Orphanet Journal of Rare Diseases · 2018 · 36 citations · 24 references
PharmacyPharmacologyPharmacotherapyClinical PharmacologyGastroenterologyGastrointestinal PharmacotherapyDiarrhea ManagementDiarrhea PharmacotherapyTranslational BiomarkersBiomarker Clinical UtilityClinical Biomarker AssaysClinical Biomarker ImplementationFabry DiseaseFunctional Gastrointestinal SymptomsGastrointestinal Disease BiomarkersMinimally Important DifferencePatient-reported Symptom Scales
BACKGROUND: Fabry disease is frequently characterized by gastrointestinal symptoms, including diarrhea. Migalastat is an orally-administered small molecule approved to treat the symptoms of Fabry disease in patients with amenable mutations. METHODS: We evaluated minimal clinically important differences (MCID) in diarrhea based on the corresponding domain of the patient-reported Gastrointestinal Symptom Rating Scale (GSRS) in patients with Fabry disease and amenable mutations (N = 50) treated with migalastat 150 mg every other day or placebo during the phase 3 FACETS trial (NCT00925301). RESULTS: After 6 months, significantly more patients receiving migalastat versus placebo experienced improvement in diarrhea based on a MCID of 0.33 (43% vs 11%; p = .02), including the subset with baseline diarrhea (71% vs 20%; p = .02). A decline in kidney peritubular capillary globotriaosylceramide inclusions correlated with diarrhea improvement; patients with a reduction > 0.1 were 5.6 times more likely to have an improvement in diarrhea than those without (p = .031). CONCLUSIONS: Migalastat was associated with a clinically meaningful improvement in diarrhea in patients with Fabry disease and amenable mutations. Reductions in kidney globotriaosylceramide may be a useful surrogate endpoint to predict clinical benefit with migalastat in patients with Fabry disease. TRIAL REGISTRATION: NCT00925301 ; June 19, 2009.
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Károly Kulich, Ahmed Madisch, F. Pacini et al. · Health and Quality of Life Outcomes · 2008 · 395 citations · Full text