Meta-analyses of deflazacort versus prednisone/prednisolone in patients with nonsense mutation Duchenne muscular dystrophy
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Published:2021-12
Issue:18
Volume:10
Page:1337-1347
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ISSN:2042-6305
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Container-title:Journal of Comparative Effectiveness Research
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language:en
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Short-container-title:Journal of Comparative Effectiveness Research
Author:
Shieh Perry B1ORCID, Elfring Gary2, Trifillis Panayiota2, Santos Claudio2, Peltz Stuart W2, Parsons Julie A3, Apkon Susan3, Darras Basil T4, Campbell Craig5, McDonald Craig M6ORCID, Barohn Richard J, Bertini Enrico, Bushby Kate, Chabrol Brigitte, Ciafaloni Emma, Columer Jaume, Comi Giacomi Pietro, Connolly Anne, Finkel Richard S, Flanigan Kevin M, Goemans Nathalie, Guglieri Michela, Iannaccone Susan T, Jones Kristi J, Kaufmann Petra, Kirschner Janbernd, Mah Jean K, Mathews Katherine, Mercuri Eugenio, Muntoni Francesco, Nevo Yoram, Osorio Andrés Nascimento, Péréon Yann, Quinlivan Rosaline, Renfroe J. Ben, Russman Barry, Ryan Monique, Sampson Jacinda, Schara Ulrike, Selby Kathryn, Sejersen Thomas, Sproule Douglas M, Sweeney H. Lee, Tulinius Már, Vilchez Juan J, Vita Giuseppe, Voit Thomas, Burns-Wechsler Stephanie, Wong Brenda, Abresch Ted, Henricson Erik K, Coleman Kim, Eagle Michelle, Florence Julaine, Gappmaier Ed, McDonald Craig, Abdel-Hamid Hoda Z, Barohn Richard J, Bertini Enrico, Bloetzer Clemens, Bushby Kate, Butterfield Russell J, Chabrol Brigitte, Chae Jong-Hee, Comi Giacomi Pietro, Dastgir Jahannaz, Desguerre Isabelle, Escobar Raul G, Finanger Erika, Finkel Richard S, Flanigan Kevin M, Goemans Nathalie, Guglieri Michela, Heydemann Peter, Hughes Imelda, Iannaccone Susan T, Jones Kristi J, Kaminska Anna, Karachunski Peter, Kirschner Janbernd, Kudr Martin, Lotze Timothy, Mah Jean K, Mathews Katherine, Mercuri Eugenio, Muntoni Francesco, Nevo Yoram, Osorio Andrés Nascimento, Péréon Yann, de Queiroz Campos Araujo Alexandra Prufer, Renfroe J. Ben, Dutra de Resende Maria Bernadete, Ryan Monique, Sampson Jacinda, Schara Ulrike, Selby Kathryn, Sejersen Thomas, Sweeney H. Lee, Tennekoon Gihan, Topaloglu Haluk, Torricelli Ricardo Erazo, Tulinius Már, Vilchez Juan J, Vita Giuseppe, Voit Thomas, Wong Brenda, Alfano Lindsay N, Eagle Michelle, James Meredith K, Lowes Linda, Mayhew Anna, Mazzone Elena S, Nelson Leslie, Rose Kristy J
Affiliation:
1. University of California at Los Angeles, Los Angeles, CA, USA 2. PTC Therapeutics, Inc., South Plainfield, NJ, USA 3. University of Colorado School of Medicine, Aurora, CO, USA 4. Boston Children’s Hospital, Boston, MA, USA 5. Children’s Hospital – London Health Sciences Centre, University of Western Ontario, London, ON, Canada 6. University of California Davis Health, Sacramento, CA, USA
Abstract
Aim: Compare efficacies of deflazacort and prednisone/prednisolone in providing clinically meaningful delays in loss of physical milestones in patients with nonsense mutation Duchenne muscular dystrophy. Materials & methods: Placebo data from Phase IIb (ClinicalTrials.gov Identifier: NCT00592553) and ACT DMD (ClinicalTrials.gov Identifier: NCT01826487) ataluren nonsense mutation Duchenne muscular dystrophy clinical trials were retrospectively combined in meta-analyses (intent-to-treat population; for change from baseline to week 48 in 6-min walk distance [6MWD] and timed function tests). Results: Significant improvements in change in 6-min walk distance with deflazacort versus prednisone/prednisolone (least-squares mean difference 39.54 m [95% CI: 13.799, 65.286; p = 0.0026]). Significant and clinically meaningful improvements in 4-stair climb and 4-stair descend for deflazacort versus prednisone/prednisolone. Conclusion: Deflazacort provides clinically meaningful delays in loss of physical milestones over 48 weeks compared with prednisone/prednisolone for patients with nonsense mutation Duchenne muscular dystrophy.
Publisher
Future Medicine Ltd
Reference33 articles.
1. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management 2. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management 3. Diagnosis and management of Duchenne muscular dystrophy, part 3: primary care, emergency management, psychosocial care, and transitions of care across the lifespan 4. Long-term effects of glucocorticoids on function, quality of life, and survival in patients with Duchenne muscular dystrophy: a prospective cohort study 5. Practice guideline update summary: Corticosteroid treatment of Duchenne muscular dystrophy
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