首页> 外文期刊>Journal of the European Academy of Dermatology and Venereology: JEADV >Antifibrotic effect after low-dose imatinib mesylate treatment in patients with nephrogenic systemic fibrosis: An open-label non-randomized, uncontrolled clinical trial
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Antifibrotic effect after low-dose imatinib mesylate treatment in patients with nephrogenic systemic fibrosis: An open-label non-randomized, uncontrolled clinical trial

机译:低剂量甲磺酸伊马替尼治疗肾原性系统性纤维化患者后的抗纤维化作用:一项开放标签的非随机,非对照临床试验

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Background Nephrogenic systemic fibrosis is a disease affecting the connective tissue of the skin and internal organs in patients with renal failure. No effective treatments are available. Objectives To investigate if the tyrosine kinase inhibitor, imatinib mesylate was effective in patients with moderate to severe nephrogenic systemic fibrosis. Methods Among 25 patients with nephrogenic systemic fibrosis evaluated for the study from 1 October 2009 to 1 December 2010, four were included. They were treated with oral imatinib mesylate at a start dose of 400 mg/day. Main outcome measure: Reduction of skin fibrosis and increase in joint mobility evaluated by the modified Rodnan skin score and a goniometer. Results In two patients, the imatinib mesylate dose was reduced to 200 mg/day and in one patient to 100 mg/day. Two patients were treated for 24 weeks, one patient for 16 weeks and one patient for 4 weeks. Three patients experienced tethering of their skin which lessened with reduction in modified Rodnan skin score from 24 to 20, 24 to 17 and 21 to 14 but with very limited changes in joint mobility. The fourth patient discontinued the treatment due to a complicating infection. Conclusion Imatinib mesylate may be an effective drug in the treatment of skin fibrosis in moderate to severe NSF cases, even at reduced doses. We found a positive clinical effect on the skin, but no convincing improvement of the joint mobility. Only few patients could be recruited limiting the interpretation and conclusions of the results.
机译:背景技术肾源性全身纤维化是一种影响肾衰竭患者皮肤和内脏器官的结缔组织的疾病。没有有效的治疗方法。目的探讨酪氨酸激酶抑制剂甲磺酸伊马替尼在中重度肾原性系统性纤维化患者中是否有效。方法从2009年10月1日至2010年12月1日对25例肾源性系统纤维化患者进行评估,包括4例。他们接受了口服甲磺酸伊马替尼的起始剂量为400毫克/天的治疗。主要结果指标:通过改良的Rodnan皮肤评分和测角仪评估皮肤纤维化的减少和关节活动度的增加。结果两名患者的甲磺酸伊马替尼剂量降低至200 mg /天,一名患者的剂量降至100 mg /天。两名患者接受了24周的治疗,一名患者接受了16周的治疗,一名患者接受了4周的治疗。三名患者的皮肤束缚减少,但改良的Rodnan皮肤评分从24降低到24、24降低到17和21降低到14,但关节活动度变化非常有限。第四名患者由于复杂的感染而中断了治疗。结论甲磺酸伊马替尼可能是中度至重度NSF患者皮肤纤维化的有效药物,即使减少剂量也是如此。我们发现对皮肤有积极的临床效果,但没有令人信服的关节活动性改善。只能招募很少的患者来限制结果的解释和结论。

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