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- Publisher Website: 10.1002/hep.23424
- Scopus: eid_2-s2.0-77950609092
- PMID: 20044806
- WOS: WOS:000276538100014
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Article: Efficacy of entecavir in chronic hepatitis b patients with mildly elevated alanine aminotransferase and biopsy-proven histological damage
Title | Efficacy of entecavir in chronic hepatitis b patients with mildly elevated alanine aminotransferase and biopsy-proven histological damage |
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Authors | |
Issue Date | 2010 |
Publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www.hepatology.org/ |
Citation | Hepatology, 2010, v. 51 n. 4, p. 1185-1189 How to Cite? |
Abstract | Current guidelines for management of chronic hepatitis B recommend treatment for patients presenting with elevated hepatitis B virus (HBV) DNA and alanine aminotransferase (ALT) >2 × upper limit of normal (ULN) or histological evidence of liver disease. Retrospective analyses have demonstrated that significant hepatic necroinflammation and fibrosis were present in a substantial proportion of patients with ALT 1 to 2×ULN. To assess therapeutic efficacy in this clinical setting, we retrospectively examined treatment endpoints among the subset of nucleoside-naïve chronic hepatitis B (CHB) patients treated in phase 3 clinical trials of entecavir who had both screening and baseline serum ALT 1.3 to 2×ULN. A total of 1347 patients were randomized to treatment with entecavir or lamivudine. Three hundred thirty-six patients, constituting 25% of the total study population, had screening and baseline ALT 1.3 to 2 × ULN. Clinically significant necroinflammation (Knodell necroinflammation score >7) was observed in 60% and 72% of hepatitis B e antigen (HBeAg)-positive and HBeAg-negative patients, respectively, whereas marked fibrosis (Ishak fibrosis score >4) was observed in 8% and 15% of HBeAg-positive and HBeAg-negative patients, respectively. Among entecavir-treated HBeAgnegative patients, the proportions of patients achieving histological improvement, HBV DNA <300 copies/mL, and ALT normalization were similar between patients with mildly elevated ALT and those with ALT>2×ULN. However, entecavir-treated HBeAg-positive patients with mildly elevated ALT had lower response rates for histological improvement,HBVDNAless than 300 copies/mL, ALT normalization, and HBeAg seroconversion than those with ALT greater than 2×ULN. Conclusion: This retrospective analysis demonstrated that HBeAg-negativeCHB patients treated with entecavir responded similarly irrespective of baseline ALT level. However, HBeAg-positive patients with mildly elevated ALT responded less well to treatment with entecavir than did those with ALT greater than 2 × ULN. Copyright © 2010 by the American Association for the Study of Liver Diseases. |
Persistent Identifier | http://hdl.handle.net/10722/163302 |
ISSN | 2023 Impact Factor: 12.9 2023 SCImago Journal Rankings: 5.011 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wu, IC | en_US |
dc.contributor.author | Lai, CL | en_US |
dc.contributor.author | Bui Han, SH | en_US |
dc.contributor.author | Han, KH | en_US |
dc.contributor.author | Gordon, SC | en_US |
dc.contributor.author | Chao, YC | en_US |
dc.contributor.author | Tan, CK | en_US |
dc.contributor.author | Sievert, W | en_US |
dc.contributor.author | Tanwandee, T | en_US |
dc.contributor.author | Xu, D | en_US |
dc.contributor.author | Neo, BL | en_US |
dc.contributor.author | Chang, TT | en_US |
dc.date.accessioned | 2012-09-05T05:29:51Z | - |
dc.date.available | 2012-09-05T05:29:51Z | - |
dc.date.issued | 2010 | en_US |
dc.identifier.citation | Hepatology, 2010, v. 51 n. 4, p. 1185-1189 | en_US |
dc.identifier.issn | 0270-9139 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/163302 | - |
