Clinical outcomes in patients switching from agalsidase beta to migalastat: A Fabry Registry analysis

J Inherit Metab Dis. 2024 Sep;47(5):1080-1095. doi: 10.1002/jimd.12773. Epub 2024 Jul 4.

Abstract

Fabry Registry data were analyzed among 83 agalsidase beta-treated patients with Fabry disease who switched to migalastat. Outcomes (estimated glomerular filtration rate [eGFR], urine protein-creatinine ratio [UPCR], plasma globotriaosylceramide [GL-3], plasma globotriaosylsphingosine [lyso-GL-3], interventricular septal wall thickness [IVST], left posterior wall thickness [LPWT], left ventricular mass index [LVMI]) were assessed using linear mixed models to estimate annual change over time in the pre- and postswitch periods. eGFR decreased throughout both periods (preswitch: -0.85 mL/min/1.73 m2/year; postswitch: -1.96 mL/min/1.73 m2/year; both p < 0.0001), with steeper decline postswitch (ppre/post = 0.01) in both classic and late-onset patients. UPCR increased significantly postswitch (ppre/post = 0.003) among classic patients and was stable in both periods among late-onset patients. GL-3 trajectories worsened postswitch across phenotypes (ppre/post = 0.0005 classic, 0.02 late-onset). LPWT was stable preswitch (0.07 mm/year, p = 0.25) and decreased postswitch (-0.51 mm/year, p = 0.0005; ppre/post = 0.0009), primarily among late-onset patients. IVST and LVMI slopes varied significantly by phenotype. Among classic patients, IVST and LVMI were stable and decreasing, respectively preswitch and increasing postswitch (ppre/post = 0.02 IVST, 0.01 LVMI). Among late-onset patients, IVST significantly decreased postswitch (ppre/post = 0.0003); LVMI was stable over time (ppre/post = 0.89). Ultimately, eGFR and GL-3 trajectories worsened postswitch across phenotypes, while UPCR and cardiac measures worsened among classic and stabilized/improved among late-onset patients. These findings indicate variability in long-term outcomes after switching from ERT to migalastat, underscoring the importance of careful monitoring.

Keywords: Fabry disease; agalsidase beta; chaperone; enzyme replacement therapy (ERT); migalastat.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Deoxynojirimycin* / administration & dosage
  • 1-Deoxynojirimycin* / analogs & derivatives
  • 1-Deoxynojirimycin* / therapeutic use
  • Adolescent
  • Adult
  • Enzyme Replacement Therapy / methods
  • Fabry Disease* / drug therapy
  • Female
  • Glomerular Filtration Rate*
  • Glycolipids
  • Humans
  • Isoenzymes* / therapeutic use
  • Male
  • Middle Aged
  • Registries*
  • Sphingolipids / blood
  • Treatment Outcome
  • Trihexosylceramides / metabolism
  • Young Adult
  • alpha-Galactosidase* / therapeutic use

Substances

  • 1-Deoxynojirimycin
  • agalsidase beta
  • migalastat
  • alpha-Galactosidase
  • Isoenzymes
  • globotriaosylceramide
  • Trihexosylceramides
  • globotriaosyl lysosphingolipid
  • Sphingolipids
  • Glycolipids

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