Ep-CAM expression in squamous cell carcinoma of the esophagus: a potential therapeutic target and prognostic marker.

Standard

Ep-CAM expression in squamous cell carcinoma of the esophagus: a potential therapeutic target and prognostic marker. / Stoecklein, Nikolas H; Siegmund, Annika; Scheunemann, Peter; Luebke, Andreas M; Erbersdobler, Andreas; Verde, Pablo E; Eisenberger, Claus F; Peiper, Matthias; Rehders, Alexander; Esch, Jan Schulte Am; Knoefel, Wolfram Trudo; Hosch, Stefan B.

in: BMC CANCER, Jahrgang 6, 2006, S. 165.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Stoecklein, NH, Siegmund, A, Scheunemann, P, Luebke, AM, Erbersdobler, A, Verde, PE, Eisenberger, CF, Peiper, M, Rehders, A, Esch, JSA, Knoefel, WT & Hosch, SB 2006, 'Ep-CAM expression in squamous cell carcinoma of the esophagus: a potential therapeutic target and prognostic marker.', BMC CANCER, Jg. 6, S. 165. https://doi.org/10.1186/1471-2407-6-165

APA

Stoecklein, N. H., Siegmund, A., Scheunemann, P., Luebke, A. M., Erbersdobler, A., Verde, P. E., Eisenberger, C. F., Peiper, M., Rehders, A., Esch, J. S. A., Knoefel, W. T., & Hosch, S. B. (2006). Ep-CAM expression in squamous cell carcinoma of the esophagus: a potential therapeutic target and prognostic marker. BMC CANCER, 6, 165. https://doi.org/10.1186/1471-2407-6-165

Vancouver

Bibtex

@article{1403c471707942968be9460f2e6948d8,
title = "Ep-CAM expression in squamous cell carcinoma of the esophagus: a potential therapeutic target and prognostic marker.",
abstract = "BACKGROUND: To evaluate the expression and test the clinical significance of the epithelial cellular adhesion molecule (Ep-CAM) in esophageal squamous cell carcinoma (SCC) to check the suitability of esophageal SCC patients for Ep-CAM directed targeted therapies. METHODS: The Ep-CAM expression was immunohistochemically investigated in 70 primary esophageal SCCs using the monoclonal antibody Ber-EP4. For the interpretation of the staining results, we used a standardized scoring system ranging from 0 to 3+. The survival analysis was calculated from 53 patients without distant metastasis, with R0 resection and at least 2 months of clinical follow-up. RESULTS: Ep-CAM neo-expression was observed in 79% of the tumors with three expression levels, 1+ (26%), 2+ (11%) and 3+ (41%). Heterogeneous expression was observed at all expression levels. Interestingly, tumors with 3+ Ep-CAM expression conferred a significantly decreased median relapse-free survival period (log rank, p = 0.0001) and median overall survival (log rank, p = 0.0003). Multivariate survival analysis disclosed Ep-CAM 3+ expression as independent prognostic factor. CONCLUSION: Our results suggest Ep-CAM as an attractive molecule for targeted therapy in esophageal SCC. Considering the discontenting results of the current adjuvant concepts for esophageal SCC patients, Ep-CAM might provide a promising target for an adjuvant immunotherapeutic intervention.",
author = "Stoecklein, {Nikolas H} and Annika Siegmund and Peter Scheunemann and Luebke, {Andreas M} and Andreas Erbersdobler and Verde, {Pablo E} and Eisenberger, {Claus F} and Matthias Peiper and Alexander Rehders and Esch, {Jan Schulte Am} and Knoefel, {Wolfram Trudo} and Hosch, {Stefan B}",
year = "2006",
doi = "10.1186/1471-2407-6-165",
language = "Deutsch",
volume = "6",
pages = "165",
journal = "BMC CANCER",
issn = "1471-2407",
publisher = "BioMed Central Ltd.",

}

RIS

TY - JOUR

T1 - Ep-CAM expression in squamous cell carcinoma of the esophagus: a potential therapeutic target and prognostic marker.

AU - Stoecklein, Nikolas H

AU - Siegmund, Annika

AU - Scheunemann, Peter

AU - Luebke, Andreas M

AU - Erbersdobler, Andreas

AU - Verde, Pablo E

AU - Eisenberger, Claus F

AU - Peiper, Matthias

AU - Rehders, Alexander

AU - Esch, Jan Schulte Am

AU - Knoefel, Wolfram Trudo

AU - Hosch, Stefan B

PY - 2006

Y1 - 2006

N2 - BACKGROUND: To evaluate the expression and test the clinical significance of the epithelial cellular adhesion molecule (Ep-CAM) in esophageal squamous cell carcinoma (SCC) to check the suitability of esophageal SCC patients for Ep-CAM directed targeted therapies. METHODS: The Ep-CAM expression was immunohistochemically investigated in 70 primary esophageal SCCs using the monoclonal antibody Ber-EP4. For the interpretation of the staining results, we used a standardized scoring system ranging from 0 to 3+. The survival analysis was calculated from 53 patients without distant metastasis, with R0 resection and at least 2 months of clinical follow-up. RESULTS: Ep-CAM neo-expression was observed in 79% of the tumors with three expression levels, 1+ (26%), 2+ (11%) and 3+ (41%). Heterogeneous expression was observed at all expression levels. Interestingly, tumors with 3+ Ep-CAM expression conferred a significantly decreased median relapse-free survival period (log rank, p = 0.0001) and median overall survival (log rank, p = 0.0003). Multivariate survival analysis disclosed Ep-CAM 3+ expression as independent prognostic factor. CONCLUSION: Our results suggest Ep-CAM as an attractive molecule for targeted therapy in esophageal SCC. Considering the discontenting results of the current adjuvant concepts for esophageal SCC patients, Ep-CAM might provide a promising target for an adjuvant immunotherapeutic intervention.

AB - BACKGROUND: To evaluate the expression and test the clinical significance of the epithelial cellular adhesion molecule (Ep-CAM) in esophageal squamous cell carcinoma (SCC) to check the suitability of esophageal SCC patients for Ep-CAM directed targeted therapies. METHODS: The Ep-CAM expression was immunohistochemically investigated in 70 primary esophageal SCCs using the monoclonal antibody Ber-EP4. For the interpretation of the staining results, we used a standardized scoring system ranging from 0 to 3+. The survival analysis was calculated from 53 patients without distant metastasis, with R0 resection and at least 2 months of clinical follow-up. RESULTS: Ep-CAM neo-expression was observed in 79% of the tumors with three expression levels, 1+ (26%), 2+ (11%) and 3+ (41%). Heterogeneous expression was observed at all expression levels. Interestingly, tumors with 3+ Ep-CAM expression conferred a significantly decreased median relapse-free survival period (log rank, p = 0.0001) and median overall survival (log rank, p = 0.0003). Multivariate survival analysis disclosed Ep-CAM 3+ expression as independent prognostic factor. CONCLUSION: Our results suggest Ep-CAM as an attractive molecule for targeted therapy in esophageal SCC. Considering the discontenting results of the current adjuvant concepts for esophageal SCC patients, Ep-CAM might provide a promising target for an adjuvant immunotherapeutic intervention.

U2 - 10.1186/1471-2407-6-165

DO - 10.1186/1471-2407-6-165

M3 - SCORING: Zeitschriftenaufsatz

VL - 6

SP - 165

JO - BMC CANCER

JF - BMC CANCER

SN - 1471-2407

ER -