Predicting relapse after cessation of lamivudine monotherapy for chronic hepatitis B virus infection

被引:18
作者
Ito, K
Tanaka, Y
Orito, E
Hirashima, N
Ide, T
Hino, T
Kumashiro, R
Kato, A
Nukaya, H
Sakakibara, K
Mukaide, M
Ito, H
Sata, M
Ueda, R
Mizokami, M [1 ]
机构
[1] Nagoya City Univ, Grad Sch Med Sci, Dept Clin Mol Informat Med, Mizuho Ku, Nagoya, Aichi 4678601, Japan
[2] Nagoya City Univ, Grad Sch Med Sci, Chukyo Hosp, Dept Gastroenterol,Mizuho Ku, Nagoya, Aichi 4678601, Japan
[3] Nagoya City Univ, Grad Sch Med Sci, Dept Internal Med & Mol Sci, Mizuho Ku, Nagoya, Aichi 4678601, Japan
[4] Aichi Canc Ctr, Res Inst, Div Epidemiol & Prevent, Nagoya, Aichi 464, Japan
[5] Kurume Univ, Sch Med, Dept Internal Med 2, Kurume, Fukuoka 830, Japan
[6] SRL Inc, Tokyo, Japan
关键词
D O I
10.1086/380965
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
There have been reports of relapse after cessation of lamivudine monotherapy for hepatitis B virus (HBV) infection. The aim of this study was to examine factors that predict posttreatment relapse. Comparison 22 patients who experienced relapse with 11 who did not after cessation of therapy showed that predictive factors for nonrelapse were hepatitis B e antigen seroconversion and duration of undetectable HBV DNA load (<0.7 log IU/mL), as determined by HBV real-time detection direct testing. However, 7 of 12 patients with seroconversion experienced relapse after cessation of therapy. Multivariate analysis revealed that the duration of an undetectable HBV DNA load was the only independent predictive factor for nonrelapse (odds ratio, 0.50; 95% confidence interval, 0.27-0.9). More-prolonged lamivudine therapy is required after seroconversion, and persistent duration of an HBV DNA level of <0.7 log IU/mL for >6 months can more accurately aid in the decision of when to stop lamivudine therapy.
引用
收藏
页码:490 / 495
页数:6
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