Giraldo Pilar, Latre Paz, Alfonso Pilar, Acedo Antonio, Alonso Dora, Barez Abelardo, Corrales Alejandro, Franco Rafael, Roldan Vanessa, Serrano Sol, Pocovi Miguel
Haematology Department, Miguel Servet University Hospital, Zaragoza, Spain.
Haematologica. 2006 May;91(5):703-6. Epub 2006 Apr 19.
In a prospective, open-label study, 25 patients with mild-to-moderate type 1 Gaucher's disease (GD1) were treated with miglustat (Zavesca), an oral glucosylceramide synthase inhibitor, over 12 months. Of the 25 patients, 10 were therapy-naïve and 15 had previously received enzyme replacement therapy (ERT). Clinical status, blood parameters, biomarkers, and organomegaly were assessed at baseline at 6 months and at 12 months. At 6 months the previously untreated patients showed a mean increase in hemoglobin of 0.77 g/dL, platelet counts improved or remaining stable, chitotriosidase and CCL18 decreased. These results were similar to those observed in 40 Spanish GD1 patients on ERT. Bone marrow infiltration cleared at 12 months. In the previously treated group, clinical and hematologic parameters and biomarkers were maintained/ improved at 12 months. Miglustat was well tolerated. The efficacy of miglustat treatment after 6 months was comparable to that of ERT.
在一项前瞻性、开放标签研究中,25例轻至中度1型戈谢病(GD1)患者接受了米格鲁司他(泽韦斯卡)治疗,这是一种口服葡糖神经酰胺合酶抑制剂,治疗时间为12个月。25例患者中,10例为初治患者,15例曾接受过酶替代疗法(ERT)。在基线、6个月和12个月时评估临床状态、血液参数、生物标志物和器官肿大情况。6个月时,之前未接受治疗的患者血红蛋白平均增加0.77g/dL,血小板计数改善或保持稳定,几丁质酶和CCL18下降。这些结果与40例接受ERT治疗的西班牙GD1患者的观察结果相似。12个月时骨髓浸润清除。在之前接受治疗的组中,临床和血液学参数以及生物标志物在12个月时维持/改善。米格鲁司他耐受性良好。6个月后米格鲁司他治疗的疗效与ERT相当。