dc.description.abstract | Current guidelines for management of chronic hepatitis B recommend treatment for patients presenting with elevated hepatitis B virus (HBV) DNA and alanine aminotransferase (ALT) >2 × upper limit of normal (ULN) or histological evidence of liver disease. Retrospective analyses have demonstrated that significant hepatic necroinflammation and fibrosis were present in a substantial proportion of patients with ALT 1 to 2×ULN. To assess therapeutic efficacy in this clinical setting, we retrospectively examined treatment endpoints among the subset of nucleoside-naïve chronic hepatitis B (CHB) patients treated in phase 3 clinical trials of entecavir who had both screening and baseline serum ALT 1.3 to 2×ULN. A total of 1347 patients were randomized to treatment with entecavir or lamivudine. Three hundred thirty-six patients, constituting 25% of the total study population, had screening and baseline ALT 1.3 to 2 × ULN. Clinically significant necroinflammation (Knodell necroinflammation score >7) was observed in 60% and 72% of hepatitis B e antigen (HBeAg)-positive and HBeAg-negative patients, respectively, whereas marked fibrosis (Ishak fibrosis score >4) was observed in 8% and 15% of HBeAg-positive and HBeAg-negative patients, respectively. Among entecavir-treated HBeAgnegative patients, the proportions of patients achieving histological improvement, HBV DNA <300 copies/mL, and ALT normalization were similar between patients with mildly elevated ALT and those with ALT>2×ULN. However, entecavir-treated HBeAg-positive patients with mildly elevated ALT had lower response rates for histological improvement,HBVDNAless than 300 copies/mL, ALT normalization, and HBeAg seroconversion than those with ALT greater than 2×ULN. Conclusion: This retrospective analysis demonstrated that HBeAg-negativeCHB patients treated with entecavir responded similarly irrespective of baseline ALT level. However, HBeAg-positive patients with mildly elevated ALT responded less well to treatment with entecavir than did those with ALT greater than 2 × ULN. Copyright © 2010 by the American Association for the Study of Liver Diseases. | en_US |
dc.language | eng | en_US |
dc.publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www.hepatology.org/ | en_US |
dc.relation.ispartof | Hepatology | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Alanine Transaminase - Blood | en_US |
dc.subject.mesh | Antiviral Agents - Therapeutic Use | en_US |
dc.subject.mesh | Biopsy | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Guanine - Analogs & Derivatives - Therapeutic Use | en_US |
dc.subject.mesh | Hepatitis B E Antigens - Analysis | en_US |
dc.subject.mesh | Hepatitis B, Chronic - Drug Therapy - Physiopathology | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Liver - Physiopathology | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Retrospective Studies | en_US |
dc.title | Efficacy of entecavir in chronic hepatitis b patients with mildly elevated alanine aminotransferase and biopsy-proven histological damage | en_US |
dc.type | Article | en_US |
dc.identifier.email | Lai, CL:hrmelcl@hku.hk | en_US |
dc.identifier.authority | Lai, CL=rp00314 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1002/hep.23424 | en_US |
dc.identifier.pmid | 20044806 | - |
dc.identifier.scopus | eid_2-s2.0-77950609092 | en_US |
dc.identifier.hkuros | 181153 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-77950609092&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 51 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.spage | 1185 | en_US |
dc.identifier.epage | 1189 | en_US |
dc.identifier.isi | WOS:000276538100014 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Wu, IC=15128207400 | en_US |
dc.identifier.scopusauthorid | Lai, CL=7403086396 | en_US |
dc.identifier.scopusauthorid | Bui Han, SH=6504060721 | en_US |
dc.identifier.scopusauthorid | Han, KH=7402963689 | en_US |
dc.identifier.scopusauthorid | Gordon, SC=7401828663 | en_US |
dc.identifier.scopusauthorid | Chao, YC=23117629900 | en_US |
dc.identifier.scopusauthorid | Tan, CK=15768583000 | en_US |
dc.identifier.scopusauthorid | Sievert, W=7004049384 | en_US |
dc.identifier.scopusauthorid | Tanwandee, T=7801658735 | en_US |
dc.identifier.scopusauthorid | Xu, D=15761595300 | en_US |
dc.identifier.scopusauthorid | Neo, BL=26653618800 | en_US |
dc.identifier.scopusauthorid | Chang, TT=7404725147 | en_US |
dc.identifier.issnl | 0270-9139 | - |