Literature DB >> 23430505

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

Laura Deroma1, Annalisa Sechi, Andrea Dardis, Daniela Macor, Giulia Liva, Giovanni Ciana, Bruno Bembi.   

Abstract

Background. Enzyme Replacement Therapy (ERT) is the standard of care in Gaucher disease. The effects of withdrawal or reduced doses are debated, thus a retrospective cohort study was conducted to investigate clinical and laboratory differences in 34 Gaucher type 1 patients experiencing an ERT dosage reduction after the forced temporary imiglucerase shortage in 2009. Methods. Haemoglobin concentration, leukocytes and platelets counts, and chitotriosidase activity were assessed at baseline and after 6 and 12 months (t0, t6, t12), while bone pain, energy, work or school performance, concentration, memory and social life every 3 months. Results. The cohort was made up of 18 males and 16 females (medians: age 41.8 years, therapy duration 14.1 years, dosage reduction 35.5%). Haemoglobin, leukocytes and platelets remained substantially stable, while chitotriosidase activity showed an increase, especially after t6. Age, splenectomy or genotype were not associated with laboratory parameters changes, except for a significant median increase of chitotriosidase activity in non-splenectomised patients after 12 months (p = 0.01). At 3, 6, 9 and 12 months, more than 50% patients reported at least one problem in subjective well-being (56%, 65%, 70%, 58%, respectively), while bone pain occurred or worsened in 13/33, 13/32, 7/28 and 5/26 patients, respectively. No bone crises were reported. Conclusions. Drug reduction did not induce substantial modification in the laboratory values but seems to have influenced the well-being perception of some Gaucher patients. Thus, bone pain, general health and quality of life should be carefully monitored during ERT reductions.

Entities:  

Year:  2012        PMID: 23430505      PMCID: PMC3575042          DOI: 10.1007/8904_2012_158

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  14 in total

1.  Changes in serum chitotriosidase activity with cessation of replacement enzyme (cerebrosidase) administration in Gaucher disease.

Authors:  B Czartoryska; A Tylki-Szymańska; A Lugowska
Journal:  Clin Biochem       Date:  2000-03       Impact factor: 3.281

2.  Clinical monitoring after cessation of enzyme replacement therapy in M. Gaucher.

Authors:  S vom Dahl; L W Poll; D Häussinger
Journal:  Br J Haematol       Date:  2001-06       Impact factor: 6.998

3.  Effects of imilglucerase withdrawal on an adult with Gaucher disease.

Authors:  I V Schwartz; S Karam; P Ashton-Prolla; K Michelin; J Coelho; R F Pires; M L Pereira; R Giugliani
Journal:  Br J Haematol       Date:  2001-06       Impact factor: 6.998

Review 4.  Gaucher disease: pathological mechanisms and modern management.

Authors:  Marina Jmoudiak; Anthony H Futerman
Journal:  Br J Haematol       Date:  2005-04       Impact factor: 6.998

Review 5.  The pathophysiology of GD - current understanding and rationale for existing and emerging therapeutic approaches.

Authors:  Derralynn A Hughes; Gregory M Pastores
Journal:  Wien Med Wochenschr       Date:  2010-12

6.  Withdrawal of enzyme replacement therapy in Gaucher's disease.

Authors:  D Elstein; A Abrahamov; I Hadas-Halpern; A Zimran
Journal:  Br J Haematol       Date:  2000-08       Impact factor: 6.998

Review 7.  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

8.  Clinical consequences of interrupting enzyme replacement therapy in children with type 1 Gaucher disease.

Authors:  Guillermo Drelichman; Elvira Ponce; Nora Basack; Daniel Freigeiro; Luis Aversa; Elena Graciela; Regina Kohan
Journal:  J Pediatr       Date:  2007-06-22       Impact factor: 4.406

9.  Force majeure: therapeutic measures in response to restricted supply of imiglucerase (Cerezyme) for patients with Gaucher disease.

Authors:  Carla E M Hollak; Stephan vom Dahl; Johannes M F G Aerts; Nadia Belmatoug; Bruno Bembi; Yossi Cohen; Tanya Collin-Histed; Patrick Deegan; Laura van Dussen; Pilar Giraldo; Eugen Mengel; Helen Michelakakis; Jeremy Manuel; Martin Hrebicek; Rosella Parini; Jörg Reinke; Maja di Rocco; Miguel Pocovi; Maria Clara Sa Miranda; Anna Tylki-Szymanska; Ari Zimran; Timothy M Cox
Journal:  Blood Cells Mol Dis       Date:  2009-10-04       Impact factor: 3.039

10.  Cessation of enzyme replacement therapy in Gaucher disease.

Authors:  Karen A Grinzaid; Eleanor Geller; Soheil L Hanna; Louis J Elsas
Journal:  Genet Med       Date:  2002 Nov-Dec       Impact factor: 8.822

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  8 in total

1.  Intra-monocyte Pharmacokinetics of Imiglucerase Supports a Possible Personalized Management of Gaucher Disease Type 1.

Authors:  Juliette Berger; Marie Vigan; Bruno Pereira; Thu Thuy Nguyen; Roseline Froissart; Nadia Belmatoug; Florence Dalbiès; Agathe Masseau; Christian Rose; Christine Serratrice; Yves-Marie Pers; Ivan Bertchansky; Fabrice Camou; Monia Bengherbia; Céline Bourgne; Catherine Caillaud; Magali Pettazzoni; Amina Berrahal; Jérôme Stirnemann; France Mentré; Marc G Berger
Journal:  Clin Pharmacokinet       Date:  2019-04       Impact factor: 6.447

Review 2.  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

3.  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

Review 4.  Imiglucerase in the management of Gaucher disease type 1: an evidence-based review of its place in therapy.

Authors:  Christine Serratrice; Sebastian Carballo; Jacques Serratrice; Jérome Stirnemann
Journal:  Core Evid       Date:  2016-10-14

5.  The European Gaucher Alliance: a survey of member patient organisations' activities, healthcare environments and concerns.

Authors:  Irena Žnidar; Tanya Collin-Histed; Pascal Niemeyer; Johanna Parkkinen; Anne-Grethe Lauridsen; Sandra Zariņa; Yossi Cohen; Jeremy Manuel
Journal:  Orphanet J Rare Dis       Date:  2014-09-02       Impact factor: 4.123

6.  Gaucher disease in a family from Maranhão.

Authors:  Samira Shizuko Parreão Oi; Dario Itapary Nicolau; Sebastião Kelson Alves Dos Santos; Marcos Antonio Custódio Neto da Silva; Graça Maria de Castro Viana; Maria do Desterro Soares Brandão Nascimento
Journal:  Rev Bras Hematol Hemoter       Date:  2014-07-19

7.  Impact of imiglucerase supply shortage on clinical and laboratory parameters in Norrbottnian patients with Gaucher disease type 3.

Authors:  Maciej Machaczka; Cecilia Kämpe Björkvall; Joanna Wieremiejczyk; Martin Paucar Arce; Kristina Myhr-Eriksson; Monika Klimkowska; Hans Hägglund; Per Svenningsson
Journal:  Arch Immunol Ther Exp (Warsz)       Date:  2014-09-10       Impact factor: 4.291

8.  Health-related quality of life in children and adolescents living with Gaucher disease and their parents.

Authors:  Eduardo Remor; Antonio Baldellou
Journal:  Health Psychol Behav Med       Date:  2018-04-12
  8 in total

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