Efficacy of Entecavir in Chronic Hepatitis B Patients with Mildly Elevated Alanine Aminotransferase and Biopsy-Proven Histological Damage

被引:44
|
作者
Wu, I-Chin [2 ]
Lai, Ching-Lung [3 ]
Han, Steven-Huy Bui [4 ]
Han, Kwang-Hyup [5 ]
Gordon, Stuart C. [6 ]
Chao, You-Chen [7 ]
Tan, Chee-Kiat [8 ]
Sievert, William [9 ]
Tanwandee, Tawesak [10 ]
Xu, Dong [11 ]
Neo, Boon-Leong [12 ]
Chang, Ting-Tsung [1 ,2 ]
机构
[1] Natl Cheng Kung Univ Hosp, Dept Internal Med, Tainan 704, Taiwan
[2] Natl Cheng Kung Univ, Coll Med, Inst Clin Med, Tainan 70101, Taiwan
[3] Univ Hong Kong, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China
[4] Univ Calif Los Angeles, Sch Med, Los Angeles, CA USA
[5] Yonsei Univ, Coll Med, Severance Hosp, Seoul, South Korea
[6] Henry Ford Hosp, Detroit, MI 48202 USA
[7] Tri Serv Gen Hosp, Taipei, Taiwan
[8] Singapore Gen Hosp, Singapore 0316, Singapore
[9] Monash Univ, Dept Med, Monash Med Ctr, Melbourne, Vic 3004, Australia
[10] Siriraj Hosp, Bangkok, Thailand
[11] Bristol Myers Squibb Co, Res & Dev, Wallingford, CT 06492 USA
[12] Bristol Myers Squibb Co, Res & Dev, Singapore, Singapore
关键词
NATURAL-HISTORY; VIRUS INFECTION; LAMIVUDINE; MANAGEMENT; DISEASE;
D O I
10.1002/hep.23424
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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 X 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 x ULN. To assess therapeutic efficacy in this clinical setting, we retrospectively examined treatment endpoints among the subset of nucleoside-naive 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 x 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 x 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 HBeAg-negative 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 x ULN. However, entecavir-treated HBeAg-positive patients with mildly elevated ALT had lower response rates for histological improvement, HBV DNA less than 300 copies/mL, ALT normalization, and HBeAg seroconversion than those with ALT greater than 2 X ULN. Conclusion: This retrospective analysis demonstrated that HBeAg-negative CHB 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 x ULN. (HEPATOLOGY 2010;51:1185-1189.)
引用
收藏
页码:1185 / 1189
页数:5
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