Browse > Article
http://dx.doi.org/10.3904/kjim.2015.30.2.170

Long-term virological outcome in chronic hepatitis B patients with a partial virological response to entecavir  

Jo, Yu Jung (Department of Internal Medicine, Inje University Ilsan Paik Hospital)
Kim, Kyung-Ah (Department of Internal Medicine, Inje University Ilsan Paik Hospital)
Lee, June Sung (Department of Internal Medicine, Inje University Ilsan Paik Hospital)
Kim, Nam-Hoon (Department of Internal Medicine, Inje University Ilsan Paik Hospital)
Bae, Won Ki (Department of Internal Medicine, Inje University Ilsan Paik Hospital)
Song, Tae June (Department of Internal Medicine, Inje University Ilsan Paik Hospital)
Kim, Jeong Wook (Department of Internal Medicine, Inje University Ilsan Paik Hospital)
Publication Information
The Korean journal of internal medicine / v.30, no.2, 2015 , pp. 170-176 More about this Journal
Abstract
Background/Aims: The clinical outcome of patients with a partial virological response (PVR) to entecavir (ETV), in particular nucloes(t)ide analogue (NA)-experienced patients, has not been thoroughly investigated. The aim of the present study was to assess long-term outcomes in NA-naive and NA-experienced chronic hepatitis B patients with a PVR to ETV. Methods: Chronic hepatitis B patients treated with ETV (0.5 mg/day) for at least 1 year were enrolled retrospectively. PVR was defined as a decrease in hepatitis B virus (HBV) DNA titer of more than $2log_{10}\;IU/mL$, yet with residual serum HBV DNA, as determined by real time-polymerase chain reaction, at week 48 of ETV therapy. Results: A total of 202 patients (127 NA-naive and 75 NA-experienced, male 70.8%, antigen positive 53.2%, baseline serum HBV DNA $6.2{\pm}1.5log_{10}\;IU/mL$) were analyzed. Twenty-eight patients demonstrated a PVR. The PVR was associated with a high serum HBV DNA titer at baseline and at week 24. Virological response (< 60 IU/mL) was achieved in 46.2%, 61.5%, 77.6%, and 85% of patients with PVR at week 72, 96, 144, and 192, respectively. Resistance to antivirals developed in two NA-experienced patients. Failure of virological response (VR) in patients with PVR was associated with high levels of serum HBV DNA at week 48. Conclusions: Patients with PVR to ETV had favorable long-term virological outcomes. The low serum level of HBV DNA (< 200 IU/mL) at week 48 was associated with subsequent development of a VR in patients with PVR to ETV.
Keywords
Hepatitis B, chronic; Entecavir; Partial virological response; Nucleos(t)ide analogue-experienced;
Citations & Related Records
Times Cited By KSCI : 1  (Citation Analysis)
연도 인용수 순위
1 Guo XF, Zhang CX, Liu Y, Wu F, Luo X. Drug-resistant genes at hepatitis B virus polymerase region during entecavir treatment. Zhongguo Yi Xue Ke Xue Yuan Xue Bao 2013;35:444-446.
2 Papatheodoridis G, Goulis J, Manolakopoulos S, et al. Changes of HBsAg and interferon-inducible protein 10 serum levels in naive HBeAg-negative chronic hepatitis B patients under 4-year entecavir therapy. J Hepatol 2014;60:62-68.   DOI   ScienceOn
3 Chang TT, Gish RG, de Man R, et al. A comparison of entecavir and lamivudine for HBeAg-positive chronic hepatitis B. N Engl J Med 2006;354:1001-1010.   DOI   ScienceOn
4 Lai CL, Shouval D, Lok AS, et al. Entecavir versus lamivudine for patients with HBeAg-negative chronic hepatitis B. N Engl J Med 2006;354:1011-1020.   DOI   ScienceOn
5 Chang TT, Lai CL, Kew Yoon S, et al. Entecavir treatment for up to 5 years in patients with hepatitis B e antigenpositive chronic hepatitis B. Hepatology 2010;51:422-430.   DOI   ScienceOn
6 Chang TT, Liaw YF, Wu SS, et al. Long-term entecavir therapy results in the reversal of fibrosis/cirrhosis and continued histological improvement in patients with chronic hepatitis B. Hepatology 2010;52:886-893.   DOI   ScienceOn
7 Hosaka T, Suzuki F, Kobayashi M, et al. Long-term entecavir treatment reduces hepatocellular carcinoma incidence in patients with hepatitis B virus infection. Hepatology 2013;58:98-107.
8 Papatheodoridis GV, Dimou E, Dimakopoulos K, et al. Outcome of hepatitis B e antigen-negative chronic hepatitis B on long-term nucleos(t)ide analog therapy starting with lamivudine. Hepatology 2005;42:121-129.
9 Zoulim F, Perrillo R. Hepatitis B: reflections on the current approach to antiviral therapy. J Hepatol 2008;48 Suppl 1:S2-S19.   DOI   ScienceOn
10 Lai CL, Gane E, Liaw YF, et al. Telbivudine versus lamivudine in patients with chronic hepatitis B. N Engl J Med 2007;357:2576-2588.   DOI   ScienceOn
11 Korean Association for the Study of the Liver. KASL Clinical Practice Guidelines: management of chronic hepatitis B. Clin Mol Hepatol 2012;18:109-162.   DOI
12 Yang SC, Lee CM, Hu TH, et al. Virological response to entecavir reduces the risk of liver disease progression in nucleos(t)ide analogue-experienced HBV-infected patients with prior resistant mutants. J Antimicrob Chemother 2013;68:2154-2163.   DOI   ScienceOn
13 Wang CC, Tseng TC, Wang PC, Lin HH, Kao JH. Baseline hepatitis B surface antigen quantitation can predict virologic response in entecavir-treated chronic hepatitis B patients. J Formos Med Assoc 2014;113:786-793.   DOI   ScienceOn
14 Zoutendijk R, Reijnders JG, Brown A, et al. Entecavir treatment for chronic hepatitis B: adaptation is not needed for the majority of naive patients with a partial virological response. Hepatology 2011;54:443-451.   DOI   ScienceOn
15 Bang SJ, Kim BG, Shin JW, et al. Clinical course of patients with insufficient viral suppression during entecavir therapy in genotype C chronic hepatitis B. Dig Liver Dis 2013;45:600-605.   DOI   ScienceOn
16 Liaw YF, Chu CM. Hepatitis B virus infection. Lancet 2009;373:582-592.   DOI   ScienceOn
17 Ko SY, Choe WH, Kwon SY, et al. Long-term impact of entecavir monotherapy in chronic hepatitis B patients with a partial virologic response to entecavir therapy. Scand J Gastroenterol 2012;47:1362-1367.   DOI   ScienceOn
18 Schiff ER, Lee SS, Chao YC, et al. Long-term treatment with entecavir induces reversal of advanced fibrosis or cirrhosis in patients with chronic hepatitis B. Clin Gastroenterol Hepatol 2011;9:274-276.   DOI   ScienceOn