[en] [en] BACKGROUND AND OBJECTIVES: Clinical trials of genotype-targeted treatments in Duchenne muscular dystrophy (DMD) traditionally compare treated patients with untreated patients with the same DMD genotype class. This avoids confounding of drug efficacy by genotype effects but also shrinks the pool of eligible controls, increasing challenges for trial enrollment in this already rare disease. To evaluate the suitability of genotypically unmatched controls in DMD, we quantified effects of genotype class on 1-year changes in motor function endpoints used in clinical trials.
METHODS: More than 1,600 patient-years of follow-up (>700 patients) were studied from 6 real-world/natural history data sources (UZ Leuven, PRO-DMD-01 shared by CureDuchenne, iMDEX, North Star UK, Cincinnati Children's Hospital Medical Center, and the DMD Italian Group), with genotypes classified as amenable to skipping exons 44, 45, 51, or 53, or other skippable, nonsense, and other mutations. Associations between genotype class and 1-year changes in North Star Ambulatory Assessment total score (ΔNSAA) and in 10-m walk/run velocity (Δ10MWR) were studied in each data source with and without adjustment for baseline prognostic factors.
RESULTS: The studied genotype classes accounted for approximately 2% of variation in ΔNSAA outcomes after 12 months, whereas other prognostic factors explained >30% of variation in large data sources. Based on a meta-analysis across all data sources, pooled effect estimates for the studied skip-amenable mutation classes were all small in magnitude (<2 units in ΔNSAA total score in 1-year follow up), smaller than clinically important differences in NSAA, and were precisely estimated with standard errors <1 unit after adjusting for nongenotypic prognostic factors.
DISCUSSION: These findings suggest the viability of trial designs incorporating genotypically mixed or unmatched controls for up to 12 months in duration for motor function outcomes, which would ease recruitment challenges and reduce numbers of patients assigned to placebos. Such trial designs, including multigenotype platform trials and hybrid designs, should ensure baseline balance between treatment and control groups for the most important prognostic factors, while accounting for small remaining genotype effects quantified in this study.
Disciplines :
Pediatrics
Author, co-author :
Muntoni, Francesco ; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands
Signorovitch, James; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands. james.signorovitch@analysisgroup.com
Sajeev, Gautam ; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands
Lane, Henry; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands
Jenkins, Madeline; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands
Dieye, Ibrahima; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands
Ward, Susan J; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands
McDonald, Craig; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands
Goemans, Nathalie ; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands
Niks, Erik H ; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands
Wong, Brenda; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands
Servais, Laurent ; Université de Liège - ULiège > Département des sciences cliniques
Straub, Volker ; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands
Guglieri, Michela; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands
de Groot, Imelda J M; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands
Chesshyre, Mary; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands
Tian, Cuixia; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands
Manzur, Adnan Y; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands
Mercuri, Eugenio; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands
Aartsma-Rus, Annemieke; From the Dubowitz Neuromuscular Centre (F.M., M.C., A.Y.M.), NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, and Great Ormond Street Hospital Trust, United Kingdom, Analysis Group, Inc. (J.S., G.S., H.L., M.J., I.D.), Boston, The Collaborative Trajectory Analysis Project (J.S., S.J.W.), Cambridge, MA, Department of Physical Medicine and Rehabilitation, and Pediatrics (C.M.), University of California, Davis, Sacramento, Child Neurology (N.G.), University Hospitals Leuven, Belgium, Department of Neurology (E.H.N.), Leiden University Medical Centre, the Netherlands, Department of Pediatrics (B.W.), University of Massachusetts Medical School, Worcester, MDUK Oxford Neuromuscular Center (L.S.), Department of Paediatrics, University of Oxford, United Kingdom and Neuromuscular Center of Liège (L.S.), Division of Paediatrics, CHU and University of Liège, Belgium, John Walton Muscular Dystrophy Research Centre (V.S., M.G.), Newcastle University and Newcastle Hospitals NHS Foundation Trust, United Kingdom, Department of Rehabilitation (I.J.M.d.G.), Donders Centre of Neuroscience, Radboud University Nijmegen Medical Center, the Netherlands, Cincinnati Children's Hospital Medical Center (C.T.), and College of Medicine (C.T.), University of Cincinnati, OH, Department of Pediatric Neurology (E.M.), Fondazione Policlinico Gemelli IRCCS, Catholic University, Rome, Italy, and Department of Human Genetics (A.A.-R.), Leiden University Medical Center, the Netherlands
Association Française Contre Les Myopathies; on behalf of Universitaire Ziekenhuizen Leuven Group, PRO-DMD-01, The UK NorthStar Clinical Network, CCHMC, and The DMD Italian Group
Emery A, Muntoni F, Quinlivan R. Duchenne Muscular Dystrophy, 4th ed. Oxford University Press, 2015.
