Treatment of Duchenne muscular dystrophy with ciclosporin A: a randomised, double-blind, placebo-controlled multicentre trial

التفاصيل البيبلوغرافية
العنوان: Treatment of Duchenne muscular dystrophy with ciclosporin A: a randomised, double-blind, placebo-controlled multicentre trial
المؤلفون: Florian Stehling, Claudia Schmoor, Janbernd Kirschner, G. Bernert, Simone Thiele, Bernd Reitter, Jürg Lütschg, Rudolf Korinthenberg, Gabriele Ihorst, Gert Wiegand, Maja von der Hagen, Ekkehard Wilichowski, Ulrike Schara, Elke Hobbiebrunken, Georg M. Stettner, Ulrike Grieben, Simone Weiss, Joachim Schessl, Wolfgang Müller-Felber
المصدر: The Lancet. Neurology. 9(11)
سنة النشر: 2010
مصطلحات موضوعية: Male, medicine.medical_specialty, Duchenne muscular dystrophy, Medizin, Placebo, law.invention, 03 medical and health sciences, 0302 clinical medicine, Randomized controlled trial, Double-Blind Method, law, Prednisone, Internal medicine, medicine, Humans, Muscular dystrophy, Child, 030304 developmental biology, 0303 health sciences, business.industry, Muscle weakness, medicine.disease, Ciclosporin, 3. Good health, Surgery, Clinical trial, Muscular Dystrophy, Duchenne, Review Literature as Topic, Treatment Outcome, Cyclosporine, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery, medicine.drug
الوصف: Summary Background Duchenne muscular dystrophy is a rare X-linked progressive disease characterised by loss of ambulation at about age 10 years, with death in early adulthood due to respiratory and cardiac insufficiency. Steroids are effective at slowing the progression of muscle weakness; however, their use is limited by side-effects, prompting the search for alternatives. We assessed the effect of ciclosporin A as monotherapy and in combination with intermittent prednisone for the treatment of ambulant patients with this disorder. Methods Our study was a parallel-group, placebo-controlled, double-blind, multicentre trial at trial sites of the German muscular dystrophy network, MD-NET, over 36 months. Ambulant patients with Duchenne muscular dystrophy who were aged 5 years or older were randomly assigned to receive either ciclosporin A (3·5–4·0 mg/kg per day) or matching placebo. Allocation was done centrally with computer-generated random numbers. Patients and investigators were masked to the allocated treatment. After 3 months of treatment, both groups were also given intermittent prednisone for a further 12 months (0·75 mg/kg, alternating 10 days on with 10 days off). All patients who received at least one dose of study drug or placebo were included in the primary analysis. The primary outcome measure was manual muscle strength measured on the Medical Research Council (MRC) scale. This trial is registered with the German clinical trial register DRKS, number DRKS00000445. Findings 77 patients were randomly assigned to the ciclosporin A group and 76 to the placebo group; 73 patients on ciclosporin A and 73 on placebo received at least one dose and were available for efficacy analyses. 3 months of treatment with ciclosporin A alone did not show any significant improvement in primary outcome measures (mean change in the proportion of a possible total MRC score [%MRC] was −2·6 [SD 6·0] for patients on ciclosporin A and −0·8 [4·9] for patients on placebo; adjusted group difference estimate −0·88, 97·5% CI −2·6 to 0·9; p=0·26). The combination of ciclosporin A with intermittent steroids was not better than intermittent steroids alone over 12 months (mean change in %MRC was 0·7 [7·1] for patients on ciclosporin A and −0·3 [7·9] for patients on placebo; adjusted group difference estimate −0·85, −3·6 to 1·9; p=0·48). Numbers of adverse events (75 in patients on ciclosporin A and 74 on placebo) and serious adverse events (four with ciclosporin A and four with placebo) did not differ significantly between groups. Interpretation Ciclosporin A alone or in combination with intermittent prednisone does not improve muscle strength or functional abilities in ambulant boys with Duchenne muscular dystrophy, but is safe and well tolerated. Funding German Federal Ministry of Education and Research, Action Benni and co eV, Novartis Pharma AG, and Deutsche Gesellschaft fur Muskelkranke eV.
تدمد: 1474-4465
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::657a9863efa0614c6516326217a050a6Test
https://pubmed.ncbi.nlm.nih.gov/21087735Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....657a9863efa0614c6516326217a050a6
قاعدة البيانات: OpenAIRE