完整後設資料紀錄
DC 欄位 | 值 | 語言 |
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dc.contributor.author | Huang, Chung-Feng | en_US |
dc.contributor.author | Yeh, Ming-Lun | en_US |
dc.contributor.author | Huang, Ching-I | en_US |
dc.contributor.author | Liang, Po-Cheng | en_US |
dc.contributor.author | Lin, Yi-Hung | en_US |
dc.contributor.author | Lin, Zu-Yau | en_US |
dc.contributor.author | Chen, Shinn-Cherng | en_US |
dc.contributor.author | Huang, Jee-Fu | en_US |
dc.contributor.author | Dai, Chia-Yen | en_US |
dc.contributor.author | Chuang, Wan-Long | en_US |
dc.contributor.author | Yu, Ming-Lung | en_US |
dc.date.accessioned | 2019-04-02T05:59:10Z | - |
dc.date.available | 2019-04-02T05:59:10Z | - |
dc.date.issued | 2018-11-01 | en_US |
dc.identifier.issn | 1936-0533 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1007/s12072-018-9908-4 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/148485 | - |
dc.description.abstract | Background/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.iso | en_US | en_US |
dc.subject | HCV | en_US |
dc.subject | HCC | en_US |
dc.subject | SVR | en_US |
dc.subject | Fibrosis | en_US |
dc.subject | Post-treatment | en_US |
dc.title | Post-treatment fibrotic modifications overwhelm pretreatment liver fibrosis in predicting HCC in CHC patients with curative antivirals | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1007/s12072-018-9908-4 | en_US |
dc.identifier.journal | HEPATOLOGY INTERNATIONAL | en_US |
dc.citation.volume | 12 | en_US |
dc.citation.spage | 544 | en_US |
dc.citation.epage | 551 | en_US |
dc.contributor.department | 生物科技學院 | zh_TW |
dc.contributor.department | College of Biological Science and Technology | en_US |
dc.identifier.wosnumber | WOS:000450663900008 | en_US |
dc.citation.woscount | 0 | en_US |
顯示於類別: | 期刊論文 |