Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2013 Feb 19:8:29.
doi: 10.1186/1750-1172-8-29.

Cost-effectiveness of enzyme replacement therapy for Fabry disease

Affiliations

Cost-effectiveness of enzyme replacement therapy for Fabry disease

Saskia M Rombach et al. Orphanet J Rare Dis. .

Abstract

Background: The cost-effectiveness of enzyme replacement therapy (ERT) compared to standard medical care was evaluated in the Dutch cohort of patients with Fabry disease.

Methods: Cost-effectiveness analysis was performed using a life-time state-transition model. Transition probabilities, effectiveness data and costs were derived from retrospective data and prospective follow-up of the Dutch study cohort consisting of males and females aged 5-78 years. Intervention with ERT (either agalsidase alfa or agalsidase beta) was compared to the standard medical care. The main outcome measures were years without end organ damage (renal, cardiac en cerebrovascular complications), quality adjusted life years (QALYs), and costs.

Results: Over a 70 year lifetime, an untreated Fabry patient will generate 55.0 years free of end-organ damage (53.5 years in males, 56.9 years in females) and 48.6 QALYs (47.8 in males, 49.7 in females). Starting ERT in a symptomatic patient increases the number of years free of end-organ damage by 1.5 year (1.6 in males, 1.3 in females), while the number of QALYs gained increases by a similar amount (1.7 in males, 1.4 in females). The costs of ERT starting in the symptomatic stage are between €9 - €10 million (£ 7.9 - £ 8.8 million, $13.0- $14.5 million) during a patient's lifetime. Consequently, the extra costs per additional year free of end-organ damage and the extra costs per additional QALY range from €5.5 - €7.5 million (£ 4.8 - £ 6.6 million, $ 8.0 - $ 10.8 million), undiscounted.

Conclusions: In symptomatic patients with Fabry disease, ERT has limited effect on quality of life and progression to end organ damage. The pharmaco-economic evaluation shows that this modest effectiveness drives the costs per QALY and the costs per year free of end-organ damage to millions of euros. Differentiation of patients who may benefit from ERT should be improved to enhance cost-effectiveness.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Cost-effectiveness acceptability curves of ERT versus no treatment for various levels of willingness-to-pay per QALY after 1,000 runs in a Monte Carlo simulation of beta-distributed state transition probabilities. The proportions of net monetary benefits larger than zero for these willingness-to-pay levels represent the probabilities of ERT being cost-effective in comparison with standard medical care and are reported in the cost-effectiveness acceptability curve.

Similar articles

Cited by

References

    1. Hwu WL, Chien YH, Lee NC, Chiang SC, Dobrovolny R, Huang AC. Newborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset GLA mutation c.936+919 G>A (IVS4+919 G>A) Hum Mutat. 2009;30(10):1397–1405. doi: 10.1002/humu.21074. - DOI - PMC - PubMed
    1. Spada M, Pagliardini S, Yasuda M, Tukel T, Thiagarajan G, Sakuraba H. High incidence of later-onset fabry disease revealed by newborn screening. Am J Hum Genet. 2006;79(1):31–40. doi: 10.1086/504601. - DOI - PMC - PubMed
    1. Desnick RJ, Ioannou YA, Eng CM. In: The metabolic and molecular bases of inherited disease,Volume 3. 8. Scriver CR, Beaudet AL, Sly WS, Valle D, editor. 2001. alpha-Galactosidase A deficiency: Fabry disease; pp. 3733–3774.
    1. MacDermot KD, Holmes A, Miners AH. Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 60 obligate carrier females. J Med Genet. 2001;38(11):769–775. doi: 10.1136/jmg.38.11.769. - DOI - PMC - PubMed
    1. Whybra C, Kampmann C, Willers I, Davies J, Winchester B, Kriegsmann J. Anderson-Fabry disease: clinical manifestations of disease in female heterozygotes. J Inherit Metab Dis. 2001;24(7):715–724. doi: 10.1023/A:1012993305223. - DOI - PubMed

Publication types