• Medientyp: E-Artikel
  • Titel: A Virtual Microscopy System to Scan, Evaluate and Archive Biomarker Enhanced Cervical Cytology Slides
  • Beteiligte: Grabe, Niels; Lahrmann, Bernd; Pommerencke, Thora; von Knebel Doeberitz, Magnus; Reuschenbach, Miriam; Wentzensen, Nicolas
  • Erschienen: Hindawi Limited, 2010
  • Erschienen in: Analytical Cellular Pathology
  • Sprache: Englisch
  • DOI: 10.1155/2010/312048
  • ISSN: 2210-7177; 2210-7185
  • Schlagwörter: Cancer Research ; Cell Biology ; Molecular Medicine ; General Medicine ; Pathology and Forensic Medicine
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  • Beschreibung: <jats:p><jats:italic>Background</jats:italic>: Although cytological screening for cervical precancers has led to a reduction of cervical cancer incidence worldwide it is a subjective and variable method with low single-test sensitivity. New biomarkers like p16 that specifically highlight abnormal cervical cells can improve cytology performance. Virtual microscopy offers an ideal platform for assisted evaluation and archiving of biomarker-stained slides.</jats:p><jats:p><jats:italic>Methods</jats:italic>: We first performed a quantitative analysis of p16-stained slides digitized with the Hamamatsu NDP slide scanner. From the results an automated algorithm was created to reliably detect cells, nuclei and p16-stained cells. The algorithm's performance was evaluated on two complete slides and tiles from 52 independent slides (11,628, 4094 and 25,619 cells/clusters, respectively).</jats:p><jats:p><jats:italic>Results</jats:italic>: We achieved excellent performance to discriminate unstained cells from nuclei and biomarker-stained cells. The automated algorithm showed a high overall and positive agreement (99.0–99.7% and 70.9–83.4%, respectively) with the gold standard and had a very high sensitivity (89.1–100.0%) and specificity (98.9–100.0%) to detect biomarker-stained cells.</jats:p><jats:p><jats:italic>Conclusions</jats:italic>: We implemented a virtual microscopy system allowing highly efficient automated prescreening and archiving of biomarker-stained slides. Based on the initial results, we will evaluate the performance of our system in large epidemiologic studies against disease endpoints.</jats:p>
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