Literature DB >> 20542712

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

Ari Zimran1, Gheona Altarescu, Deborah Elstein.   

Abstract

Because of an unpredicted and unavoidable shortage in global supplies of imiglucerase for Gaucher disease, we collected clinical and laboratory data from patients who were evaluated ≤ 6months before drug withdrawal and then retested before/during reinstatement of therapy. Hemoglobin, platelet counts, and liver and spleen index volumes by ultrasound as well as chitotriosidase were evaluated as percent change over time and relative to dose-years of exposure to enzyme therapy. Deterioration was seen in all four clinical parameters and in chitotriosidase activity in most patients and even among patients who stopped for only 3 months. No patient consistently showed nondeterioration in all five parameters. Platelet counts were most sensitive to therapy withdrawal. There was no overt correlation between percent change in these parameters and dose-years of therapy. Although we no longer think that drug vacations should be considered as a form of maintenance for patients requiring enzyme therapy for Gaucher disease, but if necessary-for compelling personal reasons-one may be reassured that a short-term drug interruption is not likely to lead to irreversible complications or return to baseline values of critical clinical parameters.
Copyright © 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20542712     DOI: 10.1016/j.bcmd.2010.05.001

Source DB:  PubMed          Journal:  Blood Cells Mol Dis        ISSN: 1079-9796            Impact factor:   3.039


  12 in total

1.  Effects of switching from a reduced dose imiglucerase to velaglucerase in type 1 Gaucher disease: clinical and biochemical outcomes.

Authors:  Laura van Dussen; Timothy M Cox; Erik J Hendriks; Elizabeth Morris; Erik M Akkerman; Mario Maas; Johanna E M Groener; Johannes M F G Aerts; Patrick B Deegan; Carla E M Hollak
Journal:  Haematologica       Date:  2012-07-06       Impact factor: 9.941

2.  Velaglucerase alfa.

Authors:  Johannes M F G Aerts; Uma Yasothan; Peter Kirkpatrick
Journal:  Nat Rev Drug Discov       Date:  2010-10-29       Impact factor: 84.694

3.  Did the temporary shortage in supply of imiglucerase have clinical consequences? Retrospective observational study on 34 italian Gaucher type I patients.

Authors:  Laura Deroma; Annalisa Sechi; Andrea Dardis; Daniela Macor; Giulia Liva; Giovanni Ciana; Bruno Bembi
Journal:  JIMD Rep       Date:  2012-07-01

4.  Value of plasma chitotriosidase to assess non-neuronopathic Gaucher disease severity and progression in the era of enzyme replacement therapy.

Authors:  L van Dussen; E J Hendriks; J E M Groener; R G Boot; C E M Hollak; J M F G Aerts
Journal:  J Inherit Metab Dis       Date:  2014-05-16       Impact factor: 4.982

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

Authors:  Timothy M Cox; Guillermo Drelichman; Renata Cravo; Manisha Balwani; Thomas Andrew Burrow; Ana Maria Martins; Elena Lukina; Barry Rosenbloom; Ozlem Goker-Alpan; Nora Watman; Amal El-Beshlawy; Priya S Kishnani; Maria Lucia Pedroso; Sebastiaan J M Gaemers; Regina Tayag; M Judith Peterschmitt
Journal:  Blood       Date:  2017-02-06       Impact factor: 22.113

Review 6.  Enzyme replacement and substrate reduction therapy for Gaucher disease.

Authors:  Elad Shemesh; Laura Deroma; Bruno Bembi; Patrick Deegan; Carla Hollak; Neal J Weinreb; Timothy M Cox
Journal:  Cochrane Database Syst Rev       Date:  2015-03-27

7.  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

8.  Consequences of a global enzyme shortage of agalsidase beta in adult Dutch Fabry patients.

Authors:  Bouwien E Smid; Saskia M Rombach; Johannes M F G Aerts; Symen Kuiper; Mina Mirzaian; Hermen S Overkleeft; Ben J H M Poorthuis; Carla E M Hollak; Johanna E M Groener; Gabor E Linthorst
Journal:  Orphanet J Rare Dis       Date:  2011-10-31       Impact factor: 4.123

9.  Impact of imiglucerase supply constraint on the therapeutic management and course of disease in French patients with Gaucher disease type 1.

Authors:  Jérôme Stirnemann; Christian Rose; Christine Serratrice; Florence Dalbies; Olivier Lidove; Agathe Masseau; Yves-Marie Pers; Camille Baron; Nadia Belmatoug
Journal:  Orphanet J Rare Dis       Date:  2015-05-13       Impact factor: 4.123

10.  Cost-effectiveness of enzyme replacement therapy for type 1 Gaucher disease.

Authors:  Laura van Dussen; Marieke Biegstraaten; Carla E M Hollak; Marcel G W Dijkgraaf
Journal:  Orphanet J Rare Dis       Date:  2014-04-14       Impact factor: 4.123

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