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Journal of Neurology

, Volume 261, Issue 9, pp 1684–1690 | Cite as

Cessation and resuming of alglucosidase alfa in Pompe disease: a retrospective analysis

  • Thomas HundsbergerEmail author
  • Kai M. Rösler
  • Oliver Findling
Original Communication

Abstract

Enzyme replacement therapy (ERT) with recombinant human alglucosidase alfa (rhGAA) in late-onset Pompe disease is moderately effective. Little is known about the clinical course after treatment termination and the resumption of ERT. In Switzerland, rhGAA therapy for Pompe disease was temporarily withdrawn after the federal court judged that the treatment costs were greatly out of proportion compared to the benefits. Re-treatment was initiated after the therapy was finally licensed. We retrospectively analysed seven Pompe patients, who underwent cessation and resumption of ERT (median age 43 years). The delay from first symptoms to final diagnosis ranged from 4 to 20 years. The demographics, clinical characteristics, assessments with the 6-min walking test (6-MWT), the predicted forced vital capacity (FVC) and muscle strength were analysed. Before initiation of ERT, all patients suffered from proximal muscle weakness of the lower limbs; one was wheelchair-bound and two patients received night-time non-invasive ventilation. Initial treatment stabilised respiratory function in most patients and improved their walking performance. After treatment cessation, upright FVC declined in most and the 6-MWT declined in all patients. Two patients needed additional non-invasive ventilatory support. Twelve months after resuming ERT, the respiratory and walking capacity improved again in most patients. However, aside for one patient, none of the patients reached the same level of respiratory function or distance walked in 6 min, as at the time of ERT withdrawal. We conclude that cessation of ERT in Pompe disease causes a decline in clinical function and should be avoided. Resuming treatment only partially recovers respiratory function and walking capacity.

Keywords

Muscle disease Metabolic disease Pompe disease GSD II Enzyme replacement therapy 

Notes

Acknowledgments

TH thanks Barbara Tettenborn for continuous support for treating patients with Pompe disease.

Conflicts of interest

TH and KMR served as consultants, received funding for travel expenses and received honoraria from serving on a scientific advisory board from Genzyme, Switzerland. OF received funding for trips and received honoraria from serving on a scientific advisory board from Genzyme, Switzerland.

Ethical standards

The local ethics committee approved this retrospective analysis.

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Copyright information

© Springer-Verlag Berlin Heidelberg 2014

Authors and Affiliations

  • Thomas Hundsberger
    • 1
    Email author
  • Kai M. Rösler
    • 2
  • Oliver Findling
    • 2
  1. 1.Department of NeurologyCantonal Hospital St. GallenSt. GallenSwitzerland
  2. 2.Department of NeurologyInselspital, University Hospital Bern and University of BernBernSwitzerland

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