Literature DB >> 28167660

Eliglustat maintains long-term clinical stability in patients with Gaucher disease type 1 stabilized on enzyme therapy.

Timothy M Cox1, Guillermo Drelichman2, Renata Cravo3, Manisha Balwani4, Thomas Andrew Burrow5, Ana Maria Martins6, Elena Lukina7, Barry Rosenbloom8, Ozlem Goker-Alpan9, Nora Watman10, Amal El-Beshlawy11, Priya S Kishnani12, Maria Lucia Pedroso13, Sebastiaan J M Gaemers14, Regina Tayag15, M Judith Peterschmitt14.   

Abstract

In the phase 3 Study of Eliglustat Tartrate (Genz-112638) in Patients With Gaucher Disease Who Have Reached Therapeutic Goals With Enzyme Replacement Therapy (ENCORE), at 1 year, eliglustat was noninferior to imiglucerase enzyme therapy in maintaining stable platelet counts, hemoglobin concentrations, and spleen and liver volumes. After this primary analysis period, patients entered a long-term extension phase in which all received eliglustat. Duration on eliglustat ranged from 2 to 5 years, depending on timing of enrollment (which spanned 2 years), treatment group to which patients were randomized, and whether they lived in the United States when commercial eliglustat became available. Here we report long-term safety and efficacy of eliglustat for 157 patients who received eliglustat in the ENCORE trial; data are available for 46 patients who received eliglustat for 4 years. Mean hemoglobin concentration, platelet count, and spleen and liver volumes remained stable for up to 4 years. Year to year, all 4 measures remained collectively stable (composite end point relative to baseline values) in ≥85% of patients as well as individually in ≥92%. Mean bone mineral density z scores (lumbar spine and femur) remained stable and were maintained in the healthy reference range throughout. Eliglustat was well tolerated over 4 years; 4 (2.5%) patients withdrew because of adverse events that were considered related to the study drug. No new or long-term safety concerns were identified. Clinical stability assessed by composite and individual measures was maintained in adults with Gaucher disease type 1 treated with eliglustat who remained in the ENCORE trial for up to 4 years. This trial was registered at www.clinicaltrials.gov as #NCT00943111.
© 2017 by The American Society of Hematology.

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Year:  2017        PMID: 28167660      PMCID: PMC5409450          DOI: 10.1182/blood-2016-12-758409

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  24 in total

1.  Phenotype, diagnosis, and treatment of Gaucher's disease.

Authors:  Gregory A Grabowski
Journal:  Lancet       Date:  2008-10-04       Impact factor: 79.321

2.  Gaucher disease and cancer incidence: a study from the Gaucher Registry.

Authors:  Barry E Rosenbloom; Neal J Weinreb; Ari Zimran; Katherine A Kacena; Joel Charrow; Elizabeth Ward
Journal:  Blood       Date:  2005-02-17       Impact factor: 22.113

3.  Effect of oral eliglustat on splenomegaly in patients with Gaucher disease type 1: the ENGAGE randomized clinical trial.

Authors:  Pramod K Mistry; Elena Lukina; Hadhami Ben Turkia; Dominick Amato; Hagit Baris; Majed Dasouki; Marwan Ghosn; Atul Mehta; Seymour Packman; Gregory Pastores; Milan Petakov; Sarit Assouline; Manisha Balwani; Sumita Danda; Evgueniy Hadjiev; Andres Ortega; Suma Shankar; Maria Helena Solano; Leorah Ross; Jennifer Angell; M Judith Peterschmitt
Journal:  JAMA       Date:  2015-02-17       Impact factor: 56.272

4.  Nonprecipitous changes upon withdrawal from imiglucerase for Gaucher disease because of a shortage in supply.

Authors:  Ari Zimran; Gheona Altarescu; Deborah Elstein
Journal:  Blood Cells Mol Dis       Date:  2010-06-09       Impact factor: 3.039

5.  A pooled analysis of adverse events in 393 adults with Gaucher disease type 1 from four clinical trials of oral eliglustat: Evaluation of frequency, timing, and duration.

Authors:  M Judith Peterschmitt; Gerald F Cox; Jennifer Ibrahim; James MacDougall; Lisa H Underhill; Palni Patel; Sebastiaan J M Gaemers
Journal:  Blood Cells Mol Dis       Date:  2017-01-13       Impact factor: 3.039

6.  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.

Authors:  Elena Lukina; Nora Watman; Elsa Avila Arreguin; Marta Dragosky; Marcelo Iastrebner; Hanna Rosenbaum; Mici Phillips; Gregory M Pastores; Ravi S Kamath; Daniel I Rosenthal; Mathilde Kaper; Tejdip Singh; Ana Cristina Puga; M Judith Peterschmitt
Journal:  Blood       Date:  2010-08-16       Impact factor: 22.113

Review 7.  Management and monitoring recommendations for the use of eliglustat in adults with type 1 Gaucher disease in Europe.

