The basal subtype of breast carcinomas may represent the group of breast tumors that could benefit from EGFR-targeted therapies

被引:96
作者
Siziopikou, Kalliopi P. [1 ]
Cobteigh, Melody [2 ]
机构
[1] Rush Univ, Med Ctr, Dept Pathol, Chicago, IL 60612 USA
[2] Rush Univ, Med Ctr, Dept Med, Chicago, IL 60612 USA
关键词
basal subtype of breast carcinomas; breast cancer; EGFR; HER2; targeted therapies;
D O I
10.1016/j.breast.2006.09.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The recent understanding of the molecular basis of breast cancer growth and progression led to the identification of tumor subtypes with potentially different biologic behavior. In addition, targeted therapies are increasingly successful in cancer treatment. We recently reported that most of the ER-negative/PR-negative/HER2-negative patients, a group that presents a therapeutic challenge for the oncologist, express EGFR. We now report that the majority of these patients express cytokeratin CK5/6 and therefore belong to the basal subtype of breast carcinomas. These basal subtype lesions are usually high-grade tumors of ductal histology with a high proliferation rate. We propose that the majority of the "triple negative" patients have basal subtype tumors with high EGFR expression and that these tumors may be the subgroup of breast carcinomas that could potentially benefit the most from novel EGFR-targeted therapeutic strategies. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:104 / 107
页数:4
相关论文
共 26 条
  • [21] SARTOR CI, 2004, BREAST CANC RES S34, V88
  • [22] Siziopikou KP, 2004, BREAST CANCER RES TR, V88, pS24
  • [23] Use of chemotherapy plus a monoclonal antibody against HER2 for metastatic breast cancer that overexpresses HER2.
    Slamon, DJ
    Leyland-Jones, B
    Shak, S
    Fuchs, H
    Paton, V
    Bajamonde, A
    Fleming, T
    Eiermann, W
    Wolter, J
    Pegram, M
    Baselga, J
    Norton, L
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (11) : 783 - 792
  • [24] Gene expression patterns of breast carcinomas distinguish tumor subclasses with clinical implications
    Sorlie, T
    Perou, CM
    Tibshirani, R
    Aas, T
    Geisler, S
    Johnsen, H
    Hastie, T
    Eisen, MB
    van de Rijn, M
    Jeffrey, SS
    Thorsen, T
    Quist, H
    Matese, JC
    Brown, PO
    Botstein, D
    Lonning, PE
    Borresen-Dale, AL
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (19) : 10869 - 10874
  • [25] Study of the biologic effects of lapatinib, a reversible inhibitor of ErbB1 and ErbB2 tyrosine kinases, on tumor growth and survival pathways in patients with advanced malignancies
    Spector, NL
    Xia, WL
    Burris, H
    Hurwitz, H
    Dees, EC
    Dowlati, A
    O'Neil, B
    Overmoyer, B
    Marcom, PK
    Blackwell, KL
    Smith, DA
    Koch, KM
    Stead, A
    Mangum, S
    Ellis, MJ
    Liu, LH
    Man, AK
    Bremer, TM
    Harris, J
    Bacus, S
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (11) : 2502 - 2512
  • [26] Gene expression profiling predicts clinical outcome of breast cancer
    van't Veer, LJ
    Dai, HY
    van de Vijver, MJ
    He, YDD
    Hart, AAM
    Mao, M
    Peterse, HL
    van der Kooy, K
    Marton, MJ
    Witteveen, AT
    Schreiber, GJ
    Kerkhoven, RM
    Roberts, C
    Linsley, PS
    Bernards, R
    Friend, SH
    [J]. NATURE, 2002, 415 (6871) : 530 - 536