Weekly enzyme replacement therapy may slow decline of renal function in patients with Fabry disease who are on long-term biweekly dosing

Raphael Schiffmann, Hasan Askari, Margaret Timmons, Chevalia Robinson, William Benko, Roscoe O. Brady, Markus Ries

Research output: Contribution to journalArticle

107 Citations (Scopus)

Abstract

This study was performed to determine whether adult male patients with Fabry disease who demonstrate a continuing decline in renal function despite 2 to 4 yr of conventionally dosed agalsidase alfa therapy (0.2 mg/kg every other week [EOW]) show an improved slope of decline with weekly administration using the same dosage. Eleven (27%) of 41 adult male patients with Fabry disease who participated in long-term agalsidase alfa clinical trials and who had demonstrated a slope of decline in estimated GFR (eGFR) of ≥5 ml/min per 1.73 m2/yr while receiving long-term treatment with agalsidase alfa at the currently recommended dosage of 0.2 mg/kg, infused EOW, were enrolled in this open-label, prospective study. Patients were switched from EOW to weekly infusions and followed for an additional 24 mo. Before switching to weekly dosing, eGFR was 53.7 ± 6.3 ml/min per 1.73 m2 (mean ± SEM), and mean rate of change in eGFR was -8.0 ± 0.8 ml/min per 1.73 m2/yr. During the 24-mo follow-up period after switching to weekly dosing, the mean rate of change in eGFR was observed to slow to -3.3 ± 1.4 ml/min/1.73 m2/yr (P = 0.01 versus EOW). After switching to weekly dosing, three patients demonstrated an improvement in eGFR and six patients demonstrated a slowing in the rate of eGFR decline; only two patients failed to improve their eGFR slope. A multiple regression model confirmed that the weekly infusion regimen was the strongest explanatory variable for the change in eGFR (P = 0.0008), with a weaker contribution from the concomitant use of angiotensin converting enzyme inhibitors/angiotensin receptor blockers (P = 0.02). These results suggest that weekly infusions of agalsidase alfa at a dosage of 0.2 mg/kg may be beneficial in the subgroup of patients who have Fabry disease and whose kidney function continues to decline after 2 to 4 yr or more of standard EOW dosing.

Original languageEnglish (US)
Pages (from-to)1576-1583
Number of pages8
JournalJournal of the American Society of Nephrology
Volume18
Issue number5
DOIs
StatePublished - May 1 2007
Externally publishedYes

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Enzyme Replacement Therapy
Fabry Disease
Kidney
Angiotensin Receptor Antagonists
Angiotensin-Converting Enzyme Inhibitors
Clinical Trials
Prospective Studies
agalsidase alfa
Therapeutics

ASJC Scopus subject areas

  • Nephrology

Cite this

Weekly enzyme replacement therapy may slow decline of renal function in patients with Fabry disease who are on long-term biweekly dosing. / Schiffmann, Raphael; Askari, Hasan; Timmons, Margaret; Robinson, Chevalia; Benko, William; Brady, Roscoe O.; Ries, Markus.

In: Journal of the American Society of Nephrology, Vol. 18, No. 5, 01.05.2007, p. 1576-1583.

Research output: Contribution to journalArticle

Schiffmann, Raphael ; Askari, Hasan ; Timmons, Margaret ; Robinson, Chevalia ; Benko, William ; Brady, Roscoe O. ; Ries, Markus. / Weekly enzyme replacement therapy may slow decline of renal function in patients with Fabry disease who are on long-term biweekly dosing. In: Journal of the American Society of Nephrology. 2007 ; Vol. 18, No. 5. pp. 1576-1583.
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