Double filtration plasmapheresis and interferon combination therapy for chronic hepatitis C patients with genotype 1 and high viral load

被引:34
作者
Fujiwara, Kenji
Kaneko, Shuichi
Kakumu, Shinichi
Sata, Michio
Hige, Shuhei
Tomita, Eiichi
Mochida, Satoshi
机构
[1] Kanazawa Univ, Grad Sch Med, Dept Gastroenterol, Kanazawa, Ishikawa 9208640, Japan
[2] Yokohama Rosai Hosp, Yokohama, Kanagawa, Japan
[3] Aichi Med Univ, Nagakute, Aichi 48011, Japan
[4] Kurume Univ, Sch Med, Kurume, Fukuoka 830, Japan
[5] Hokkaido Univ, Grad Sch Med, Sapporo, Hokkaido, Japan
[6] Gifu Municipal Hosp, Gifu, Japan
[7] Saitama Med Univ, Moroyama, Saitama, Japan
关键词
combination therapy; double filtration plasmapheresis; early viral reduction; non-responder; relapser; sustained virus response;
D O I
10.1111/j.1872-034X.2007.00117.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The efficacy and safety of double filtration plasmapheresis (DFPP) plus interferon (IFN) combination therapy were compared with those of IFN therapy alone in 193 chronic hepatitis C patients having a high hepatitis C virus ribonucleic acid load of difficult-to-treat genotype 1b. All patients received either interferon alpha-2b (IFN-alpha-2b) monotherapy or combination therapies with ribavirin and IFN-alpha-2b or pegylated interferon alpha-2b (PEG-IFN-alpha-2b). Each patient individually decided whether to receive concomitant DFPP. DFPP was immediately followed by IFN treatment, and up to five sessions were given during the first week. Sixty patients decided to receive DFPP. In the DFPP plus PEG-IFN-alpha-2b therapy group (n = 30), viral load reduction at 4 weeks after the start of treatment was greater than innon-DFPP (n = 74) (2.47 vs 1.52, log, P = 0.010), and the sustained virus response was also higher (77.8% vs 50.0%), even in cases of re-treated patients (relapsers or non-responders to previous IFN therapies). Adverse events, mild and transient, were observed in 38.3% of all DFPP-treated patients. DFPP plus IFN combination therapy produced a great reduction of viral load during the early stage of treatment and achieved a high sustained virus response, suggesting that this combination therapy may be a new modality for chronic hepatitis C patients at difficult-to-treat states.
引用
收藏
页码:701 / 710
页数:10
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