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Efficacy and safety of intravenous laronidase for mucopolysaccharidosis type I: A systematic review and meta-analysis.
Dornelles, Alícia Dorneles; Artigalás, Osvaldo; da Silva, André Anjos; Ardila, Dora Lucia Vallejo; Alegra, Taciane; Pereira, Tiago Veiga; Vairo, Filippo Pinto E; Schwartz, Ida Vanessa Doederlein.
Afiliação
  • Dornelles AD; Postgraduate Program in Genetics Applied to Medicine, Department of Pediatrics, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
  • Artigalás O; Hospital Materno-Infantil Presidente Vargas, Porto Alegre, RS, Brazil.
  • da Silva AA; Clinical Genetics Unit, Children's Hospital, Grupo Hospitalar Conceição, Porto Alegre, RS, Brazil.
  • Ardila DLV; UNIVATES University, Lajeado, RS, Brazil.
  • Alegra T; Department of Genetics, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
  • Pereira TV; Nutrition, Biomarkers and Health Research Group, University College Dublin, Dublin, Ireland.
  • Vairo FPE; Instituto de Educação e Ciências em Saúde, Hospital Alemão Osvaldo Cruz, São Paulo, SP, Brazil.
  • Schwartz IVD; Medical Genetics Service, Hospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brazil.
PLoS One ; 12(8): e0184065, 2017.
Article em En | MEDLINE | ID: mdl-28859139
OBJECTIVE: To evaluate the efficacy and safety of IV laronidase for MPS I. METHODS: A systematic literature review was performed by searching the ClinicalTrials.gov, MEDLINE/PubMed, EMBASE, LILACS, and Cochrane Library databases, limited to clinical trials published until December 31, 2016. The first inclusion criterion was being a randomized controlled trial (RCT). If < five RCTs were identified, open-label and nonrandomized trials, controlled or uncontrolled (quasi-experimental), including ≥ five patients, and evaluating relevant outcomes defined a priori, would also be included. For meta-analysis, primary inferences were based on random-effects models. Assessment of article quality was performed in accordance with the GRADE criteria. The Cochrane Risk of Bias tool was used to examine the risk of bias for RCTs. RESULTS: The selection phase retrieved 632 articles. During the first phase of selection, 158 had the abstract or full text read for assessment of eligibility, of which nine (two RCTs) were included for qualitative synthesis. Four papers were included in the meta-analysis, which was performed for the following outcomes: occurrence of treatment-emergent or infusion-related adverse events (65%; 95%CI 53, 76), mild in most cases; development of IgG antibodies to laronidase (88%; 95%CI 67, 100); apnea-hypopnea index (not significant-NS), urinary glycosaminoglycans (GAGs) [mean change -65.5 µg/mg creatinine (95%CI -68.8, -62.3)], liver size [mean change -31.03% (95%CI -36.1, -25.9)], left ventricular mass index (LVMI) [mean change -1.8 (95%CI -2.32, -0.25)], and distance covered in the 6-minute walk test (NS). Among the outcomes not included in meta-analysis, we found evidence for benefit of laronidase only on shoulder flexion. CONCLUSIONS: Our findings suggest that IV laronidase effectively reduces urinary GAGs excretion, hepatomegaly and LVMI, and can improve shoulder flexion in MPS I patients. Laronidase appears to be safe in the studied population.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mucopolissacaridose I / Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos / Iduronidase Tipo de estudo: Clinical_trials / Prognostic_studies / Qualitative_research / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mucopolissacaridose I / Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos / Iduronidase Tipo de estudo: Clinical_trials / Prognostic_studies / Qualitative_research / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article