Heterogenous high-level HER-2 amplification in a small subset of colorectal cancers.

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Heterogenous high-level HER-2 amplification in a small subset of colorectal cancers. / Marx, Andreas; Burandt, Eike Christian; Choschzick, Matthias; Simon, Ronald; Yekebas, Emre F.; Kaifi, Jussuf; Mirlacher, Martina; Atanackovic, Djordje; Bokemeyer, Carsten; Fiedler, Walter; Terracciano, Luigi; Sauter, Guido; Izbicki, Jakob R.

in: HUM PATHOL, Jahrgang 41, Nr. 11, 11, 2010, S. 1577-1585.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Marx, A, Burandt, EC, Choschzick, M, Simon, R, Yekebas, EF, Kaifi, J, Mirlacher, M, Atanackovic, D, Bokemeyer, C, Fiedler, W, Terracciano, L, Sauter, G & Izbicki, JR 2010, 'Heterogenous high-level HER-2 amplification in a small subset of colorectal cancers.', HUM PATHOL, Jg. 41, Nr. 11, 11, S. 1577-1585. <http://www.ncbi.nlm.nih.gov/pubmed/20656317?dopt=Citation>

APA

Marx, A., Burandt, E. C., Choschzick, M., Simon, R., Yekebas, E. F., Kaifi, J., Mirlacher, M., Atanackovic, D., Bokemeyer, C., Fiedler, W., Terracciano, L., Sauter, G., & Izbicki, J. R. (2010). Heterogenous high-level HER-2 amplification in a small subset of colorectal cancers. HUM PATHOL, 41(11), 1577-1585. [11]. http://www.ncbi.nlm.nih.gov/pubmed/20656317?dopt=Citation

Vancouver

Marx A, Burandt EC, Choschzick M, Simon R, Yekebas EF, Kaifi J et al. Heterogenous high-level HER-2 amplification in a small subset of colorectal cancers. HUM PATHOL. 2010;41(11):1577-1585. 11.

Bibtex

@article{887147b6d1a94c02bff0f536bb11c21e,
title = "Heterogenous high-level HER-2 amplification in a small subset of colorectal cancers.",
abstract = "HER-2 is the molecular target for antibody-based treatment of breast cancer (trastuzumab). The potential benefit of anti-HER-2 therapy is currently investigated in several other HER-2 amplified cancers. For example, trastuzumab was recently shown to be effective in HER-2 positive gastric cancer. To address the potential applicability of anti-HER-2 therapy in colorectal cancer, tissue microarray sections and colorectal resection specimens of 1851 colorectal cancers were analyzed for HER-2 overexpression and amplification using FDA approved reagents for immunohistochemistry and fluorescence in situ hybridization. HER-2 amplification was seen in 2.5% and HER-2 overexpression in 2.7% of 1439 interpretable colorectal cancers. Amplification was often high level with HER-2 copies ranging from 4 to 60 per tumor cell and was strongly related to protein overexpression. HER-2 amplification and overexpression were unrelated to histological tumor type, tumor localization, grading, pT, pN, pM or survival. As heterogeneity of drug target expression could represent a major drawback for targeted cancer therapy we next studied HER-2 heterogeneity in selected cases. Extensive evaluation of all available large sections from patients with HER-2 positive colorectal cancer revealed heterogenous findings in 3 of 4 cases. In summary, high-level HER-2 amplification occurs in a small fraction of colorectal cancers. Heterogeneity of amplification may limit the utility of anti- HER-2 therapy in some of these tumors and therefore, adequate clinical trials are needed to further evaluate this approach.",
author = "Andreas Marx and Burandt, {Eike Christian} and Matthias Choschzick and Ronald Simon and Yekebas, {Emre F.} and Jussuf Kaifi and Martina Mirlacher and Djordje Atanackovic and Carsten Bokemeyer and Walter Fiedler and Luigi Terracciano and Guido Sauter and Izbicki, {Jakob R.}",
year = "2010",
language = "Deutsch",
volume = "41",
pages = "1577--1585",
journal = "HUM PATHOL",
issn = "0046-8177",
publisher = "W.B. Saunders Ltd",
number = "11",

}

RIS

TY - JOUR

T1 - Heterogenous high-level HER-2 amplification in a small subset of colorectal cancers.

