Pilot study of tenofovir disoproxil fumarate and pegylated interferon-alpha 2a add-on therapy in Japanese patients with chronic hepatitis B

被引:13
|
作者
Matsumoto, Akihiro [1 ]
Nishiguchi, Shuhei [2 ]
Enomoto, Hirayuki [2 ]
Tanaka, Yasuhito [3 ]
Shinkai, Noboru [3 ]
Okuse, Chiaki [4 ]
Kang, Jong-Hon [5 ]
Matsui, Takeshi [5 ]
Miyase, Shiho [6 ]
Yatsuhashi, Hiroshi [7 ]
Nagaoka, Shinya [7 ]
Kanda, Tatsuo [8 ]
Enomoto, Masaru [9 ]
Yamada, Ryoko [10 ]
Hiramatsu, Naoki [11 ]
Saito, Satoru [12 ]
Takaguchi, Koichi [13 ]
Ito, Kiyoaki [14 ]
Masaki, Tsutomu [15 ]
Morihara, Daisuke [16 ]
Tsuge, Masataka [17 ]
Chayama, Kazuaki [17 ]
Ikeda, Fusao [18 ]
Kagawa, Tatehiro [19 ]
Kondo, Yasuteru [20 ]
Murata, Kazumoto [21 ]
Tanaka, Eiji [22 ]
机构
[1] Shinshu Univ, Dept Med, Sch Med, Matsumoto, Nagano, Japan
[2] Hyogo Coll Med, Dept Internal Med, Div Hepatobiliary & Pancreat Dis, Nishinomiya, Hyogo, Japan
[3] Nagoya City Univ, Dept Virol & Liver Unit, Grad Sch Med Sci, Nagoya, Aichi, Japan
[4] Kawasaki Municipal Tama Hosp, Dept Internal Med, Div Gastroenterol & Hepatol, Kawasaki, Kanagawa, Japan
[5] Teine Keijinkai Hosp, Ctr Gastroenterol, Sapporo, Hokkaido, Japan
[6] Kumamoto Shinto Gen Hosp, Dept Gastroenterol & Hepatol, Kumamoto, Japan
[7] Natl Hosp Org Nagasaki Med Ctr, Clin Res Ctr, Omura, Japan
[8] Nihon Univ, Dept Med, Div Gastroenterol & Hepatol, Sch Med, Tokyo, Japan
[9] Osaka City Univ, Dept Hepatol, Med Sch, Osaka, Japan
[10] Osaka Univ Grad, Dept Gastroenterol & Hepatol, Sch Med, Osaka, Japan
[11] Osaka Rosai Hosp, Dept Gastroenterol, Sakai, Osaka, Japan
[12] Yokohama City Univ, Dept Gastroenterol & Hepatol, Sch Med, Yokohama, Kanagawa, Japan
[13] Kagawa Prefectural Cent Hosp, Dept Hepatol, Takamatsu, Kagawa, Japan
[14] Aichi Med Univ, Dept Internal Med, Div Hepatol & Pancreatol, Sch Med, Nagakute, Aichi, Japan
[15] Kagawa Univ, Dept Gastroenterol & Neurol, Sch Med, Takamatsu, Kagawa, Japan
[16] Fukuoka Univ, Dept Gastroenterol, Fac Med, Fukuoka, Japan
[17] Hiroshima Univ, Grad Sch Biomed & Hlth Sci, Dept Gastroenterol & Metab, Hiroshima, Japan
[18] Okayama Univ, Dept Gastroenterol & Hepatol, Grad Sch Med Dent & Pharmaceut Sci, Okayama, Japan
[19] Tokai Univ, Dept Internal Med, Div Gastroenterol, Sch Med, Isehara, Kanagawa, Japan
[20] Sendai Kousei Hosp, Dept Hepatol, Sendai, Miyagi, Japan
[21] Jichi Med Univ, Dept Infect & Immun, Div Virol, Sch Med, Shimotsuke, Tochigi, Japan
[22] Shinshu Univ, Sch Med, Dept Promot Reg Med, Asahi 3-1-1, Matsumoto, Nagano 3908621, Japan
关键词
Hepatitis B surface antigen; Hepatitis B core-related antigen; Pegylated interferon; Tenofovir; Add-on therapy; NUCLEOS(T)IDE ANALOG THERAPY; CORE-RELATED ANTIGEN; HEPATOCELLULAR-CARCINOMA; SEQUENTIAL TREATMENT; SURFACE-ANTIGEN; VIRUS INFECTION; LAMIVUDINE; ENTECAVIR; MONOTHERAPIES; COMBINATION;
D O I
10.1007/s00535-020-01707-6
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background A prospective pilot study of tenofovir disoproxil fumarate (TDF) and pegylated interferon alpha 2a (P-IFN) add-on therapy was conducted to evaluate its efficacy in reducing viral antigen levels in Japanese patients with chronic hepatitis B (UMIN 000020179). Methods Patients with chronic hepatitis B receiving maintenance TDF therapy and exhibiting hepatitis B surface antigen (HBsAg) level > 800 IU/ml were divided into two arms. P-IFN was added for 48 weeks in the add-on arm (n = 32), while TDF monotherapy was maintained in the control arm (n = 51). Both groups were followed for 96 weeks after baseline measurements. Results Almost all patients in the control arm displayed a slow and constant reduction in HBsAg during follow-up. In contrast, roughly half of the add-on arm exhibited a sharp decline in HBsAg during P-IFN administration, which disappeared after halting P-IFN. At 96 weeks after baseline, 41% (13/32) of patients in the add-on arm had shown a rapid decrease in HBsAg, versus 2% (1/51) in the control arm (p < 0.001). Add-on therapy and increased cytotoxic T-cell response were significant factors associated with a rapid decrease in HBsAg according to multivariate analysis. In addition, higher HB core-related antigen (HBcrAg) level at baseline (p = 0.001) and add-on therapy (p = 0.036) were significant factors associated with a rapid reduction in HBcrAg. Conclusions TDF and P-IFN add-on therapy in Japanese patients with chronic hepatitis B facilitated rapid decreases in HBsAg and HBcrAg. Further studies are needed to improve early HBsAg clearance rate.
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收藏
页码:977 / 989
页数:13
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