Literature DB >> 25822821

The Kuvan(®) Adult Maternal Paediatric European Registry (KAMPER) Multinational Observational Study: Baseline and 1-Year Data in Phenylketonuria Patients Responsive to Sapropterin.

Friedrich K Trefz1, Ania C Muntau, Florian B Lagler, Flavie Moreau, Jan Alm, Alberto Burlina, Frank Rutsch, Amaya Bélanger-Quintana, François Feillet.   

Abstract

INTRODUCTION: Sapropterin dihydrochloride (Kuvan(®)), a synthetic 6R-diastereoisomer of tetrahydrobiopterin (BH4), is approved in Europe for the treatment of patients aged ≥4 years with hyperphenylalaninaemia (HPA) due to BH4-responsive phenylalanine hydroxylase (PAH) deficiency, in conjunction with a phenylalanine-restricted diet, and also for the treatment of patients with BH4 deficiency. AIMS/
METHODS: KAMPER is an ongoing, observational, multicentre registry with the primary objective of providing information over 15 years on long-term safety of sapropterin dihydrochloride treatment in patients with HPA. Here we report initial data on characteristics from patients recruited by the time of the third interim analysis and results at 1 year.
RESULTS: Overall, 325 patients from 55 sites in seven European countries were included in the analysis: 296 (91.1%) patients with PAH deficiency (median [Q1, Q3] age, 10.3 [7.2, 15.0] years) and 29 (8.9%) with BH4 deficiency (12.8 [6.6, 18.9] years). Fifty-nine patients (18.2%) were aged ≥18 years; 4 patients were pregnant. No elderly patients (aged ≥65 years) or patients with renal or hepatic insufficiency were enroled in the study. Twelve-month data were available for 164 patients with PAH deficiency and 16 with BH4 deficiency. No new safety concerns were identified as of May 2013.
CONCLUSIONS: Initial data from KAMPER show that sapropterin dihydrochloride has a favourable safety profile. Registry data collected over time will provide insight into the management and outcomes of patients with PAH deficiency and BH4 deficiency, including long-term safety, impact on growth and neurocognitive outcomes and the effect of sapropterin dihydrochloride treatment on populations of special interest.

Entities:  

Year:  2015        PMID: 25822821      PMCID: PMC4484899          DOI: 10.1007/8904_2015_425

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


  19 in total

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Journal:  Lancet       Date:  2010-10-23       Impact factor: 79.321

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Authors:  N Blau; I Barnes; J L Dhondt
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

4.  Partial purification and characterization of tryptophan hydroxylase from rabbit hindbrain.

Authors:  P A Friedman; A H Kappelman; S Kaufman
Journal:  J Biol Chem       Date:  1972-07-10       Impact factor: 5.157

5.  Use of sapropterin dihydrochloride in maternal phenylketonuria. A European experience of eight cases.

Authors:  François Feillet; Ania C Muntau; François-Guillaume Debray; Amelie S Lotz-Havla; Alexandra Puchwein-Schwepcke; Ma'atem Béatrice Fofou-Caillierez; Francjan van Spronsen; Fritz Friedrich Trefz
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7.  Long-term treatment and diagnosis of tetrahydrobiopterin-responsive hyperphenylalaninemia with a mutant phenylalanine hydroxylase gene.

Authors:  Haruo Shintaku; Shigeo Kure; Toshihiro Ohura; Yoshiyuki Okano; Misao Ohwada; Naruji Sugiyama; Nobuo Sakura; Ichiro Yoshida; Makoto Yoshino; Yoichi Matsubara; Ken Suzuki; Kikumaro Aoki; Teruo Kitagawa
Journal:  Pediatr Res       Date:  2003-12-17       Impact factor: 3.756

8.  Assessment of tetrahydrobiopterin (BH4) responsiveness in phenylketonuria.

Authors:  Betina Fiege; Nenad Blau
Journal:  J Pediatr       Date:  2007-06       Impact factor: 4.406

9.  Long-term follow-up and outcome of phenylketonuria patients on sapropterin: a retrospective study.

Authors:  Stefanie Keil; Karen Anjema; Francjan J van Spronsen; Nilo Lambruschini; Alberto Burlina; Amaya Bélanger-Quintana; Maria L Couce; Francois Feillet; Roberto Cerone; Amelie S Lotz-Havla; Ania C Muntau; Annet M Bosch; Concetta A P Meli; Thierry Billette de Villemeur; Ilse Kern; Enrica Riva; Marcello Giovannini; Lena Damaj; Vincenzo Leuzzi; Nenad Blau
Journal:  Pediatrics       Date:  2013-05-20       Impact factor: 7.124

10.  The response of patients with phenylketonuria and elevated serum phenylalanine to treatment with oral sapropterin dihydrochloride (6R-tetrahydrobiopterin): a phase II, multicentre, open-label, screening study.

Authors:  B K Burton; D K Grange; A Milanowski; G Vockley; F Feillet; E A Crombez; V Abadie; C O Harding; S Cederbaum; D Dobbelaere; A Smith; A Dorenbaum
Journal:  J Inherit Metab Dis       Date:  2007-09-12       Impact factor: 4.982

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  5 in total

Review 1.  Tetrahydrobipterin-responsive phenylalanine hydroxylase deficiency.

Authors:  Shigeo Kure; Haruo Shintaku
Journal:  J Hum Genet       Date:  2018-11-30       Impact factor: 3.172

Review 2.  The complete European guidelines on phenylketonuria: diagnosis and treatment.

Authors:  A M J van Wegberg; A MacDonald; K Ahring; A Bélanger-Quintana; N Blau; A M Bosch; A Burlina; J Campistol; F Feillet; M Giżewska; S C Huijbregts; S Kearney; V Leuzzi; F Maillot; A C Muntau; M van Rijn; F Trefz; J H Walter; F J van Spronsen
Journal:  Orphanet J Rare Dis       Date:  2017-10-12       Impact factor: 4.123

Review 3.  The Utility of Genomic Testing for Hyperphenylalaninemia.

Authors:  Elisabetta Anna Tendi; Maria Guarnaccia; Giovanna Morello; Sebastiano Cavallaro
Journal:  J Clin Med       Date:  2022-02-18       Impact factor: 4.964

4.  One-year follow-up of B vitamin and Iron status in patients with phenylketonuria provided tetrahydrobiopterin (BH4).

Authors:  Kristen D Brantley; Teresa D Douglas; Rani H Singh
Journal:  Orphanet J Rare Dis       Date:  2018-10-30       Impact factor: 4.123

Review 5.  Similarities and differences in key diagnosis, treatment, and management approaches for PAH deficiency in the United States and Europe.

Authors:  Tracy Brock Lowe; Jane DeLuca; Georgianne L Arnold
Journal:  Orphanet J Rare Dis       Date:  2020-09-25       Impact factor: 4.123

  5 in total

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