Literature DB >> 27014570

Patient's weight can decide about spending millions on enzyme replacement therapy in MPS II.

Miroslaw Bik-Multanowski1, Ewa Jamroz2, Lukasz Kaluzny3, Ewa Pronicka4, Dariusz Rokicki4, Ewa Starostecka5, Jolanta Sykut-Cegielska6, Mieczyslaw Walczak7.   

Abstract

Entities:  

Keywords:  Enzyme replacement; Expensive therapies; MPS, mucopolysaccharidosis; Pediatric orphan disease; Public health; Walking test

Year:  2015        PMID: 27014570      PMCID: PMC4789339          DOI: 10.1016/j.ymgmr.2015.12.002

Source DB:  PubMed          Journal:  Mol Genet Metab Rep        ISSN: 2214-4269


× No keyword cloud information.
Enzyme replacement therapy in mucopolysaccharidosis type II (MPS II, Hunter disease) is extremely expensive and treatment effects are hardly predictable due to phenotypic variability [1]. We would like to address an additional problem — the paucity of robust clinical tests allowing for monitoring of effectiveness of enzymatic treatment. Since 2009 enzyme replacement therapy with idursulfase has been offered to all Polish patients with MPS II aged > 5 years, independently on disease severity. A total of 40 patients have started treatment up to date. In 26 persons treatment was eventually discontinued due to disease progression, death of the patient (two cases), or anaphylaxis (two cases). Unfortunately, reaching the consensus on treatment failure required sometimes several years of observation, as the classic clinical monitoring parameters [2], [3] were not always informative. Specifically: the distance covered in the six-minute walking test could not be applied in 20 non-ambulant patients, pulmonary function tests were performed only in older patients without intellectual disability and monitoring of liver size or of heart involvement was helpful only in those patients with significant hepatomegaly or cardiac dysfunction. Surprisingly, basic anthropometric measurements proved to be very useful for assessment of treatment effectiveness in some doubtful cases. No weight gain or even weight loss was observed in severely affected patients, contrary to those with milder disease in whom an overall anabolic effect was observed (Fig. 1). Our findings are consistent with previously published observations [4], [5] reporting decline of the linear growth in untreated children with MPS II, which started at the age of four to six years.
Fig. 1

Body weight and growth changes in studied patients with MPS II. A single female patient was marked with a dotted line. (CDC growth charts for boys; developed by the National Center for Health Statistics in collaboration with the National Center for Chronic Disease Prevention and Health Promotion, 2000).

In conclusion, we recommend thoughtful use of growth charts, as it can help to avoid wasting millions for prolonged enzymatic therapy in some cases of MPS II.

Contributors' statements

Miroslaw Bik-Multanowski analyzed data and drafted the manuscript. All authors contributed to data collection, reviewed and revised the manuscript, and approved the final manuscript as submitted.

Conflicts of interest

The authors declare no conflicts of interests.

Financial disclosure statement

The authors state that they have no financial relationships that could be relevant for the work.
  5 in total

1.  A clinical and genetic study of Hunter's syndrome. 2. Differences between the mild and severe forms.

Authors:  I D Young; P S Harper; R G Newcombe; I M Archer
Journal:  J Med Genet       Date:  1982-12       Impact factor: 6.318

2.  A phase II/III clinical study of enzyme replacement therapy with idursulfase in mucopolysaccharidosis II (Hunter syndrome).

Authors:  Joseph Muenzer; James E Wraith; Michael Beck; Roberto Giugliani; Paul Harmatz; Christine M Eng; Ashok Vellodi; Rick Martin; Uma Ramaswami; Muge Gucsavas-Calikoglu; Suresh Vijayaraghavan; Susanne Wendt; Suzanne Wendt; Ana Cristina Puga; Antonio Puga; Brian Ulbrich; Marwan Shinawi; Maureen Cleary; Diane Piper; Anne Marie Conway; Ann Marie Conway; Alan Kimura
Journal:  Genet Med       Date:  2006-08       Impact factor: 8.822

3.  Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease.

Authors:  Maurizio Scarpa; Zsuzsanna Almássy; Michael Beck; Olaf Bodamer; Iain A Bruce; Linda De Meirleir; Nathalie Guffon; Encarna Guillén-Navarro; Pauline Hensman; Simon Jones; Wolfgang Kamin; Christoph Kampmann; Christina Lampe; Christine A Lavery; Elisa Leão Teles; Bianca Link; Allan M Lund; Gunilla Malm; Susanne Pitz; Michael Rothera; Catherine Stewart; Anna Tylki-Szymańska; Ans van der Ploeg; Robert Walker; Jiri Zeman; James E Wraith
Journal:  Orphanet J Rare Dis       Date:  2011-11-07       Impact factor: 4.123

4.  Growth charts for patients with Hunter syndrome.

Authors:  Pravin Patel; Yasuyuki Suzuki; Miho Maeda; Eriko Yasuda; Tsutomu Shimada; Kenji E Orii; Tadao Orii; Shunji Tomatsu
Journal:  Mol Genet Metab Rep       Date:  2014

5.  Clinical efficacy of enzyme replacement therapy in paediatric Hunter patients, an independent study of 3.5 years.

Authors:  Rosella Tomanin; Alessandra Zanetti; Francesca D'Avanzo; Angelica Rampazzo; Nicoletta Gasparotto; Rossella Parini; Antonia Pascarella; Daniela Concolino; Elena Procopio; Agata Fiumara; Andrea Borgo; Anna Chiara Frigo; Maurizio Scarpa
Journal:  Orphanet J Rare Dis       Date:  2014-09-18       Impact factor: 4.123

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.