Sporea Ioan, Popescu Alina, Sirli Roxana, Golea Ovidiu, Totolici Camelia, Danila Mirela, Vernic Corina
University of Medicine and Pharmacy, Department of Gastroenterology, Timisoara, Romania.
World J Gastroenterol. 2006 Jul 14;12(26):4191-4. doi: 10.3748/wjg.v12.i26.4191.
To evaluate the response to pegylated-interferon alpha 2a in chronic hepatitis C patients on chronic haemodialysis.
Ten patients with chronic C hepatitis were enrolled in this study. All had increased aminotransferases for more than 6 mo, positive antiHCV antibodies and positive PCR HCV-RNA. We administrated Peg-Interferon alpha 2a 180 microg/wk for 48 wk. After 12 wk of treatment we evaluated the biochemical and early virological response (EVR). At the end of the treatment we evaluated the biochemical response and 24 wk after the end of the treatment we evaluated the sustained virological response (SVR). We monitored the side-effects during the treatment.
Two patients dropped out in the first 12 wk of treatment and 2 after the first 12 wk of treatment. After 12 wk of treatment, 7 out of 8 patients had biochemical response and EVR and 1 had biochemical response but persistent viremia. We had to reduce the dose of pegylated-interferon to 135 mug/wk in 2 cases. Three out of 6 (50%) patients had SVR 24 wk after the end of the treatment. Intention-to-treat analysis showed that 3 out of 10 patients (30%) had SVR. Side-effects occurred in most of the patients (flu-like syndrome, thrombocytopenia or leucopoenia), but they did not impose the discontinuation of treatment.
After 12 wk of treatment with Peg-Interferon alpha 2a (40 ku) in patients on chronic haemodialysis with chronic C hepatitis, EVR was obtained in 87.5% (7/8) of the cases. SVR was achieved in 50% of the cases (3/6 patients) that finished the 48 wk of treatment.
评估聚乙二醇化干扰素α-2a对慢性血液透析的丙型肝炎患者的疗效。
本研究纳入10例慢性丙型肝炎患者。所有患者转氨酶升高超过6个月,抗HCV抗体阳性且PCR HCV-RNA阳性。我们给予聚乙二醇干扰素α-2a 180μg/周,共48周。治疗12周后,我们评估生化和早期病毒学应答(EVR)。治疗结束时,我们评估生化应答,治疗结束24周后,我们评估持续病毒学应答(SVR)。我们在治疗期间监测副作用。
2例患者在治疗的前12周退出,2例在治疗的前12周后退出。治疗12周后,8例患者中有7例有生化应答和EVR,1例有生化应答但病毒血症持续存在。2例患者我们不得不将聚乙二醇化干扰素的剂量减至135μg/周。治疗结束24周后,6例患者中有3例(50%)有SVR。意向性分析显示,10例患者中有3例(30%)有SVR。大多数患者出现副作用(流感样综合征、血小板减少或白细胞减少),但未导致治疗中断。
在慢性血液透析的慢性丙型肝炎患者中,用聚乙二醇干扰素α-2a(40ku)治疗12周后,87.5%(7/8)的病例获得EVR。完成48周治疗的病例中有50%(3/6例患者)实现了SVR。