Linked Life Data

11531010

Source:http://linkedlifedata.com/resource/pubmed/id/11531010

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pubmed-article:11531010pubmed:abstractTextOur purpose was to determine whether peripheral blood biomarkers MUC1 and CK19 could be used to complement imaging studies in differentiating benign from malignant indeterminate pulmonary nodules or masses detected on computed tomography CT. One hundred and eighteen patients had a thoracic CT and blood drawn for tumor marker reverse transcriptase-polymerase chain reaction analysis. Thirty-five of the 118 patients had an indeterminate pulmonary nodular opacity on CT, and the findings then were correlated with the reverse transcriptase-polymerase chain reaction results. The sensitivity and specificity for the markers in determining malignancy was calculated. Thirteen of the 35 opacities on CT proved to be benign, and 22 proved to be lung cancer. Among the patients with indeterminate pulmonary abnormalities, polymorphic epithelial mucin protein 1 had a sensitivity and specificity for lung cancer of 100% and 46%, respectively. Cytokeratin 19 had a sensitivity and specificity for lung cancer of 95% and 8%, respectively. These preliminary data showed that serum biomarkers polymorphic epithelial mucin protein 1 and cytokeratin 19 were not specific for lung cancer, although patients with an indeterminate pulmonary abnormality and negative markers were unlikely to have lung cancer. Integration of imaging studies with the appropriate biomarkers may prove useful in evaluating indeterminate pulmonary nodules or masses.lld:pubmed
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pubmed-article:11531010pubmed:pagination336-43lld:pubmed
pubmed-article:11531010pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:11531010pubmed:year2001lld:pubmed
pubmed-article:11531010pubmed:articleTitleIntegration of peripheral blood biomarkers with computed tomography to differentiate benign from malignant pulmonary opacities.lld:pubmed
pubmed-article:11531010pubmed:affiliationDuke University Medical Center, Department of Surgery, Durham, NC 27710, USA.lld:pubmed
pubmed-article:11531010pubmed:publicationTypeJournal Articlelld:pubmed