Cited 14 times in
Human chorionic gonadotrophin regression rate as a predictive factor of postmolar gestational trophoblastic neoplasm in high-risk hydatidiform mole: a case-control study
DC Field | Value | Language |
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dc.contributor.author | 김성훈 | - |
dc.contributor.author | 김영태 | - |
dc.contributor.author | 김재훈 | - |
dc.contributor.author | 김현기 | - |
dc.contributor.author | 남은지 | - |
dc.contributor.author | 조한별 | - |
dc.contributor.author | 김보욱 | - |
dc.contributor.author | 김상운 | - |
dc.date.accessioned | 2014-12-19T16:47:59Z | - |
dc.date.available | 2014-12-19T16:47:59Z | - |
dc.date.issued | 2012 | - |
dc.identifier.issn | 0301-2115 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/90216 | - |
dc.description.abstract | OBJECTIVE: The aim of this study was early prediction of postmolar gestational trophoblastic neoplasm (GTN) after evacuation of high-risk mole, by comparison of human chorionic gonadotrophin (hCG) regression rates. STUDY DESIGN: Fifty patients with a high-risk mole initially and spontaneously regressing after molar evacuation were selected from January 1, 1996 to May 31, 2010 (spontaneous regression group). Fifty patients with a high-risk mole initially and progressing to postmolar GTN after molar evacuation were selected (postmolar GTN group). hCG regression rates represented as hCG/initial hCG were compared between the two groups. The sensitivity and specificity of these rates for prediction of postmolar GTN were assessed using receiver operating characteristic curves. Multivariate analyses of associations between risk factors and postmolar GTN progression were performed. RESULTS: The mean regression rate of hCG between the two groups was compared. hCG regression rates represented as hCG/initial hCG (%) were 0.36% in the spontaneous regression group and 1.45% in the postmolar GTN group in the second week (p=0.003). Prediction of postmolar GTN by hCG regression rate revealed a sensitivity of 48.0% and specificity of 89.5% with a cut-off value of 0.716% and area under the curve (AUC) of 0.759 in the 2nd week (p<0.001). In patients with an hCG regression rate over 0.716% in the 2nd week, the hazard ratio for progression to postmolar GTN was 3.00 by multivariate analysis (p<0.001). CONCLUSION: Differences in hCG regression rates between spontaneous regression and postmolar GTN groups became evident from the second week following molar evacuation. The occurrence of postmolar GTN could be predicted as early as the second week by comparing regression rates. hCG regression rate is easily obtainable and a predictive factor for postmolar GTN. | - |
dc.description.statementOfResponsibility | open | - |
dc.relation.isPartOf | EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Case-Control Studies | - |
dc.subject.MESH | Chorionic Gonadotropin/blood* | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Gestational Trophoblastic Disease/etiology* | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Hydatidiform Mole/blood* | - |
dc.subject.MESH | Pregnancy | - |
dc.subject.MESH | Retrospective Studies | - |
dc.subject.MESH | Sensitivity and Specificity | - |
dc.subject.MESH | Uterine Neoplasms/blood* | - |
dc.title | Human chorionic gonadotrophin regression rate as a predictive factor of postmolar gestational trophoblastic neoplasm in high-risk hydatidiform mole: a case-control study | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Obstetrics & Gynecology (산부인과학) | - |
dc.contributor.googleauthor | Bo Wook Kim | - |
dc.contributor.googleauthor | Hanbyoul Cho | - |
dc.contributor.googleauthor | Hyunki Kim | - |
dc.contributor.googleauthor | Eun Ji Nam | - |
dc.contributor.googleauthor | Sang Wun Kim | - |
dc.contributor.googleauthor | Sunghoon Kim | - |
dc.contributor.googleauthor | Young Tae Kim | - |
dc.contributor.googleauthor | Jae-Hoon Kim | - |
dc.identifier.doi | 10.1016/j.ejogrb.2011.10.003 | - |
dc.admin.author | false | - |
dc.admin.mapping | false | - |
dc.contributor.localId | A00595 | - |
dc.contributor.localId | A00729 | - |
dc.contributor.localId | A00876 | - |
dc.contributor.localId | A01108 | - |
dc.contributor.localId | A01262 | - |
dc.contributor.localId | A03921 | - |
dc.contributor.localId | A00511 | - |
dc.contributor.localId | A00526 | - |
dc.relation.journalcode | J00834 | - |
dc.identifier.eissn | 1872-7654 | - |
dc.identifier.pmid | 22055909 | - |
dc.identifier.url | http://www.sciencedirect.com/science/article/pii/S0301211511005914 | - |
dc.subject.keyword | Hydatidiform mole | - |
dc.subject.keyword | Gestational trophoblastic neoplasm | - |
dc.subject.keyword | Human chorionic gonadotrophin | - |
dc.subject.keyword | Predictive factor | - |
dc.contributor.alternativeName | Kim, Sung Hoon | - |
dc.contributor.alternativeName | Kim, Young Tae | - |
dc.contributor.alternativeName | Kim, Jae Hoon | - |
dc.contributor.alternativeName | Kim, Hyun Ki | - |
dc.contributor.alternativeName | Nam, Eun Ji | - |
dc.contributor.alternativeName | Cho, Han Byoul | - |
dc.contributor.alternativeName | Kim, Bo Wook | - |
dc.contributor.alternativeName | Kim, Sang Wun | - |
dc.contributor.affiliatedAuthor | Kim, Sung Hoon | - |
dc.contributor.affiliatedAuthor | Kim, Young Tae | - |
dc.contributor.affiliatedAuthor | Kim, Jae Hoon | - |
dc.contributor.affiliatedAuthor | Kim, Hyun Ki | - |
dc.contributor.affiliatedAuthor | Nam, Eun Ji | - |
dc.contributor.affiliatedAuthor | Cho, Han Byoul | - |
dc.contributor.affiliatedAuthor | Kim, Bo Wook | - |
dc.contributor.affiliatedAuthor | Kim, Sang Wun | - |
dc.citation.volume | 160 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 100 | - |
dc.citation.endPage | 105 | - |
dc.identifier.bibliographicCitation | EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY, Vol.160(1) : 100-105, 2012 | - |
dc.identifier.rimsid | 34074 | - |
dc.type.rims | ART | - |
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