Four years of lamivudine treatment in Chinese patients with chronic hepatitis B

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Názov: Four years of lamivudine treatment in Chinese patients with chronic hepatitis B
Autori: Chang, T.-T., Lai, C.-L., Chien, R.-N., Guan, R., Lim, S.-G., Lee, C.-M., Ng, K.-Y., Nicholls, G.J., Dent, J.C., Leung, N.W.Y.
Prispievatelia: MEDICINE
Zdroj: Journal of Gastroenterology and Hepatology. 19:1276-1282
Informácie o vydavateľovi: Wiley, 2004.
Rok vydania: 2004
Predmety: Asian Continental Ancestry Group, Adult, Male, Hepatitis B virus, Time Factors, Adolescent, Hepatitis B e Antigens - blood, Chronic hepatitis B, 03 medical and health sciences, Viral - blood, Hepatitis B, Chronic, 0302 clinical medicine, Asian People, Humans, Hepatitis B e Antigens, Hepatitis B Antibodies, Hepatitis B Surface Antigens - blood, Lamivudine - therapeutic use, Alanine Transaminase - blood, Chinese, Hepatitis B Surface Antigens, Chronic - blood - drug therapy, Alanine Transaminase, DNA, Hepatitis B Antibodies - blood, Middle Aged, Hepatitis B, Hepatitis B, Chronic - blood - drug therapy, Hepatitis B virus - genetics - immunology, 3. Good health, Treatment Outcome, Lamivudine, DNA, Viral, Reverse Transcriptase Inhibitors, Female, Reverse Transcriptase Inhibitors - therapeutic use, DNA, Viral - blood, Follow-Up Studies
Popis: Background and Aims: This study assessed the efficacy and safety of up to 4 years of lamivudine treatment and the clinical relevance of the emergence of YMDD‐variant hepatitis B virus (HBV).Methods: Fifty‐eight Chinese adult patients with chronic hepatitis B (CHB) were randomized to lamivudine 100 mg/day for up to 5 years and were monitored for YMDD‐variant HBV, hepatitis B e antigen (HBeAg) seroconversion (loss of HBeAg and detectable antibody to HBeAg) and serum alanine aminotransferase (ALT) concentrations. Four‐year data are reported here.Results: The rate of HBeAg seroconversion increased with extended therapy and also with higher baseline ALT concentrations. YMDD‐variant HBV was detected in 67% (39/58) of patients at some point during treatment. After 4 years, a total of 47% (27/58) of patients achieved HBeAg seroconversion. Thirty‐three per cent (13/39) of patients with YMDD‐variant HBV achieved HBeAg seroconversion; this increased to 57% (8/14) in patients with moderately elevated (>2–5 × upper limit of normal) pre‐treatment ALT concentrations. The proportion of patients that achieved normal serum ALT increased from 29% (17/58) at baseline to 69% (31/45) following 4 years of treatment. That included 68% (23/34) of patients with YMDD‐variant HBV and 73% (8/11) of those without the variant. All patients receiving lamivudine had reduced serum concentrations of HBV‐DNA compared with baseline, despite the emergence of YMDD‐variant HBV in 39 patients. Lamivudine was generally well tolerated; there was little change in the number or type of drug‐related adverse events in the fourth year of the study.Conclusions: Despite the emergence of YMDD‐variant HBV, Chinese patients showed increased HBeAg seroconversion and improvement in ALT levels with an increased duration of treatment with lamivudine.
Druh dokumentu: Article
Jazyk: English
ISSN: 1440-1746
0815-9319
DOI: 10.1111/j.1440-1746.2004.03428.x
Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/15482535
https://europepmc.org/article/MED/15482535
http://ir.lib.ncku.edu.tw/handle/987654321/78135
https://www.ncbi.nlm.nih.gov/pubmed/15482535
https://onlinelibrary.wiley.com/doi/10.1111/j.1440-1746.2004.03428.x/abstract
http://hub.hku.hk/handle/10722/76303
https://core.ac.uk/display/37907797
http://hdl.handle.net/10722/76303
Rights: Wiley Online Library User Agreement
Prístupové číslo: edsair.doi.dedup.....83cdacbfdf9638e3a6a7fd018a8d6a54
Databáza: OpenAIRE
Popis
Abstrakt:Background and Aims: This study assessed the efficacy and safety of up to 4 years of lamivudine treatment and the clinical relevance of the emergence of YMDD‐variant hepatitis B virus (HBV).Methods: Fifty‐eight Chinese adult patients with chronic hepatitis B (CHB) were randomized to lamivudine 100 mg/day for up to 5 years and were monitored for YMDD‐variant HBV, hepatitis B e antigen (HBeAg) seroconversion (loss of HBeAg and detectable antibody to HBeAg) and serum alanine aminotransferase (ALT) concentrations. Four‐year data are reported here.Results: The rate of HBeAg seroconversion increased with extended therapy and also with higher baseline ALT concentrations. YMDD‐variant HBV was detected in 67% (39/58) of patients at some point during treatment. After 4 years, a total of 47% (27/58) of patients achieved HBeAg seroconversion. Thirty‐three per cent (13/39) of patients with YMDD‐variant HBV achieved HBeAg seroconversion; this increased to 57% (8/14) in patients with moderately elevated (>2–5 × upper limit of normal) pre‐treatment ALT concentrations. The proportion of patients that achieved normal serum ALT increased from 29% (17/58) at baseline to 69% (31/45) following 4 years of treatment. That included 68% (23/34) of patients with YMDD‐variant HBV and 73% (8/11) of those without the variant. All patients receiving lamivudine had reduced serum concentrations of HBV‐DNA compared with baseline, despite the emergence of YMDD‐variant HBV in 39 patients. Lamivudine was generally well tolerated; there was little change in the number or type of drug‐related adverse events in the fourth year of the study.Conclusions: Despite the emergence of YMDD‐variant HBV, Chinese patients showed increased HBeAg seroconversion and improvement in ALT levels with an increased duration of treatment with lamivudine.
ISSN:14401746
08159319
DOI:10.1111/j.1440-1746.2004.03428.x