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Alternative laronidase dose regimen for patients with mucopolysaccharidosis I: a multinational, retrospective, chart review case series.
Horovitz, Dafne Dain Gandelman; Acosta, Angelina X; Giugliani, Roberto; Hlavatá, Anna; Hlavatá, Katarína; Tchan, Michel C; Lopes Barth, Anneliese; Cardoso, Laercio; Embiruçu de Araújo Leão, Emília Katiane; Esposito, Ana Carolina; Kyosen, Sandra Obikawa; De Souza, Carolina Fischinger Moura; Martins, Ana Maria.
Afiliación
  • Horovitz DD; Instituto Nacional de Saude da Mulher, da Criança e do Adolescente Fernandes Figueira - Fiocruz, Rio de Janeiro, Brazil. dafne@iff.fiocruz.br.
  • Acosta AX; Departamento de Pediatria, Serviço de Genética Médica, Universidade Federal da Bahia, Salvador, BA, Brazil.
  • Giugliani R; Medical Genetics Service, Hospital de Clinicas de Alegre, Porto Alegre, Brazil.
  • Hlavatá A; 2nd Department of Pediatrics, Comenius University Children´s Hospital, Bratislava, Slovakia.
  • Hlavatá K; 2nd Department of Pediatrics, Comenius University Children´s Hospital, Bratislava, Slovakia.
  • Tchan MC; Department of Genetic Medicine, Westmead Hospital and Sydney University, Sydney, Australia.
  • Lopes Barth A; Instituto Nacional de Saude da Mulher, da Criança e do Adolescente Fernandes Figueira - Fiocruz, Rio de Janeiro, Brazil.
  • Cardoso L; Departamento de Pediatria, Serviço de Genética Médica, Universidade Federal da Bahia, Salvador, BA, Brazil.
  • Embiruçu de Araújo Leão EK; Departamento de Pediatria, Serviço de Genética Médica, Universidade Federal da Bahia, Salvador, BA, Brazil.
  • Esposito AC; Instituto Nacional de Saude da Mulher, da Criança e do Adolescente Fernandes Figueira - Fiocruz, Rio de Janeiro, Brazil.
  • Kyosen SO; Department of Pediatrics, Universidade Federal de Sao Paulo, São Paulo, Brazil.
  • De Souza CF; Medical Genetics Service, Hospital de Clinicas de Alegre, Porto Alegre, Brazil.
  • Martins AM; Department of Pediatrics, Universidade Federal de Sao Paulo, São Paulo, Brazil.
Orphanet J Rare Dis ; 11(1): 51, 2016 04 29.
Article en En | MEDLINE | ID: mdl-27129473
ABSTRACT

BACKGROUND:

Enzyme replacement therapy (ERT) with laronidase (recombinant human α-L-iduronidase, Aldurazyme®) is indicated for non-neurological signs and symptoms of mucopolysaccharidosis type I (MPS I). The approved laronidase dose regimen is weekly infusions of 0.58mg/kg, however, patients and caregivers may have difficulty complying with the weekly regimen. We examined clinical outcomes, tolerability, compliance, and satisfaction in a series of patients who switched to every other week infusions.

METHODS:

This multinational, retrospective, chart review case series analyzed data from 20 patients who had undergone ERT with laronidase 0.58mg/kg weekly for more than one year, and who then switched to 1.2mg/kg every other week.

RESULTS:

The majority of patients had attenuated MPS I phenotypes (9 with Hurler-Scheie and 8 with Scheie syndromes) and 3 patients had severe MPS I (Hurler syndrome). Most patients presented with organomegaly (17/20), umbilical and/or inguinal hernia (16/20), cardiac abnormalities (17/20), musculoskeletal abnormalities (19/20), and neurological and/or developmental deficits (15/20). Following laronidase treatment, signs stabilized or improved. No deterioration or reversal of clinical outcome was noted in any patient who switched from the weekly dose of 0.58mg.kg to 1.2mg/kg every other week. There were no safety issues during the duration of every other week dosing. Patient compliance and satisfaction with the dosing regimen were greater with every other week dosing than weekly dosing.

CONCLUSIONS:

An alternative dose regimen of 1.2mg/kg laronidase every other week was well tolerated and clinically similar to the standard dose for patients who were stabilized with weekly 0.58 mg/kg for one year or more. When an individualized approach to laronidase therapy is necessary, every other week dosing may be an alternative for patients with difficulty receiving weekly infusions.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Mucopolisacaridosis I / Iduronidasa Tipo de estudio: Observational_studies Límite: Adolescent / Adult / Child / Child, preschool / Humans / Infant Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2016 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Mucopolisacaridosis I / Iduronidasa Tipo de estudio: Observational_studies Límite: Adolescent / Adult / Child / Child, preschool / Humans / Infant Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2016 Tipo del documento: Article País de afiliación: Brasil