Mah JK, Korngut L, Fiest KM, et al. A systematic review and meta-analysis on the epidemiology of the muscular dystrophies. Can J Neurol Sci. 2016;43(1):163-177. doi: 10.1017/cjn.2015.311.
Aartsma-Rus A, Van Deutekom JCT, Fokkema IF, Van Ommen GJB, Den Dunnen JT. Entries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule. Muscle Nerve. 2006;34(2):135-144. doi:10.1002/mus.20586.
Bladen CL, Salgado D, Monges S, et al. The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations. Hum Mutat. 2015;36(4):395-402. doi:10.1002/humu.22758.
Duan D, Goemans N, Takeda S, Mercuri E, Aartsma-Rus A. Duchenne muscular dystrophy. Nat Rev Dis Primers. 2021;7(1):13. doi:10.1038/s41572-021-00248-3.
National Institute of Neurological Disorders and Stroke (NINDS). Muscular Dystrophy Information. Accessed April 8, 2022. ninds.nih.gov/Disorders/All-Disorders/ Muscular-Dystrophy-Information-Page.
Bello L, Morgenroth LP, Gordish-Dressman H, Hoffman EP, McDonald CM, Cirak S. DMD genotypes and loss of ambulation in the CINRG Duchenne Natural History Study. Neurology. 2016;87(4):401-409. doi:10.1212/wnl.0000000000002891.
Ricotti V, Evans MRB, Sinclair CDJ, et al. Upper limb evaluation in Duchenne muscular dystrophy: fat-water quantification by MRI, muscle force and function define endpoints for clinical trials. PLoS One. 2016;11(9):e0162542. doi:10.1371/ journal.pone.0162542.
Birnkrant DJ, Bushby K, Bann CM, et al. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management. Lancet Neurol. 2018;17(3):251-267. doi:10.1016/s1474-4422(18)30024-3.
Birnkrant DJ, Bushby K, Bann CM, et al. Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic management. Lancet Neurol. 2018;17(4):347-361. doi:10.1016/s1474-4422(18)30025-5.
Birnkrant DJ, Bushby K, Bann CM, et al. Diagnosis and management of Duchenne muscular dystrophy, part 3: primary care, emergency management, psychosocial care, and transitions of care across the lifespan. Lancet Neurol. 2018;17(5):445-455. doi: 10.1016/s1474-4422(18)30026-7.
McDonald CM, Campbell C, Torricelli RE, et al. Ataluren in patients with nonsense mutation Duchenne muscular dystrophy (ACT DMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial. Lancet. 2017;390(10101):1489-1498. doi:10.1016/S0140-6736(17)31611-2.
Nakamura A, Shiba N, Miyazaki D, et al. Comparison of the phenotypes of patients harboring in-frame deletions starting at exon 45 in the Duchenne muscular dystrophy gene indicates potential for the development of exon skipping therapy. J Hum Genet. 2017;62(4):459-463. doi:10.1038/jhg.2016.152.
Charleston JS, Schnell FJ, Dworzak J, et al. Eteplirsen treatment for Duchenne muscular dystrophy: exon skipping and dystrophin production. Neurology. 2018; 90(24):e2146-e2154. doi:10.1212/wnl.0000000000005680.
Clemens PR, Rao VK, Connolly AM, et al. Safety, tolerability, and efficacy of viltolarsen in boys with Duchenne muscular dystrophy amenable to exon 53 skipping: a phase 2 randomized clinical trial. JAMA Neurol. 2020;77(8):982-991. doi:10.1001/ jamaneurol.2020.1264.
Frank DE, Schnell FJ, Akana C, et al. Increased dystrophin production with golodirsen in patients with Duchenne muscular dystrophy. Neurology. 2020;94(21): e2270-e2282. doi:10.1212/wnl.0000000000009233.
Wagner KR, Kuntz NL, Koenig E, et al. Safety, tolerability, and pharmacokinetics of casimersen in patients with Duchenne muscular dystrophy amenable to exon 45 skipping: a randomized, double-blind, placebo-controlled, dose-titration trial. Muscle Nerve. 2021;64(3):285-292. doi:10.1002/mus.27347.
Wilton-Clark H, Yokota T. Casimersen for Duchenne muscular dystrophy. Drugs Today (Barc). 2021;57(12):707-717. doi:10.1358/dot.2021.57.12.3352740.
