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Identification of lung cancer with high sensitivity and specificity by blood testing

BACKGROUND: Lung cancer is a very frequent and lethal tumor with an identifiable risk population. Cytological analysis and chest X-ray failed to reduce mortality, and CT screenings are still controversially discussed. Recent studies provided first evidence for the potential usefulness of autoantigen...

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Detalles Bibliográficos
Autores principales: Leidinger, Petra, Keller, Andreas, Heisel, Sabrina, Ludwig, Nicole, Rheinheimer, Stefanie, Klein, Veronika, Andres, Claudia, Staratschek-Jox, Andrea, Wolf, Jürgen, Stoelben, Erich, Stephan, Bernhard, Stehle, Ingo, Hamacher, Jürg, Huwer, Hanno, Lenhof, Hans-Peter, Meese, Eckart
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2832627/
https://www.ncbi.nlm.nih.gov/pubmed/20146812
http://dx.doi.org/10.1186/1465-9921-11-18
Descripción
Sumario:BACKGROUND: Lung cancer is a very frequent and lethal tumor with an identifiable risk population. Cytological analysis and chest X-ray failed to reduce mortality, and CT screenings are still controversially discussed. Recent studies provided first evidence for the potential usefulness of autoantigens as markers for lung cancer. METHODS: We used extended panels of arrayed antigens and determined autoantibody signatures of sera from patients with different kinds of lung cancer, different common non-tumor lung pathologies, and controls without any lung disease by a newly developed computer aided image analysis procedure. The resulting signatures were classified using linear kernel Support Vector Machines and 10-fold cross-validation. RESULTS: The novel approach allowed for discriminating lung cancer patients from controls without any lung disease with a specificity of 97.0%, a sensitivity of 97.9%, and an accuracy of 97.6%. The classification of stage IA/IB tumors and controls yielded a specificity of 97.6%, a sensitivity of 75.9%, and an accuracy of 92.9%. The discrimination of lung cancer patients from patients with non-tumor lung pathologies reached an accuracy of 88.5%. CONCLUSION: We were able to separate lung cancer patients from subjects without any lung disease with high accuracy. Furthermore, lung cancer patients could be seprated from patients with other non-tumor lung diseases. These results provide clear evidence that blood-based tests open new avenues for the early diagnosis of lung cancer.