Authors:  Nadia Belmatoug; Maja Di Rocco; Cristina Fraga; Pilar Giraldo; Derralynn Hughes; Elena Lukina; Pierre Maison-Blanche; Martin Merkel; Claus Niederau; Ursula Plӧckinger; Johan Richter; Thomas M Stulnig; Stephan Vom Dahl; Timothy M Cox
Journal:  Eur J Intern Med       Date:  2016-08-10       Impact factor: 4.487

Review 8.  Therapeutic goals in the treatment of Gaucher disease.

Authors:  Gregory M Pastores; Neal J Weinreb; Hans Aerts; Generoso Andria; Timothy M Cox; Manuel Giralt; Gregory A Grabowski; Pramod K Mistry; Anna Tylki-Szymańska
Journal:  Semin Hematol       Date:  2004-10       Impact factor: 3.851

9.  Evaluation of miglustat as maintenance therapy after enzyme therapy in adults with stable type 1 Gaucher disease: a prospective, open-label non-inferiority study.

Authors:  Timothy M Cox; Dominick Amato; Carla Em Hollak; Cecile Luzy; Mariabeth Silkey; Ruben Giorgino; Robert D Steiner
Journal:  Orphanet J Rare Dis       Date:  2012-12-27       Impact factor: 4.123

10.  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
Journal:  Skeletal Radiol       Date:  2014-05-10       Impact factor: 2.199

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1.  Response to Letter to the Editor on "Enzyme Replacement or Substrate Reduction? A Review of Gaucher Disease Treatment Options".

Authors:  Alison Van Rossum; Megan Holsopple
Journal:  Hosp Pharm       Date:  2017-11-09

2.  Letter to the Editor on "Enzyme Replacement or Substrate Reduction? A Review of Gaucher Disease Treatment Options".

Authors:  Jennifer Ibrahim; Rebecca Call
Journal:  Hosp Pharm       Date:  2017-10-10

3.  Long-term eliglustat treatment of Gaucher patients over up to 10 years in Vienna.

Authors:  Thomas M Stulnig
Journal:  Wien Klin Wochenschr       Date:  2022-04-12       Impact factor: 1.704

4.  Incremental biomarker and clinical outcomes after switch from enzyme therapy to eliglustat substrate reduction therapy in Gaucher disease.

Authors:  Nathaniel Kleytman; Jiapeng Ruan; Audrey Ruan; Bailin Zhang; Vagishwari Murugesan; Haiqun Lin; Lilu Guo; Katherine Klinger; Pramod K Mistry
Journal:  Mol Genet Metab Rep       Date:  2021-08-28

5.  Role of β-glucosidase 2 in aberrant glycosphingolipid metabolism: model of glucocerebrosidase deficiency in zebrafish.

Authors:  Lindsey T Lelieveld; Mina Mirzaian; Chi-Lin Kuo; Marta Artola; Maria J Ferraz; Remco E A Peter; Hisako Akiyama; Peter Greimel; Richard J B H N van den Berg; Herman S Overkleeft; Rolf G Boot; Annemarie H Meijer; Johannes M F G Aerts
Journal:  J Lipid Res       Date:  2019-09-27       Impact factor: 5.922

6.  Tandem mass spectrometry assay of β-glucocerebrosidase activity in dried blood spots eliminates false positives detected in fluorescence assay.

Authors:  Pavlina Wolf; Roy N Alcalay; Christopher Liong; Emmaline Cullen; Michael W Pauciulo; William C Nichols; Ziv Gan-Or; Wendy K Chung; Tina Faulkner; Christopher Bentis; Robert J Pomponio; Xiwen Ma; X Kate Zhang; Joan M Keutzer; Petra Oliva
Journal:  Mol Genet Metab       Date:  2017-10-23       Impact factor: 4.797

7.  Pharmacotherapy of Gaucher Disease: Current and Future Options.

Authors:  Lunawati L Bennett; Chris Fellner
Journal:  P T       Date:  2018-05

8.  Substrate Reduction Therapy for Sandhoff Disease through Inhibition of Glucosylceramide Synthase Activity.

Authors:  John Marshall; Jennifer B Nietupski; Hyejung Park; James Cao; Dinesh S Bangari; Cristina Silvescu; Terry Wilper; Kristen Randall; Drew Tietz; Bing Wang; Xiaoyou Ying; John P Leonard; Seng H Cheng
Journal:  Mol Ther       Date:  2019-06-04       Impact factor: 11.454

9.  Case report of unexpected gastrointestinal involvement in type 1 Gaucher disease: comparison of eliglustat tartrate treatment and enzyme replacement therapy.

Authors:  Yoo-Mi Kim; Dong Hoon Shin; Su Bum Park; Chong Kun Cheon; Han-Wook Yoo
Journal:  BMC Med Genet       Date:  2017-05-15       Impact factor: 2.103

10.  Treatment of profound thrombocytopenia in a patient with Gaucher disease type 1: Is there a role for substrate reduction therapy.

Authors:  Christine I Ha; Stephanie DeArmey; Heidi Cope; Mugdha Rairikar; Priya S Kishnani
Journal:  Mol Genet Metab Rep       Date:  2017-06-22
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