Strong HER-2/neu protein overexpression by immunohistochemistry often does not predict oncogene amplification by fluorescence in situ hybridization

被引:78
作者
Hammock, L [1 ]
Lewis, M [1 ]
Phillips, C [1 ]
Cohen, C [1 ]
机构
[1] Emory Univ Hosp, Dept Pathol & Lab Med, Atlanta, GA 30322 USA
关键词
immunohistochemistry; HER-2/neu; fluorescent in situ hybridization; breast carcinoma;
D O I
10.1053/S0046-8177(03)00409-X
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Breast cancer patients with HER-2/neu oncogene amplification by fluorescence in situ hybridization (FISH) have been shown to have a better response to trastuzumab (Herceptin) therapy than those showing HER-2/neu protein overexpression only. Many centers currently perform FISH only on tumors showing 2+ HER-2/neu positivity by immunohistochemistry (IHC), with the assumption that 3+ positivity virtually equates with amplification. Results of FISH performed on 102 breast cancer cases over a 12-month period were correlated with HER-2/neu IHC results. FISH was performed using a ratio of HER-2/neu and chromosome 17 centromere signal counts (PathVysion; Vysis, Downers Grove, IL). Immunohistochemical expression of HER-2/neu was evaluated according to the published scoring guidelines of the HercepTest (Dako, Carpinteria, CA): Only 22 of 45 tumors with 3+ positivity (49%) showed amplification by FISH. Only 2 of 25 cases with 2+ staining by IHC (6%) showed gene amplification, and 1 of 25 cases with negative IHC staining (4%) showed weak amplification. Of the 25 cases showing oncogene amplification, 22 (88%) showed 3+ IHC positivity, 2 (8%) showed 2+ positivity, and 1 (4%) was negative by IHC. More than 50% of breast tumors showing strong 3+ HER-2/neu staining do not show oncogene amplification by FISH. Most tumors with 2+ and negative IHC also fail to amplify. In our experience, FISH studies should be performed on all 3+ and 2+ staining tumors to avoid inappropriate and toxic treatment. The decision to perform FISH on IHC-negative tumors should be guided by additional parameters, including tumor grade and estrogen receptor status. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:1043 / 1047
页数:5
相关论文
共 25 条
[1]   THE NEU ONCOGENE ENCODES AN EPIDERMAL GROWTH-FACTOR RECEPTOR-RELATED PROTEIN [J].
BARGMANN, CI ;
HUNG, MC ;
WEINBERG, RA .
NATURE, 1986, 319 (6050) :226-230
[2]   Strong correlation between results of fluorescent in situ hybridization and immunohistochemistry for the assessment of the ERBB2 (HER-2/neu) gene status in breast carcinoma [J].
Couturier, J ;
Vincent-Salomon, A ;
Nicolas, A ;
Beuzeboc, P ;
Mouret, E ;
Zafrani, B ;
Sastre-Garau, X .
MODERN PATHOLOGY, 2000, 13 (11) :1238-1243
[3]   HETERODIMERIZATION AND FUNCTIONAL INTERACTION BETWEEN EGF RECEPTOR FAMILY MEMBERS - A NEW SIGNALING PARADIGM WITH IMPLICATIONS FOR BREAST-CANCER RESEARCH [J].
EARP, HS ;
DAWSON, TL ;
LI, X ;
YU, H .
BREAST CANCER RESEARCH AND TREATMENT, 1995, 35 (01) :115-132
[4]  
FIEBELKORN KR, 2000, MODERN PATHOL, V13, pA222
[5]   Regulatory issues in tumor marker development [J].
Gutman, S .
SEMINARS IN ONCOLOGY, 2002, 29 (03) :294-300
[6]   HER-2/neu gene amplification compared with HER-2/neu protein overexpression and interobserver reproducibility in invasive breast carcinoma [J].
Hoang, MP ;
Sahin, AA ;
Ordòñez, NG ;
Sneige, N .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2000, 113 (06) :852-859
[7]   HER-2/neu protein expression in breast cancer evaluated by immunohistochemistry - A study of interlaboratory agreement [J].
Jacobs, TW ;
Gown, AM ;
Yaziji, H ;
Barnes, MJ ;
Schnitt, SJ .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2000, 113 (02) :251-258
[8]   Protein overexpression and gene amplification of c-erbB-2 in breast carcinomas:: A comparative study of immunohistochemistry and fluorescence in situ hybridization of formalin-fixed, paraffin-embedded tissues [J].
Kobayashi, M ;
Ooi, A ;
Oda, Y ;
Nakanishi, I .
HUMAN PATHOLOGY, 2002, 33 (01) :21-28
[9]  
KONECNY G, 2001, P AN M AM SOC CLIN, V20, P46
[10]   HER-2/neu analysis in archival tissue samples of human breast cancer:: Comparison of immunohistochemistry and fluorescence in situ hybridization [J].
Lebeau, A ;
Deimling, D ;
Kaltz, C ;
Sendelhofert, A ;
Iff, A ;
Luthardt, B ;
Untch, M ;
Löhrs, U .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (02) :354-363