterdam, Netherlands
[20] Natl Inst Oncol, Dept Biol Mol, Budapest, Hungary
[21] Univ Glasgow, Western Infirm, Dept Pathol, Glasgow, Lanark, Scotland
[22] Ist Nazl Tumori, Dept Expt Oncol, Milan, Italy
[23] Ist Nazl Tumori, Dept Pathol, Milan, Italy
[24] Max Delbruck Centrum Mol Med, Berlin, Germany
[25] Inst Natl Sante & Rech Med, Dept Genet Oncol & Canc Control, Marseille, France
[26] Univ Vienna, Gen Hosp, Dept Obstet & Gynaecol, Vienna, Austria
[27] London Sch Hyg & Trop Med, London WC1, England
关键词
D O I
10.1158/1078-0432.CCR-04-2424
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To investigate the proportion of breast cancers arising inpatients with germ line BRCA1 and BRCA2 mutations expressing basal markers and developing predictive tests for identification of high-risk patients. Experimental Design: Histopathologic material from 182 tumors in BRCA1 mutation carriers, 63 BRCA2 carriers, and 109 controls, collected as part of the international Breast Cancer Linkage Consortium were immunohistochemically stained for CK14, CK5/6, CK17, epidermal growth factor receptor (EGFR), and osteonectin. Results: All five basal markers were commoner in BRCA1 tumors than in control tumors (CK14: 61% versus 12%; CK5/6: 58% versus 7%; CK17: 53% versus 10%; osteonectin: 43% versus 19%; EGFR: 67% versus 21%; P < 0.0001 in each case). In a multivariate analysis, CK14, CK5/6, and estrogen receptor (ER) remained significant predictors of BRCA1 carrier status. In contrast, the frequency of basal markers in BRCA2 tumors did not differ significant from controls. Conclusion: The use of cytokeratin staining in combination with ER and morphology provides a more accurate predictor of BRCA1 mutation status than previously available, that may be useful in selecting patients for BRCA1 mutation testing. The high percentage of BRCA1 cases positive for EGFR suggests that specific anti-tyrosine kinase therapy may be of potential benefit in these patients.
引用
收藏
页码:5175 / 5180
页数:6
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