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Diagnostic performance of CA 125, HE4, and risk of Ovarian Malignancy Algorithm for ovarian cancer

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dc.contributor.author이경아-
dc.date.accessioned2019-12-18T01:21:34Z-
dc.date.available2019-12-18T01:21:34Z-
dc.date.issued2019-
dc.identifier.issn0887-8013-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/173480-
dc.description.abstractOBJECTIVE: We evaluated the diagnostic performance of CA 125, HE4, and ROMA for ovarian cancer in Koreans and set optimal cutoffs. METHOD: Serum levels of HE4 and CA 125 and the ROMA score were determined in 762 patients with benign gynecological disease and 70 with ovarian cancer. Receiver operating characteristic curves were constructed to calculate the areas under the curve (AUC). CA 125, HE4, and ROMA exhibiting maximum Youden index were determined, respectively, as the optimal cutoffs, and sensitivity and specificity were evaluated by applying those cutoffs. RESULTS: In benign diseases, CA 125 significantly increased in patients with uterine myoma, adenomyosis, endometrial pathology, or endometriosis, but HE4 only increased in patients with adenomyosis. For the diagnosis of ovarian cancer, the combination of CA 125, HE4, and age showed the highest AUC value of 0.892 in the premenopausal group, and ROMA demonstrated the best diagnostic performance, with an AUC of 0.935 in postmenopausal patients. When the optimal cutoff values for CA 125 and HE4 were applied, the sensitivities of CA 125, HE4, and ROMA in premenopausal women were all the same at 0.714, while the specificities were 0.841, 0.974, and 0.972, respectively. In the postmenopausal group, the sensitivities of these markers were 0.857, 0.804, and 0.929, and the specificities were 0.836, 0.887, and 0.800, respectively. CONCLUSION: Although all markers demonstrated good diagnostic performance, they varied depending on the pathologic types of benign diseases and ovarian cancer. For accurate diagnosis of ovarian cancer, CA 125, HE4, and ROMA should be used complementarily.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherWiley-Liss, Inc.-
dc.relation.isPartOfJOURNAL OF CLINICAL LABORATORY ANALYSIS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAlgorithms-
dc.subject.MESHBiomarkers, Tumor/blood-
dc.subject.MESHCA-125 Antigen/blood*-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHMenopause-
dc.subject.MESHMiddle Aged-
dc.subject.MESHOvarian Neoplasms/blood-
dc.subject.MESHOvarian Neoplasms/diagnosis*-
dc.subject.MESHOvarian Neoplasms/epidemiology-
dc.subject.MESHOvarian Neoplasms/pathology-
dc.subject.MESHProteins/analysis*-
dc.subject.MESHRisk-
dc.subject.MESHSensitivity and Specificity-
dc.titleDiagnostic performance of CA 125, HE4, and risk of Ovarian Malignancy Algorithm for ovarian cancer-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Laboratory Medicine (진단검사의학교실)-
dc.contributor.googleauthorBoyeon Kim-
dc.contributor.googleauthorYongjung Park-
dc.contributor.googleauthorBanseok Kim-
dc.contributor.googleauthorHyo Jun Ahn-
dc.contributor.googleauthorKyung‐A Lee-
dc.contributor.googleauthorJae Eun Chung-
dc.contributor.googleauthorSang Won Han-
dc.identifier.doi10.1002/jcla.22624-
dc.contributor.localIdA02647-
dc.relation.journalcodeJ01323-
dc.identifier.eissn1098-2825-
dc.identifier.pmid30009497-
dc.contributor.alternativeNameLee, Kyung A-
dc.contributor.affiliatedAuthor이경아-
dc.citation.volume33-
dc.citation.number1-
dc.citation.startPagee22624-
dc.identifier.bibliographicCitationJOURNAL OF CLINICAL LABORATORY ANALYSIS, Vol.33(1) : e22624, 2019-
dc.identifier.rimsid64364-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학교실) > 1. Journal Papers

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