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Therapeutic effects of rituximab combined with cyclophosphamide on refractory idiopathic thrombocytopenic purpura

机译:利妥昔单抗联合环磷酰胺对难治性特发性血小板减少性紫癜的治疗作用

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摘要

Therapeutic effects of rituximab combined with cyclophosphamide on refractory idiopathic thrombocytopenic purpura (ITP) were investigated. We retrospectively analyzed 249 patients with refractory ITP who were admitted to Qingdao Hiser Medical Group between March 2013 and March 2017. Curative effects of patients treated with rituximab, cyclophosphamide, and combination therapy were observed and the changes of platelet count, PA IgG, and lymphocyte CD20 before and after treatment, as well as the incidence of adverse reactions after treatment, were compared. There was no significant difference in the expression of lymphocyte CD20, PA IgG and platelet count among the three groups of refractory ITP patients before treatment (P>0.05). After treatment, the expression levels of CD20 and PA IgG in lymphocytes were significantly downregulated, and platelet counts significantly increased in the three groups (P<0.05). After treatment, CD20 and PA IgG levels in combined therapy group were significantly lower, and platelet count was significantly higher, than those in the rituximab and cyclophosphamide groups (P<0.05). Also, after rituximab treatment, the expression levels of CD20 and PA IgG in lymphocytes were significantly lower than those in cyclophosphamide group (P<0.05), and platelet count was higher than that in cyclophosphamide group (P<0.05). After treatment, the total effective rate in combined therapy group was higher than that in the rituximab and cyclophosphamide group (P<0.05). Total effective rate of rituximab group was significantly higher than that of cyclophosphamide group (P<0.05). The incidence of adverse reactions in combined therapy group was 14.29% (12/84), which was significantly lower than that in cyclophosphamide group (40.70%, 35/86, P<0.05) and rituximab group (29.11%, 23/79, P<0.05). The application of rituximab combined with cyclophosphamide in the treatment of refractory ITP can improve patients clinical symptoms. The efficacy of this technique is promising with no serious adverse reactions. This technique should be popularized in clinical practice.
机译:研究了利妥昔单抗联合环磷酰胺对难治性特发性血小板减少性紫癜(ITP)的治疗作用。我们回顾性分析了2013年3月至2017年3月在青岛海斯医疗集团收治的249例难治性ITP患者。观察了利妥昔单抗,环磷酰胺和联合疗法治疗的患者的疗效,并观察了血小板计数,PA IgG和淋巴细胞的变化比较治疗前后的CD20以及治疗后不良反应的发生率。三组难治性ITP患者治疗前淋巴细胞CD20,PA IgG和血小板计数无明显差异(P> 0.05)。治疗后,三组淋巴细胞CD20和PA IgG的表达水平显着下调,血小板计数显着增加(P <0.05)。治疗后,联合治疗组的CD20和PA IgG水平明显低于利妥昔单抗和环磷酰胺组(P <0.05),血小板计数显着更高(P <0.05)。另外,利妥昔单抗治疗后,淋巴细胞中CD20和PA IgG的表达水平明显低于环磷酰胺组(P <0.05),血小板计数高于环磷酰胺组(P <0.05)。治疗后,联合治疗组的总有效率高于利妥昔单抗和环磷酰胺组(P <0.05)。利妥昔单抗组总有效率明显高于环磷酰胺组(P <0.05)。联合治疗组不良反应发生率为14.29%(12/84),明显低于环磷酰胺组(40.70%,35/86,P <0.05)和利妥昔单抗组(29.11%,23/79)。 P <0.05)。利妥昔单抗联合环磷酰胺在难治性ITP治疗中的应用可改善患者的临床症状。该技术的疗效令人期待,不会出现严重的不良反应。该技术应在临床实践中推广。

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