Literature DB >> 19287243

Clinical outcomes after long-term treatment with alglucosidase alfa in infants and children with advanced Pompe disease.

Marc Nicolino1, Barry Byrne, J Edmund Wraith, Nancy Leslie, Hanna Mandel, David R Freyer, Georgianne L Arnold, Eniko K Pivnick, C J Ottinger, Peter H Robinson, John-Charles A Loo, Martin Smitka, Philip Jardine, Luciano Tatò, Brigitte Chabrol, Shawn McCandless, Shigemi Kimura, L Mehta, Deeksha Bali, Alison Skrinar, Claire Morgan, Lakshmi Rangachari, Deya Corzo, Priya S Kishnani.   

Abstract

PURPOSE: A clinical trial was conducted to evaluate the safety and efficacy of alglucosidase alfa in infants and children with advanced Pompe disease.
METHODS: Open-label, multicenter study of IV alglucosidase alfa treatment in 21 infants 3-43 months old (median 13 months) with minimal acid alpha-glucosidase activity and abnormal left ventricular mass index by echocardiography. Patients received IV alglucosidase alfa every 2 weeks for up to 168 weeks (median 120 weeks). Survival results were compared with an untreated reference cohort.
RESULTS: At study end, 71% (15/21) of patients were alive and 44% (7/16) of invasive-ventilator free patients remained so. Compared with the untreated reference cohort, alglucosidase alfa reduced the risk of death by 79% (P < 0.001) and the risk of invasive ventilation by 58% (P = 0.02). Left ventricular mass index improved or remained normal in all patients evaluated beyond 12 weeks; 62% (13/21) achieved new motor milestones. Five patients were walking independently at the end of the study and 86% (18/21) gained functional independence skills. Overall, 52% (11/21) of patients experienced infusion-associated reactions; 95% (19/20) developed IgG antibodies to recombinant human lysosomal acid alpha-glucosidase; no patients withdrew from the study because of safety concerns.
CONCLUSIONS: In this population of infants with advanced disease, biweekly infusions with alglucosidase alfa prolonged survival and invasive ventilation-free survival. Treatment also improved indices of cardiomyopathy, motor skills, and functional independence.

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Year:  2009        PMID: 19287243     DOI: 10.1097/GIM.0b013e31819d0996

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  117 in total

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7.  Atypical immunologic response in a patient with CRIM-negative Pompe disease.

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9.  Cross-reactive immunologic material status affects treatment outcomes in Pompe disease infants.

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10.  Response of 33 UK patients with infantile-onset Pompe disease to enzyme replacement therapy.

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