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口服伊米苷酶(Genz-112638)治疗戈谢病 1 型:2 年 2 期研究的血液学、内脏和骨骼表现改善结果。

Improvement in hematological, visceral, and skeletal manifestations of Gaucher disease type 1 with oral eliglustat tartrate (Genz-112638) treatment: 2-year results of a phase 2 study.

机构信息

Hematology Research Center, Russian Academy of Medical Sciences, Moscow, Russia;

出版信息

Blood. 2010 Nov 18;116(20):4095-8. doi: 10.1182/blood-2010-06-293902. Epub 2010 Aug 16.

Abstract

Eliglustat tartrate is an investigational oral substrate reduction therapy for Gaucher disease type 1 that is pharmacologically distinct from intravenous enzyme replacement therapy. Eliglustat tartrate improved clinical manifestations in patients who received 50 or 100 mg twice daily for 1 year during an open-label phase 2 study (Blood. 2010;116(6):893-899). We report further improvements after 2 years of treatment in 20 patients (11 females, 9 males; mean age, 33 years) with baseline splenomegaly and thrombocytopenia and/or anemia. Statistically significant (P < .001) percentage improvements from baseline occurred in platelet count (mean ± SD, 81% ± 56%), hemoglobin level (20% ± 15%), spleen volume (-52% ± 11%), and liver volume (-24% ± 13%). Mean platelet count increased ∼ 50 000/mm(3). Mean hemoglobin level increased 2.1 g/dL overall and 3.1 g/dL in 10 patients with baseline anemia. Organ volume reductions were greatest in patients with severe baseline organomegaly. Seventeen (85%) patients met established therapeutic goals for ≥ 3 of the 4 parameters. Lumbar spine bone mineral density increased 7.8% ± 10.6% (P = .01) and T-score 0.6 ± 0.8 (P = .012), with major gains in osteoporotic and osteopenic patients. Magnetic resonance imaging assessment showed that bone marrow infiltration by Gaucher cells was decreased (8/18 patients) or stable (10/18 patients). No safety-related trends emerged during 2 years of treatment. This multisite, open-label, single-arm phase 2 study is registered at www.clinicaltrials.gov as NCT00358150.

摘要

伊米苷酶酒石酸盐是一种研究中的用于 1 型戈谢氏病的口服底物还原治疗药物,在药理学上与静脉用酶替代疗法不同。在一项开放标签的 2 期研究中,接受每日两次、每次 50 或 100mg 伊米苷酶酒石酸盐治疗 1 年的患者的临床表现得到改善(Blood. 2010;116(6):893-899)。我们报告了在 20 例基线时伴有脾肿大和血小板减少症和/或贫血的患者中,经过 2 年的治疗后进一步的改善(11 例女性,9 例男性;平均年龄 33 岁)。与基线相比,血小板计数(平均 ± 标准差,81% ± 56%)、血红蛋白水平(20% ± 15%)、脾脏体积(-52% ± 11%)和肝脏体积(-24% ± 13%)的百分比改善具有统计学意义(P <.001)。平均血小板计数增加了约 50000/mm3。总体而言,平均血红蛋白水平升高了 2.1g/dL,基线时有贫血的 10 例患者升高了 3.1g/dL。在基线时器官肿大严重的患者中,器官体积减少最大。17 例(85%)患者符合 4 项参数中≥3 项的既定治疗目标。腰椎骨密度增加 7.8% ± 10.6%(P =.01),T 评分 0.6 ± 0.8(P =.012),骨质疏松和低骨量患者的获益更大。磁共振成像评估显示戈谢氏细胞骨髓浸润减少(18 例患者中的 8 例)或稳定(18 例患者中的 10 例)。在 2 年的治疗期间未出现与安全性相关的趋势。这项多中心、开放标签、单臂 2 期研究在 www.clinicaltrials.gov 注册,编号为 NCT00358150。

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