首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Rituximab plus Peg-interferon-alpha/ribavirin compared with Peg-interferon-alpha/ribavirin in hepatitis C-related mixed cryoglobulinemia.
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Rituximab plus Peg-interferon-alpha/ribavirin compared with Peg-interferon-alpha/ribavirin in hepatitis C-related mixed cryoglobulinemia.

机译:Rituximab加上PEG-干扰素-α/利巴韦林与甲型肝炎相关混合冷冻蛋白血症中的PEG-干扰素-α/利巴韦林相比。

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摘要

Treatment of hepatitis C (HCV)-mixed cryoglobulinemia (MC) may target either the viral trigger (HCV) or the downstream B-cell clonal expansion. Prospective cohort study of 38 HCV-MC patients who received a combination of rituximab (375 mg/m(2)) once a week for 1 month followed by Peg-interferon-alpha (Peg-IFN-alpha; 2a, 180 microg or 2b, 1.5 microg/kg) weekly plus ribavirin (600-1200 mg) daily for 48 weeks were compared with 55 HCV-MC patients treated by Peg-IFN-alpha/ribavirin with the same modalities. In the whole population of HCV-MC patients (n = 93), a complete clinical response was achieved in 73.1% (68 of 93), cryoglobulin clearance in 52.7% (49 of 93), and a sustained virologic response in 59.1% (55 of 93). Compared with Peg-IFN-alpha/ribavirin, rituximab plus Peg-IFN-alpha/ribavirin-treated patients had a shorter time to clinical remission (5.4 +/- 4 vs 8.4 +/- 4.7 months, P = .004), better renal response rates (80.9% vs 40% of complete response, P = .040), and higher rates of cryoglobulin clearance (68.4% vs 43.6%, P = .001) and clonal VH1-69(+) B-cell suppression (P < .01). Treatment was well tolerated with 11% of discontinuation resulting from antiviral therapy and no worsening of HCV RNA under rituximab. Our findings indicate that rituximab combined with Peg-IFN-alpha/ribavirin is well tolerated and more effective than Peg-IFN-alpha/ribavirin in HCV-MC.
机译:治疗丙型肝炎(HCV) - 混合冷冻蛋白酶(MC)可以靶向病毒触发(HCV)或下游B细胞克隆膨胀。预期队列综合研究38个HCV-MC-MC患者,接受Rituximab(375mg / m(2))的组合,每周1个月,其次是PEG-干扰素-α(PEG-IFN-alpha; 2a,180 microg或2b 1.5 microg / kg)每周加上利韦韦林(600-1200mg)每日48周,与PEG-IFN-α/利巴韦林具有相同模式处理的55例HCV-MC-MC患者。在HCV-MC患者(N = 93)的整个人口中,在73.1%(93个)中实现了完整的临床反应,在52.7%(93个中的49个)中的冷冻胶蛋白清除和59.1%( 55 of 93)。与PEG-IFN-α/利巴韦林相比,Rituximab Plus PEG-IFN-α/利巴韦林治疗的患者的临床缓解时间较短(5.4 +/- 4 Vs 8.4 +/- 4.7个月,P = .004),更好肾脏反应率(80.9%与完全响应的40%,p = .040),低温胶质蛋白清除率较高(68.4%vs 43.6%,p = .001)和克隆VH1-69(+)B细胞抑制( p <.01)。用抗病毒治疗产生11%的停药性耐受良好的耐受性,并且在Rituximab下没有恶化HCV RNA。我们的研究结果表明,Rituximab与PEG-IFN-α/利巴韦林相结合,其在HCV-MC中的PEG-IFN-α/利巴韦林具有良好的耐受性和更有效。

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