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Published in: Skeletal Radiology 10/2014

Open Access 01-10-2014 | Scientific Article

Skeletal improvement in patients with Gaucher disease type 1: a phase 2 trial of oral eliglustat

Authors: Ravi S. Kamath, Elena Lukina, Nora Watman, Marta Dragosky, Gregory M. Pastores, Elsa Avila Arreguin, Hanna Rosenbaum, Ari Zimran, Rasha Aguzzi, Ana Cristina Puga, Andrea M. Norfleet, M. Judith Peterschmitt, Daniel I. Rosenthal

Published in: Skeletal Radiology | Issue 10/2014

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Abstract

Objective

Eliglustat is an investigational oral substrate reduction therapy for Gaucher disease type 1 (GD1). Its skeletal effects were evaluated by prospective monitoring of bone mineral density (BMD), fractures, marrow infiltration by Gaucher cells, focal bone lesions, and infarcts during an open-label, multi-site, single-arm phase 2 trial (NCT00358150).

Materials and methods

Institutional review board approval and patient informed consent were obtained. Eliglustat (50 or 100 mg) was self-administered by mouth twice daily; 19 patients completed 4 years of treatment. All were skeletally mature (age range, 18–55 years). DXA and MRI assessments were conducted at baseline and annually thereafter. X-rays were obtained annually until month 24, and then every other year.

Results

Lumbar spine BMD increased significantly (p = 0.02; n = 15) by a mean (SD) of 9.9 % (14.2 %) from baseline to year 4; corresponding T-scores increased significantly (p = 0.01) from a mean (SD) of −1.6 (1.1) to −0.9 (1.3). Mean femur T-score remained normal through 4 years. Femur MRI showed that 10/18 (56 %) patients had decreased Gaucher cell infiltration compared to baseline; one patient with early improvement had transient worsening at year 4. There were no lumbar spine or femoral fractures and no reported bone crises during the study. At baseline, 8/19 (42 %) patients had focal bone lesions, which remained stable, and 7/19 (37 %) patients had bone infarctions, which improved in one patient by year 2. At year 4, one new asymptomatic, indeterminate bone lesion was discovered that subsequently resolved.

Conclusions

Eliglustat may be a therapeutic option for treating the skeletal manifestations of GD1.
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Metadata
Title
Skeletal improvement in patients with Gaucher disease type 1: a phase 2 trial of oral eliglustat
Authors
Ravi S. Kamath
Elena Lukina
Nora Watman
Marta Dragosky
Gregory M. Pastores
Elsa Avila Arreguin
Hanna Rosenbaum
Ari Zimran
Rasha Aguzzi
Ana Cristina Puga
Andrea M. Norfleet
M. Judith Peterschmitt
Daniel I. Rosenthal
Publication date
01-10-2014
Publisher
Springer Berlin Heidelberg
Published in
Skeletal Radiology / Issue 10/2014
Print ISSN: 0364-2348
Electronic ISSN: 1432-2161
DOI
https://doi.org/10.1007/s00256-014-1891-9

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