HBV DNA suppression and HBsAg clearance in HBeAg negative chronic hepatitis B patients on lamivudine therapy for over 5 years

被引:48
作者
Fasano, Massimo [2 ,8 ]
Lampertico, Pietro [3 ]
Marzano, Alfredo [4 ]
Di Marco, Vito [5 ]
Niro, Grazia Anna [6 ]
Brancaccio, Giuseppina [7 ]
Marengo, Andrea [4 ]
Scotto, Gaetano
Brunetto, Maurizia Rossana [1 ]
Gaeta, Giovanni Battista [7 ]
Rizzetto, Mario [4 ]
Angarano, Gioacchino [2 ,8 ]
Santantonio, Teresa
机构
[1] Univ Hosp Pisa, Hepatol Unit, Pisa, Italy
[2] Univ Bari, Clin Infect Dis, Bari, Italy
[3] Univ Milan, Dept Med, Div Gastroenterol 1, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Milan, Italy
[4] AOU San Giovanni Battista, Gastrohepatol Unit, Turin, Italy
[5] Univ Palermo, Gastroenterol & Hepatol Unit, Dept Internal Med, Palermo, Italy
[6] IRCCS Casa Sollievo Sofferenza, Gastroenterol Unit, San Giovanni Rotondo, Italy
[7] Univ Naples 2, Clin Infect Dis, Naples, Italy
[8] Univ Foggia, Clin Infect Dis, I-71100 Foggia, Italy
关键词
Nucleos(t)ide analogues; Lamivudine; Viral resistance; Chronic hepatitis B; SURFACE-ANTIGEN; SERUM HBSAG; LONG-TERM; VIROLOGICAL RESPONSE; ALPHA-2A;
D O I
10.1016/j.jhep.2012.01.022
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: In long-term responder patients, it is unclear whether lamivudine (LAM) monotherapy should be continued or switched to a high-genetic-barrier analogue. This study aims at assessing LAM efficacy over a 5-year period and the residual risk of drug resistance. The rate of HBsAg clearance and LAM long-term safety profile were also evaluated. Methods: One hundred and ninety-one patients with chronic HBeAg-negative hepatitis B successfully treated with LAM monotherapy for at least 5-years were included. Biochemical and virological tests were assessed every 3 months in all patients and HBsAg quantification was performed in 45/191. Reverse-transcriptase (RT) region was directly sequenced in virological breakthrough patients. Results: One hundred and ninety-one patients (148 males, median age 53 years, 72 with compensated cirrhosis) responding to 60-month LAM monotherapy continued to receive LAM monotherapy beyond the initial 5 years and were followed for an additional 36-month median period (range 1-108). Virological response was maintained in 128/191 patients (67%) and HBsAg clearance was observed in 15/128 (11.7%) after a 32-month median period (range 1-65). The 63 remaining patients (33%) showed virological breakthrough after a 15-month median treatment (range 1-78). RT region analysis was performed in 38/63 breakthrough patients and LAM resistant mutations were found in 37/38. No significant side effects were observed. Conclusions: In long-term responder patients, continuation of LAM monotherapy resulted in persistent viral suppression in most cases with undetectable HBV DNA by real-time PCR; moreover, 11.7% of these patients cleared HBsAg. Selection of LAM resistance, however, can still occur even after successful long-term therapy, thus emphasising the importance of a careful virological monitoring. (C) 2012 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1254 / 1258
页数:5
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