Osborn Melissa K, Han Steven H, Regev Arie, Bzowej Natalie H, Ishitani Michael B, Tran Tram T, Lok Anna S F
University of Michigan Medical Center, Ann Arbor, Michigan 48109, USA.
Clin Gastroenterol Hepatol. 2007 Dec;5(12):1454-61. doi: 10.1016/j.cgh.2007.08.008. Epub 2007 Oct 31.
BACKGROUND & AIMS: Lamivudine has been shown to improve liver disease and survival of hepatitis B virus patients on the orthotopic liver transplantation (OLT) waiting list, but liver failure might worsen in patients with drug resistance. Use of antiviral salvage therapy might decrease this risk.
We analyzed data from patients enrolled in the NIH HBV OLT cohort to study the effects of pretransplant antiviral therapy on transplant-free survival and survival without transplant. We also compared the clinical outcomes of those who did or did not develop antiviral failure (virologic breakthrough or genotypic resistance) while awaiting transplant.
One hundred twenty-two eligible patients received antiviral therapy before OLT and were followed for a median of 40.5 months (range, 0.4-123.0 months) after initiation of antiviral therapy. Forty-four (36.1%) patients developed antiviral failure; all had lamivudine monotherapy as initial treatment. Forty-two patients started salvage therapy a median of 5 months after lamivudine failure; the median Model for End-Stage Liver Disease (MELD) score was 12. Twenty-one (50%) patients had a full response to salvage therapy. Eleven (26.2%) patients had a suboptimal virologic response but remained clinically compensated. Antiviral failure was not a significant predictor of transplant or death (P = .09) or death without transplant (P = .39). Multivariate predictors of transplant or death were high MELD score, hepatocellular carcinoma, and low albumin. High MELD score and low albumin were predictors of death without transplant.
Antiviral failure in patients with HBV on the OLT waiting list did not impair clinical outcome if recognized early and if salvage therapy is promptly initiated.
已证实拉米夫定可改善乙型肝炎病毒患者在原位肝移植(OLT)等待名单上的肝病状况及生存率,但耐药患者的肝衰竭可能会恶化。使用抗病毒挽救疗法可能会降低这种风险。
我们分析了参与美国国立卫生研究院(NIH)HBV OLT队列研究的患者数据,以研究移植前抗病毒治疗对无移植生存和非移植生存的影响。我们还比较了等待移植期间出现或未出现抗病毒治疗失败(病毒学突破或基因型耐药)患者的临床结局。
122例符合条件的患者在OLT前接受了抗病毒治疗,抗病毒治疗开始后中位随访40.5个月(范围0.4 - 123.0个月)。44例(36.1%)患者出现抗病毒治疗失败;所有患者最初均接受拉米夫定单药治疗。42例患者在拉米夫定治疗失败后中位5个月开始挽救治疗;终末期肝病模型(MELD)评分中位数为12。21例(50%)患者对挽救治疗有完全反应。11例(26.2%)患者病毒学反应欠佳但临床仍保持代偿。抗病毒治疗失败并非移植或死亡(P = 0.09)或非移植死亡(P = 0.39)的显著预测因素。移植或死亡的多因素预测因素为高MELD评分、肝细胞癌和低白蛋白。高MELD评分和低白蛋白是非移植死亡的预测因素。
OLT等待名单上的HBV患者若早期发现抗病毒治疗失败并及时启动挽救治疗,临床结局不会受到影响。