首页> 美国卫生研究院文献>Molecular Genetics and Metabolism Reports >Clinical response to eliglustat in treatment-naïve patients with Gaucher disease type 1: Post-hoc comparison to imiglucerase-treated patients enrolled in the International Collaborative Gaucher Group Gaucher Registry
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Clinical response to eliglustat in treatment-naïve patients with Gaucher disease type 1: Post-hoc comparison to imiglucerase-treated patients enrolled in the International Collaborative Gaucher Group Gaucher Registry

机译:国际合作Gaucher集团Gaucher注册中心的未接受过Gaucher疾病类型1的初治患者对依格鲁司特的临床反应:事后比较与伊米苷酶治疗的患者

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摘要

Eliglustat is a recently approved oral therapy in the United States and Europe for adults with Gaucher disease type 1 who are CYP2D6 extensive, intermediate, or poor metabolizers (> 90% of patients) that has been shown to decrease spleen and liver volume and increase hemoglobin concentrations and platelet counts in untreated adults with Gaucher disease type 1 and maintain these parameters in patients previously stabilized on enzyme replacement therapy. In a post-hoc analysis, we compared the results of eliglustat treatment in treatment-naïve patients in two clinical studies with the results of imiglucerase treatment among a cohort of treatment-naïve patients with comparable baseline hematologic and visceral parameters in the International Collaborative Gaucher Group Gaucher Registry. Organ volumes and hematologic parameters improved from baseline in both treatment groups, with a time course and degree of improvement in eliglustat-treated patients similar to imiglucerase-treated patients.
机译:Eliglustat是美国和欧洲最近批准的针对Gaucher疾病1型,CYP2D6广泛,中度或弱代谢者(> 90%的患者)的成年人的口服疗法,已显示可减少脾脏和肝脏体积并增加血红蛋白未经治疗的成人高雪氏病1型患者的血药浓度和血小板计数,并在先前通过酶替代疗法稳定的患者中维持这些参数。在事后分析中,我们比较了国际合作Gaucher组中两组具有相同基线血液学和内脏参数的未治疗患者中两项临床研究中未接受过依格司他治疗的结果与伊米苷酶治疗的结果高歇注册表。在两个治疗组中,器官体积和血液学参数均较基线水平有所改善,与依格苷酶治疗的患者相似,依格司他治疗的患者随时间推移和改善程度有所提高。

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