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本文引用的文献

1
Safety, tolerability, and pharmacokinetics of eliglustat tartrate (Genz-112638) after single doses, multiple doses, and food in healthy volunteers.在健康志愿者中单次、多次和进食后给予伊格司他丁酒石酸盐(Genz-112638)的安全性、耐受性和药代动力学。
J Clin Pharmacol. 2011 May;51(5):695-705. doi: 10.1177/0091270010372387. Epub 2010 Sep 23.
2
The neurological manifestations of Gaucher disease type 1: the French Observatoire on Gaucher disease (FROG).戈谢氏病 1 型的神经表现:法国戈谢氏病观察站(FROG)。
J Inherit Metab Dis. 2010 Aug;33(4):331-8. doi: 10.1007/s10545-010-9095-5. Epub 2010 Jun 2.
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A phase 2 study of eliglustat tartrate (Genz-112638), an oral substrate reduction therapy for Gaucher disease type 1.一项关于伊曲康唑(Genz-112638)的 2 期研究,这是一种用于治疗 1 型戈谢病的口服底物减少疗法。
Blood. 2010 Aug 12;116(6):893-9. doi: 10.1182/blood-2010-03-273151. Epub 2010 May 3.
4
Official Positions of the International Society for Clinical Densitometry and executive summary of the 2007 ISCD Position Development Conference.国际临床骨密度测量学会官方立场及2007年国际临床骨密度测量学会立场发展会议执行摘要。
J Clin Densitom. 2008 Jan-Mar;11(1):75-91. doi: 10.1016/j.jocd.2007.12.007.
5
A specific and potent inhibitor of glucosylceramide synthase for substrate inhibition therapy of Gaucher disease.一种用于戈谢病底物抑制疗法的特异性强效葡糖神经酰胺合酶抑制剂。
Mol Genet Metab. 2007 Jul;91(3):259-67. doi: 10.1016/j.ymgme.2007.04.001. Epub 2007 May 16.
6
Evidence-based recommendations for monitoring bone disease and the response to enzyme replacement therapy in Gaucher patients.戈谢病患者骨病监测及酶替代疗法反应的循证医学建议
Curr Med Res Opin. 2006 Jun;22(6):1045-64. doi: 10.1185/030079906X104623.
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Gaucher disease type 1: revised recommendations on evaluations and monitoring for adult patients.1型戈谢病:成人患者评估与监测的修订建议
Semin Hematol. 2004 Oct;41(4 Suppl 5):15-22. doi: 10.1053/j.seminhematol.2004.07.010.
8
Therapeutic goals in the treatment of Gaucher disease.戈谢病治疗的治疗目标。
Semin Hematol. 2004 Oct;41(4 Suppl 5):4-14. doi: 10.1053/j.seminhematol.2004.07.009.
9
Gaucher disease: alendronate disodium improves bone mineral density in adults receiving enzyme therapy.
Blood. 2004 Sep 1;104(5):1253-7. doi: 10.1182/blood-2003-11-3854. Epub 2004 Mar 9.
10
Enzyme therapy in type 1 Gaucher disease: comparative efficacy of mannose-terminated glucocerebrosidase from natural and recombinant sources.1型戈谢病的酶替代疗法:天然来源和重组来源的甘露糖末端葡萄糖脑苷脂酶的疗效比较
Ann Intern Med. 1995 Jan 1;122(1):33-9. doi: 10.7326/0003-4819-122-1-199501010-00005.

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.

DOI:10.1182/blood-2010-06-293902
PMID:20713962
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2993616/
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。