Cardio- Renal Outcomes With Long- Term Agalsidase Alfa Enzyme Replacement Therapy: A 10- Year Fabry Outcome Survey (FOS) Analysis

dc.contributor
Institut Català de la Salut
dc.contributor
[Ramaswami U, Hughes D] Royal Free London NHS Foundation Trust, Lysosomal Disorders Unit, Institute of Immunity and Transplantation, London, UK. [Beck M, Kampmann C] Centre for Paediatric and Adolescent Medicine, University Medical Centre, University of Mainz, Mainz, Germany. [Botha J] Department of Biostatistics and Programming, Takeda, Zug, Switzerland. [Pintos-Morell G] Malalties minoritàries, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Research Institute and Teaching Unit Germans Trias i Pujol. Universitat Autònoma de Barcelona, Bellaterra, Spain
dc.contributor
Vall d'Hebron Barcelona Hospital Campus
dc.contributor.author
Ramaswami, Uma
dc.contributor.author
Beck, Michael
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Kampmann, Christoph
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Botha, Jaco
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Pintos Morell, Guillem
dc.contributor.author
Hughes, Derralynn
dc.date.accessioned
2025-10-24T10:25:22Z
dc.date.available
2025-10-24T10:25:22Z
dc.date.issued
2021-04-16T14:31:11Z
dc.date.issued
2021-04-16T14:31:11Z
dc.date.issued
2019-10-25
dc.identifier
Ramaswami U, Beck M, Hughes D, Kampmann C, Botha J, Pintos-Morell G, et al. Cardio-renal outcomes with long-term agalsidase alfa enzyme replacement therapy: A 10-year fabry outcome survey (FOS) analysis. Drug Des Devel Ther. 2019;13:3705–15.
dc.identifier
1177-8881
dc.identifier
https://hdl.handle.net/11351/5871
dc.identifier
10.2147/DDDT.S207856
dc.identifier
31749608
dc.identifier
000492854800001
dc.identifier.uri
https://hdl.handle.net/11351/5871
dc.description.abstract
Agalsidasa alfa; Teràpia de reemplaçament enzimàtic; Malaltia de Fabry
dc.description.abstract
Agalsidasa alfa; Terapia de reemplazo de enzimas; Enfermedad de Fabry
dc.description.abstract
Agalsidase alfa; Enzyme replacement therapy; Fabry disease
dc.description.abstract
Purpose: Following the publication of 5-year agalsidase alfa enzyme replacement therapy (ERT) outcomes data from the Fabry Outcome Survey (FOS), 10-year data were analyzed. Patients and methods: FOS (ClinicalTrials.gov identifier: NCT03289065) data (April 2001 to August 2018) were retrospectively analyzed. Estimated glomerular filtration rate (eGFR) and left ventricular mass indexed to height (LVMI) were analyzed after treatment start (baseline) for patients with ≥3 measurements, including baseline and year 10. Results: Median (range) age (years) of the evaluable treated renal cohort at treatment start was 48.8 (17.9–67.3) for females (n=62), 34.4 (18.0–66.8) for males (n=90). With eGFR ≥60 mL/min/1.73 m2 at baseline, mean (95% CI) rate of eGFR change (eGFR/year) over 10 years was relatively stable in females (n=52; −0.55 [−1.12, +0.01]) and slightly declined in males (n=79; −1.99 [−2.45, −1.54]). With impaired kidney function (eGFR <60 mL/min/1.73 m2) at baseline, mean (95% CI) eGFR/year was stable in females (n=10; −0.14 [−1.43, +1.15]) and slightly declined in males (n=11; −2.79 [−4.01, −1.56]) over 10 years. Median (range) age (years) of the evaluable treated cardiac cohort at treatment start was 46.7 (3.7–67.3) for females (n=34), 28.2 (4.0–54.2) for males (n=35). With left ventricular hypertrophy (LVH; LVMI >48 g/m2.7 in females, >50 g/m2.7 in males) at baseline, mean (95% CI) LVMI/year slightly increased over 10 years in females (n=18; +1.51 [+0.91, +2.12]) and males (n=14; +0.87 (+0.19, +1.55). Without LVH at baseline, mean (95% CI) LVMI/year was stable in females (n=16; +0.52 [−0.13, +1.17]) and males (n=21; +0.57 [+0.02, +1.13]) over 10 years. Conclusion: Agalsidase alfa-treated patients with 10-year FOS data and preserved kidney function and/or normal LVMI at baseline remained largely stable; those with decreased kidney function or LVH at baseline experienced modest declines in renal function and/or increases in LVMI.
dc.description.abstract
The Fabry Outcome Survey is sponsored by Shire Human Genetic Therapies, Inc., a member of the Takeda group of companies. Shire International GmbH, a member of the Takeda group of companies, provided funding to Excel Medical Affairs for support in writing and editing this manuscript and participated in data collection and analysis.
dc.format
application/pdf
dc.language
eng
dc.publisher
Dove Medical Press
dc.relation
Drug Design, Development and Therapy;13
dc.relation
https://www.dovepress.com/cardio--renal-outcomes-with-long--term-agalsidase-alfa-enzyme-replacem-peer-reviewed-article-DDDT
dc.rights
Attribution-NonCommercial 4.0 International
dc.rights
http://creativecommons.org/licenses/by-nc/4.0/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Scientia
dc.subject
Enzims - Regulació
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Malalties congènites
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Metabolisme - Trastorns
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DISEASES::Cardiovascular Diseases::Vascular Diseases::Cerebrovascular Disorders::Cerebral Small Vessel Diseases::Fabry Disease
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ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Therapeutics::Drug Therapy::Enzyme Therapy::Enzyme Replacement Therapy
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ENFERMEDADES::enfermedades cardiovasculares::enfermedades vasculares::trastornos cerebrovasculares::enfermedades de los pequeños vasos cerebrales::enfermedad de Fabry
dc.subject
TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::terapéutica::farmacoterapia::terapia enzimática::tratamiento de sustitución enzimática
dc.title
Cardio- Renal Outcomes With Long- Term Agalsidase Alfa Enzyme Replacement Therapy: A 10- Year Fabry Outcome Survey (FOS) Analysis
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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