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Clinical Trial
. 2007 May;18(5):1576-83.
doi: 10.1681/ASN.2006111263. Epub 2007 Apr 4.

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

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Clinical Trial

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

Raphael Schiffmann et al. J Am Soc Nephrol. 2007 May.

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 > or =5 ml/min per 1.73 m(2)/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 m(2) (mean +/- SEM), and mean rate of change in eGFR was -8.0 +/- 0.8 ml/min per 1.73 m(2)/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 m(2)/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.

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Figures

Figure 1
Figure 1
The effect of changing the dosing frequency of agalsidase alfa from every other week (EOW) to weekly in patients whose estimated GFR (eGFR) declines at >5 ml/min per 1.73 m2/yr during long-term EOW therapy. Each symbol represent an individual patient, and the squares represent the mean ± SEM during EOW and weekly dosing.
Figure 2
Figure 2
Effect of EOW and weekly agalsidase alfa treatment on urinary protein excretion. The individual symbols represent the same patients depicted in Figure 1.
Figure 3
Figure 3
The effect of EOW and weekly agalsidase alfa on urine sediment globotriaosylceramide (Gb3) in male patients with Fabry disease. Pre indicates value before the start of EOW dosing. The individual symbols represent the same patients depicted in Figure 1.

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References

    1. Brady R, Gal AE, Bradley RM, Martensson E, Warshaw AL, Laster L. Enzymatic defect in Fabry’s disease. Ceramidetrihexosidase deficiency. N Engl J Med. 1967;276:1163–1167. - PubMed
    1. Brady RO, Schiffmann R. Clinical features of and recent advances in therapy for Fabry disease. JAMA. 2000;284:2771–2775. - PubMed
    1. Meikle PJ, Hopwood JJ, Clague AE, Carey WF. Prevalence of lysosomal storage disorders. JAMA. 1999;281:249–254. - PubMed
    1. Ries M, Moore DF, Robinson CJ, Tifft CJ, Rosenbaum KN, Brady RO, Schiffmann R, Krasnewich D. Quantitative dys-morphology assessment in Fabry disease. Genet Med. 2006;8:96–101. - PubMed
    1. Ries M, Ramaswami U, Parini R, Lindblad B, Whybra C, Willers I, Gal A, Beck M. The early clinical phenotype of Fabry disease: A study on 35 European children and adolescents. Eur J Pediatr. 2003;162:767–772. - PubMed

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