AU - Marx, Andreas

AU - Burandt, Eike Christian

AU - Choschzick, Matthias

AU - Simon, Ronald

AU - Yekebas, Emre F.

AU - Kaifi, Jussuf

AU - Mirlacher, Martina

AU - Atanackovic, Djordje

AU - Bokemeyer, Carsten

AU - Fiedler, Walter

AU - Terracciano, Luigi

AU - Sauter, Guido

AU - Izbicki, Jakob R.

PY - 2010

Y1 - 2010

N2 - HER-2 is the molecular target for antibody-based treatment of breast cancer (trastuzumab). The potential benefit of anti-HER-2 therapy is currently investigated in several other HER-2 amplified cancers. For example, trastuzumab was recently shown to be effective in HER-2 positive gastric cancer. To address the potential applicability of anti-HER-2 therapy in colorectal cancer, tissue microarray sections and colorectal resection specimens of 1851 colorectal cancers were analyzed for HER-2 overexpression and amplification using FDA approved reagents for immunohistochemistry and fluorescence in situ hybridization. HER-2 amplification was seen in 2.5% and HER-2 overexpression in 2.7% of 1439 interpretable colorectal cancers. Amplification was often high level with HER-2 copies ranging from 4 to 60 per tumor cell and was strongly related to protein overexpression. HER-2 amplification and overexpression were unrelated to histological tumor type, tumor localization, grading, pT, pN, pM or survival. As heterogeneity of drug target expression could represent a major drawback for targeted cancer therapy we next studied HER-2 heterogeneity in selected cases. Extensive evaluation of all available large sections from patients with HER-2 positive colorectal cancer revealed heterogenous findings in 3 of 4 cases. In summary, high-level HER-2 amplification occurs in a small fraction of colorectal cancers. Heterogeneity of amplification may limit the utility of anti- HER-2 therapy in some of these tumors and therefore, adequate clinical trials are needed to further evaluate this approach.

AB - HER-2 is the molecular target for antibody-based treatment of breast cancer (trastuzumab). The potential benefit of anti-HER-2 therapy is currently investigated in several other HER-2 amplified cancers. For example, trastuzumab was recently shown to be effective in HER-2 positive gastric cancer. To address the potential applicability of anti-HER-2 therapy in colorectal cancer, tissue microarray sections and colorectal resection specimens of 1851 colorectal cancers were analyzed for HER-2 overexpression and amplification using FDA approved reagents for immunohistochemistry and fluorescence in situ hybridization. HER-2 amplification was seen in 2.5% and HER-2 overexpression in 2.7% of 1439 interpretable colorectal cancers. Amplification was often high level with HER-2 copies ranging from 4 to 60 per tumor cell and was strongly related to protein overexpression. HER-2 amplification and overexpression were unrelated to histological tumor type, tumor localization, grading, pT, pN, pM or survival. As heterogeneity of drug target expression could represent a major drawback for targeted cancer therapy we next studied HER-2 heterogeneity in selected cases. Extensive evaluation of all available large sections from patients with HER-2 positive colorectal cancer revealed heterogenous findings in 3 of 4 cases. In summary, high-level HER-2 amplification occurs in a small fraction of colorectal cancers. Heterogeneity of amplification may limit the utility of anti- HER-2 therapy in some of these tumors and therefore, adequate clinical trials are needed to further evaluate this approach.

M3 - SCORING: Zeitschriftenaufsatz

VL - 41

SP - 1577

EP - 1585

JO - HUM PATHOL

JF - HUM PATHOL

SN - 0046-8177

IS - 11

M1 - 11

ER -