Liver transplantation for HBV-related liver disease: impact of prophylaxis for HBV on HCC recurrence
Conflicting data exist regarding optimal prophylaxis for HBV recurrence (HBV-R) after liver transplantation (LT), particularly in patients with hepatocellular carcinoma (HCC). We assessed current practices for HBV-R prophylaxis in Italy, evaluating rates, risk factors, and clinical impact of HBV-R a...
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Veröffentlicht in: | JHEP reports 2024-11, p.101278, Article 101278 |
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Zusammenfassung: | Conflicting data exist regarding optimal prophylaxis for HBV recurrence (HBV-R) after liver transplantation (LT), particularly in patients with hepatocellular carcinoma (HCC). We assessed current practices for HBV-R prophylaxis in Italy, evaluating rates, risk factors, and clinical impact of HBV-R and HCC-R.
Multicentric, retrospective study involving 20 Italian LT centers. All patients who underwent LT for HBV-related liver diseases between 2010 and 2021 were included. Logistic regression was used to identify predictors of HBV-R and HCC-R. Survival curves were estimated with Kaplan-Meier method and compared with log-rank test.
We included 1205 LT recipients (60.8% HCC). HBV prophylaxis was prescribed in 99.7% recipients, mostly with lifelong HBIG+NUCs (83.9%). Rates of HBV-R were 2.1% and 3.1% in patients transplanted without and with HCC, respectively. Median times from LT were 60 [9.5–77.5] and 5.5 [1–13] months, respectively. Recipients on lifelong HBIG+NUCs experienced lower rates of HBV-R than those in whom HBIG were withdrawn, used only during LT, or received NUCs alone (2.3% vs. 6.2% vs. 1.9% vs. 8%, respectively; p=0.042). In HCC recipients, HCC-R rate was 10.8% (median time from LT: 18 months). At multivariate analysis, HBV-R (OR: 10.329; 95%CI: 3.665-29.110), Child-Pugh C (OR: 3.519; 95%CI: 1.305-9.484), and microvascular invasion (OR: 3.088; 95%CI: 1.692-5.634) were independently associated with HCC-R. Five-year survival was lower in recipients who experienced HCC-R (32.5% vs. 92.4% in those who did not; p |
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ISSN: | 2589-5559 2589-5559 |
DOI: | 10.1016/j.jhepr.2024.101278 |