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Computerized patient identification for the EMBRACA clinical trial using real-time data from the PRAEGNANT network for metastatic breast cancer patients.
Hein, Alexander; Gass, Paul; Walter, Christina Barbara; Taran, Florin-Andrei; Hartkopf, Andreas; Overkamp, Friedrich; Kolberg, Hans-Christian; Hadji, Peyman; Tesch, Hans; Ettl, Johannes; Wuerstlein, Rachel; Lounsbury, Debra; Lux, Michael P; Lüftner, Diana; Wallwiener, Markus; Müller, Volkmar; Belleville, Erik; Janni, Wolfgang; Fehm, Tanja N; Wallwiener, Diethelm; Ganslandt, Thomas; Ruebner, Matthias; Beckmann, Matthias W; Schneeweiss, Andreas; Fasching, Peter A; Brucker, Sara Y.
Afiliación
  • Hein A; Department of Gynecology and Obstetrics, Comprehensive Cancer Center Erlangen-EMN, Friedrich-Alexander, Erlangen University Hospital University of Erlangen-Nuremberg, Universitätsstrasse 21-23, 91054, Erlangen, Germany.
  • Gass P; Department of Gynecology and Obstetrics, Comprehensive Cancer Center Erlangen-EMN, Friedrich-Alexander, Erlangen University Hospital University of Erlangen-Nuremberg, Universitätsstrasse 21-23, 91054, Erlangen, Germany.
  • Walter CB; Department of Obstetrics and Gynecology, University of Tübingen, Tübingen, Germany.
  • Taran FA; Department of Obstetrics and Gynecology, University of Tübingen, Tübingen, Germany.
  • Hartkopf A; Department of Obstetrics and Gynecology, University of Tübingen, Tübingen, Germany.
  • Overkamp F; Outpatient Department of Hematology and Oncology, Recklinghausen, Germany.
  • Kolberg HC; Marienhospital Bottrop, Bottrop, Germany.
  • Hadji P; Nordwest Hospital, Frankfurt, Germany.
  • Tesch H; Onkologie Bethanien, Frankfurt, Germany.
  • Ettl J; Department of Obstetrics and Gynecology, Technical University of Munich, Munich, Germany.
  • Wuerstlein R; Department of Gynecology and Obstetrics and Comprehensive Cancer Center, Ludwig Maximilian University, Munich, Germany.
  • Lounsbury D; BioMarin Pharmaceutical Inc, San Rafael, CA, USA.
  • Lux MP; Department of Gynecology and Obstetrics, Comprehensive Cancer Center Erlangen-EMN, Friedrich-Alexander, Erlangen University Hospital University of Erlangen-Nuremberg, Universitätsstrasse 21-23, 91054, Erlangen, Germany.
  • Lüftner D; Department of Hematology, Oncology and Tumour ImmunologyCharité, University Hospital, Campus Benjamin Franklin, Berlin, Germany.
  • Wallwiener M; Department of Obstetrics and Gynecology, University of Heidelberg, Heidelberg, Germany.
  • Müller V; Department of Gynecology, Hamburg-Eppendorf University Medical Center, Hamburg, Germany.
  • Belleville E; Clin-Sol Ltd, Würzburg, Germany.
  • Janni W; Department of Gynecology and Obstetrics, Ulm University Hospital, Ulm, Germany.
  • Fehm TN; Department of Gynecology and Obstetrics, Heinrich Heine University of Düsseldorf, Düsseldorf, Germany.
  • Wallwiener D; Department of Obstetrics and Gynecology, University of Tübingen, Tübingen, Germany.
  • Ganslandt T; Chair of Medical Informatics, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen, Germany.
  • Ruebner M; Department of Gynecology and Obstetrics, Comprehensive Cancer Center Erlangen-EMN, Friedrich-Alexander, Erlangen University Hospital University of Erlangen-Nuremberg, Universitätsstrasse 21-23, 91054, Erlangen, Germany.
  • Beckmann MW; Institut Fuer Frauengesundheit GmbH, Erlangen, Germany.
  • Schneeweiss A; Department of Gynecology and Obstetrics, Comprehensive Cancer Center Erlangen-EMN, Friedrich-Alexander, Erlangen University Hospital University of Erlangen-Nuremberg, Universitätsstrasse 21-23, 91054, Erlangen, Germany.
  • Fasching PA; National Center for Tumor Diseases and Department of Gynecology and Obstetrics, Heidelberg University Hospital, Heidelberg, Germany.
  • Brucker SY; Department of Gynecology and Obstetrics, Comprehensive Cancer Center Erlangen-EMN, Friedrich-Alexander, Erlangen University Hospital University of Erlangen-Nuremberg, Universitätsstrasse 21-23, 91054, Erlangen, Germany. peter.fasching@uk-erlangen.de.
Breast Cancer Res Treat ; 158(1): 59-65, 2016 07.
Article en En | MEDLINE | ID: mdl-27283834
ABSTRACT
As breast cancer is a diverse disease, clinical trials are becoming increasingly diversified and are consequently being conducted in very small subgroups of patients, making study recruitment increasingly difficult. The aim of this study was to assess the use of data from a remote data entry system that serves a large national registry for metastatic breast cancer. The PRAEGNANT network is a real-time registry with an integrated biomaterials bank that was designed as a scientific study and as a means of identifying patients who are eligible for clinical trials, based on clinical and molecular information. Here, we report on the automated use of the clinical data documented to identify patients for a clinical trial (EMBRACA) for patients with metastatic breast cancer. The patients' charts were assessed by two independent physicians involved in the clinical trial and also by a computer program that tested patients for eligibility using a structured query language script. In all, 326 patients from two study sites in the PRAEGNANT network were included in the analysis. Using expert assessment, 120 of the 326 patients (37 %) appeared to be eligible for inclusion in the EMBRACA study; with the computer algorithm assessment, a total of 129 appeared to be eligible. The sensitivity of the computer algorithm was 0.87 and its specificity was 0.88. Using computer-based identification of patients for clinical trials appears feasible. With the instrument's high specificity, its application in a large cohort of patients appears to be feasible, and the workload for reassessing the patients is limited.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Selección de Paciente Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans Idioma: En Revista: Breast Cancer Res Treat Año: 2016 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Selección de Paciente Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans Idioma: En Revista: Breast Cancer Res Treat Año: 2016 Tipo del documento: Article País de afiliación: Alemania