Add-on Pegylated Interferon Alpha-2a Therapy in Chronic Hepatitis B Japanese Patients Treated with Entecavir
Author(s) -
Hideyuki Tamai,
Yoshiyuki Ida,
Naoki Shingaki,
Ryo Shimizu,
Kazuhiro Fukatsu,
Masahiro Itonaga,
Takeichi Yoshida,
Yoshimasa Maeda,
Kosaku Moribata,
Takao Maekita,
Mikitaka Iguchi,
Jun Kato,
Masayuki Kitano
Publication year - 2017
Publication title -
hepatitis research and treatment
Language(s) - English
Resource type - Journals
eISSN - 2090-1372
pISSN - 2090-1364
DOI - 10.1155/2017/2093847
Subject(s) - entecavir , medicine , pegylated interferon , chronic hepatitis , virology , alpha (finance) , hepatitis b , gastroenterology , surgery , virus , lamivudine , ribavirin , construct validity , patient satisfaction
Entecavir requires long-term administration. Pegylated interferon (PEG-IFN) therapy leads to significant reduction of hepatitis B surface antigen (HBs Ag) levels. This study aimed to assess the safety and efficacy of adding PEG-IFN- α -2a to entecavir toward cessation of entecavir. A total of 23 patients treated with entecavir underwent add-on PEG-IFN- α -2a therapy (90 μ g per week) for 48 weeks. Viral response (VR) was defined as more than 50% reduction of baseline hepatitis B surface antigen (HBs Ag) level at 72 weeks from the start of therapy. Complete response (CR) was defined as the decline of HBs Ag levels <100 IU/mL. Hepatitis B e antigen (HBe Ag) seroconversion rate was 25% (2/8), and VR rate was 52% (12/23). CR was observed in four patients (17%). However, CR rate in baseline HBs Ag level <2000 IU/mL and HBe Ag negative patients was 50% (4/8). Univariate analysis showed that the percentage of HBs Ag level reduction at week 12 was significantly associated with VR. The area under the curve value was 0.848. Adding PEG-IFN- α -2a to entecavir has limited efficacy. The percentage reduction of HBs Ag level at week 12 may be a useful predictor for VR.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom