完整後設資料紀錄
DC 欄位語言
dc.contributor.authorHuang, Chung-Fengen_US
dc.contributor.authorYeh, Ming-Lunen_US
dc.contributor.authorHuang, Ching-Ien_US
dc.contributor.authorLiang, Po-Chengen_US
dc.contributor.authorLin, Yi-Hungen_US
dc.contributor.authorLin, Zu-Yauen_US
dc.contributor.authorChen, Shinn-Cherngen_US
dc.contributor.authorHuang, Jee-Fuen_US
dc.contributor.authorDai, Chia-Yenen_US
dc.contributor.authorChuang, Wan-Longen_US
dc.contributor.authorYu, Ming-Lungen_US
dc.date.accessioned2019-04-02T05:59:10Z-
dc.date.available2019-04-02T05:59:10Z-
dc.date.issued2018-11-01en_US
dc.identifier.issn1936-0533en_US
dc.identifier.urihttp://dx.doi.org/10.1007/s12072-018-9908-4en_US
dc.identifier.urihttp://hdl.handle.net/11536/148485-
dc.description.abstractBackground/aimsLiver fibrosis determined hepatocellular carcinoma (HCC) occurrence in chronic hepatitis C patients with sustained virological response (SVR). We aimed to determine whether post-treatment fibrotic modification overwhelmed pretreatment fibrotic status in terms of long-term HCC prediction.Methods265 SVR patients with paired biopsies before and after antiviral therapy were enrolled for analysis of the association of fibrotic changes with HCC.ResultsEighteen (6.8%) of the 265 patients developed HCC over 1931 person-years. Cox regression analysis without post-treatment fibrosis as a covariant revealed that factors predicted HCC included age (hazard ratio [HR]/confidence intervals [CI] 1.07/1.01-1.13, p=0.01), male gender (HR/CI 4.57/1.45-14.36, p=0.009), diabetes (HR/CI 3.60/1.32-9.85, p=0.01) and pretreatment advanced fibrosis (HR/CI 2.73/1.05-7.07, p=0.039). Advanced fibrosis in post-treatment status replaced pretreatment fibrosis as the most critical determinant of HCC when it was included for analysis (HR/CI 3.53/1.34-9.30, p=0.01). The incidences of HCC among patients with fibrotic modification from F0-2 to F0-2, F34 to F0-2, F0-2 to F34 and F34 to F34 were 0.41%, 0.84%, 1.68%, and 3.05%, respectively (p=0.004). Compared to patients whose fibrotic stage remained at F0-2 before and after treatment, the HCC risk decreased and did not differ among those whose fibrotic stage improved from F34 to F0-2. However, HCC risk increased significantly and gradually in patients whose fibrotic stages changed from F0-2 to F34 (HR/CI 4.13/1.11-15.36, p=0.035) and whose fibrotic stages remained at F34 before and after treatment (HR/CI 7.47/2.37-23.55, p=0.001) (trend p=0.003).ConclusionsPost-treatment fibrotic modifications overwhelmed pretreatment fibrotic statuses in predicting HCC.en_US
dc.language.isoen_USen_US
dc.subjectHCVen_US
dc.subjectHCCen_US
dc.subjectSVRen_US
dc.subjectFibrosisen_US
dc.subjectPost-treatmenten_US
dc.titlePost-treatment fibrotic modifications overwhelm pretreatment liver fibrosis in predicting HCC in CHC patients with curative antiviralsen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s12072-018-9908-4en_US
dc.identifier.journalHEPATOLOGY INTERNATIONALen_US
dc.citation.volume12en_US
dc.citation.spage544en_US
dc.citation.epage551en_US
dc.contributor.department生物科技學院zh_TW
dc.contributor.departmentCollege of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000450663900008en_US
dc.citation.woscount0en_US
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