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Detection of soluble EpCAM (sEpCAM) in malignant ascites predicts poor overall survival in patients treated with catumaxomab.
Seeber, Andreas; Braicu, Ioana; Untergasser, Gerold; Nassir, Mani; Fong, Dominic; Botta, Laura; Gastl, Guenther; Fiegl, Heidi; Zeimet, Alain; Sehouli, Jalid; Spizzo, Gilbert.
Afiliación
  • Seeber A; Department of Haematology and Oncology, Innsbruck Medical University, Innsbruck, Austria.
  • Braicu I; Tyrolean Cancer Research Institute, Innsbruck, Austria.
  • Untergasser G; Oncotyrol - Center for Personalized Cancer Medicine, Innsbruck, Austria.
  • Nassir M; European Competence Center for Ovarian Cancer, Charité Berlin, Berlin, Germany.
  • Fong D; Department of Haematology and Oncology, Innsbruck Medical University, Innsbruck, Austria.
  • Botta L; Tyrolean Cancer Research Institute, Innsbruck, Austria.
  • Gastl G; Oncotyrol - Center for Personalized Cancer Medicine, Innsbruck, Austria.
  • Fiegl H; European Competence Center for Ovarian Cancer, Charité Berlin, Berlin, Germany.
  • Zeimet A; Department of Haematology and Oncology, Innsbruck Medical University, Innsbruck, Austria.
  • Sehouli J; Tyrolean Cancer Research Institute, Innsbruck, Austria.
  • Spizzo G; Oncotyrol - Center for Personalized Cancer Medicine, Innsbruck, Austria.
Oncotarget ; 6(28): 25017-23, 2015 Sep 22.
Article en En | MEDLINE | ID: mdl-26296970
EpCAM is an attractive target for cancer therapy and the EpCAM-specific antibody catumaxomab has been used for intraperitoneal treatment of EpCAM-positive cancer patients with malignant ascites. New prognostic markers are necessary to select patients that mostly benefit from catumaxomab. Recent data showed that soluble EpCAM (sEpCAM) is capable to block the effect of catumaxomab in vitro. This exploratory retrospective analysis was performed on archived ascites samples to evaluate the predictive role of sEpCAM in catumaxomab-treated patients. Sixty-six catumaxomab-treated patients with an available archived ascites sample were included in this study and tested for sEpCAM by sandwich ELISA. All probes were sampled before treatment start and all patients received at least one catumaxomab infusion. Overall survival, puncture-free survival and time to next puncture were compared between sEpCAM-positive and -negative patients. We detected sEpCAM in ascites samples of 9 patients (13.6%). These patients showed a significantly shorter overall survival. The prognostic significance of sEpCAM in ascites was particularly strong in patients with ovarian cancer. Puncture-free survival and time to next puncture were not significantly different between sEpCAM-positive and -negative patients. We propose sEpCAM in malignant ascites as a potential predictive marker in cancer patients treated with catumaxomab. Prospective studies with larger patients samples are urgently needed to confirm these findings and studies testing dose-intensified catumaxomab in patients with sEpCAM-positive ascites should be envisaged.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ascitis / Biomarcadores de Tumor / Moléculas de Adhesión Celular / Anticuerpos Biespecíficos / Antígenos de Neoplasias Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Oncotarget Año: 2015 Tipo del documento: Article País de afiliación: Austria

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ascitis / Biomarcadores de Tumor / Moléculas de Adhesión Celular / Anticuerpos Biespecíficos / Antígenos de Neoplasias Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Oncotarget Año: 2015 Tipo del documento: Article País de afiliación: Austria