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首页> 外文期刊>National Journal of Medical Research >2 Years Effectiveness of Rituximab in Refractory Idiopathic Thrombocytopenic Purpura
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2 Years Effectiveness of Rituximab in Refractory Idiopathic Thrombocytopenic Purpura

机译:利妥昔单抗治疗难治性特发性血小板减少性紫癜的2年疗效

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Background and aim: The treatment of immune thrombocytopenia (ITP) started with steroids but most patients will relapse or have significant adverse effects. The use of Rituximab was greeted enthusiastically: it led to up to 60% response rates, making it the main alternative to splenectomy, with far fewer side effects. The aim of study to assess the 2 years effectiveness of rituximab in the managements of patients with chronic and refractory immune thrombocytopenic purpura (ITP). Methods and Materials: Retrospective study included 22 patients labeled as refractory chronic idiopathic thrombocytopenic purpura (ITP), This study was conducted at King Hussein Medical center / Amman -Jordan, Hematology and Oncology Department between February 2017 and February 2019, a weekly 4 doses of Rituximab 375mg/m2 were given, a 2 years regular follow up on the efficacy and safety of rituximab were identified. Results: The mean age at diagnosis was 36.7 years (19-54), Mean platelet count before rituximab treatment was 8×109 /L.All patients were followed for 2 years , the overall response rate to rituximab was 59.1 % at 6 months (CR 31.8 %, PR 27.2 %) ,The median time to response was 4 weeks (1-8 wks.) ,with 45.5 %of all patient responded within 1 month, 22.8% lost response at 1 year (accumulative 1 year response 36.3%) , further 9.1% lost response at 2 years (accumulative 2 year response 27.2 %) , 13.6% did not showed any response. Conclusion: over 2 year’s observation, our study confirms effectiveness and safety of rituximab in management of chronic refractory ITP.
机译:背景与目的:免疫性血小板减少症(ITP)的治疗始于类固醇,但大多数患者会复发或有明显的不良反应。利妥昔单抗的使用受到了热烈欢迎:它导致高达60%的缓解率,使其成为脾切除术的主要替代药物,且副作用少得多。研究目的是评估利妥昔单抗治疗慢性和难治性免疫性血小板减少性紫癜(ITP)患者2年的有效性。方法和材料:回顾性研究包括22例标记为难治性慢性特发性血小板减少性紫癜(ITP)的患者,该研究于2017年2月至2019年2月在国王侯赛因医学中心/安曼-约旦血液和肿瘤科进行,每周4剂给予利妥昔单抗375mg / m2,对利妥昔单抗的疗效和安全性进行了为期2年的定期随访。结果:诊断时的平均年龄为36.7岁(19-54岁),利妥昔单抗治疗前的平均血小板计数为8×109 / L。所有患者均随访2年,在6个月时对利妥昔单抗的总缓解率为59.1%( CR 31.8%,PR 27.2%),中位反应时间为4周(1-8周),其中45.5%的患者在1个月内缓解,1年后22.8%丧失反应(累积1年的反应为36.3%) ),则2年后仍有9.1%的患者失去反应(累积2年的患者有27.2%的反应),而13.6%则未显示任何反应。结论:经过2年的观察,我们的研究证实了利妥昔单抗在治疗慢性难治性ITP中的有效性和安全性。

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