Mendell JR, Goemans N, Lowes LP, et al. Longitudinal effect of eteplirsen versus historical control on ambulation in Duchenne muscular dystrophy. Ann Neurol. 2016; 79(2):257-271. doi:10.1002/ana.24555.
Servais L, Mercuri E, Straub V, et al. Long-term safety and efficacy data of golodirsen in ambulatory patients with duchenne muscular dystrophy amenable to exon 53 skipping: a first-in-human, multicenter, two-part, open-label, phase 1/2 trial. Nucleic Acid Ther. 2022;32(1):29-39. doi:10.1089/nat.2021.0043.
Olson EN. Toward the correction of muscular dystrophy by gene editing. Proc Natl Acad Sci USA. 2021;118(22):e2004840117. doi:10.1073/pnas.2004840117.
Coratti G, Pane M, Brogna C, et al. North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: a 3 year follow up. PLoS One. 2021;16(6):e0253882. doi:10.1371/journal.pone.0253882.
Ricotti V, Ridout DA, Pane M, et al. The NorthStar Ambulatory Assessment in Duchenne muscular dystrophy: considerations for the design of clinical trials. J Neurol Neurosurg Psychiatry. 2016;87(2):149-155. doi:10.1136/jnnp-2014-309405.
Trucco F, Ridout D, Domingos J, et al. Genotype-related respiratory progression in Duchenne muscular dystrophy: a multicenter international study. Muscle Nerve. 2022; 65(1):67-74. doi:10.1002/mus.27427.
Zhang S, Qin D, Wu L, et al. Genotype characterization and delayed loss of ambulation by glucocorticoids in a large cohort of patients with Duchenne muscular dystrophy. Orphanet J Rare Dis. 2021;16(1):188. doi:10.1186/s13023-021-01837-x.
Brogna C, Coratti G, Pane M, et al. Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53. PLoS One. 2019;14(6):e0218683. doi:10.1371/journal.pone.0218683.
Brogna C, Coratt G, Pane M, et al. Correction: long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53. PLoS One. 2019;14(7):e0220714. doi:10.1371/ journal.pone.0220714.
Aartsma-Rus A, Fokkema I, Verschuuren J, et al. Theoretic applicability of antisense-mediated exon skipping for Duchenne muscular dystrophy mutations. Hum Mutat. 2009;30(3):293-299. doi:10.1002/humu.20918.
Fletcher S, Adams AM, Johnsen RD, Greer K, Moulton HM, Wilton SD. Dystrophin isoform induction in vivo by antisense-mediated alternative splicing. Mol Ther. 2010; 18(6):1218-1223. doi:10.1038/mt.2010.45.
Goemans N, Signorovitch J, McDonald C, et al. Functional trajectories of upper limb and pulmonary function before and after loss of ambulation in Duchenne muscular dystrophy. Paper presented at: Muscular Dystrophy Association Clinical & Scientific Conference; June–August 2020. Accessed June–August, 2020. https://www.mda.org/conferences/virtual-conference-hub
McDonald CM, Henricson EK, Abresch RT, et al. The 6-minute walk test and other endpoints in Duchenne muscular dystrophy: longitudinal natural history observations over 48 weeks from a multicenter study. Muscle Nerve. 2013;48(3):343-356. doi: 10.1002/mus.23902.
Scott E, Eagle M, Mayhew A, et al. Development of a functional assessment scale for ambulatory boys with Duchenne muscular dystrophy. Physiother Res Int. 2012;17(2): 101-109. doi:10.1002/pri.520.
Mazzone ES, Messina S, Vasco G, et al. Reliability of the North Star Ambulatory Assessment in a multicentric setting. Neuromuscul Disord. 2009;19(7):458-461. doi: 10.1016/j.nmd.2009.06.368.
Zeger SL, Liang KY, Albert PS. Models for longitudinal data: a generalized estimating equation approach. Biometrics. 1988;44(4):1049-1060. doi:10.2307/2531734.
Goemans N, Vanden Hauwe M, Signorovitch J, Swallow E, Song J. Individualized prediction of changes in 6-minute walk distance for patients with Duchenne muscular dystrophy. PLoS One. 2016;11(10):e0164684. doi:10.1371/journal.pone.0164684.
Wang RT, Barthelemy F, Martin AS, et al. DMD genotype correlations from the Duchenne Registry: endogenous exon skipping is a factor in prolonged ambulation for individuals with a defined mutation subtype. Hum Mutat. 2018;39(9):1193-1202. doi: 10.1002/humu.23561.
Counterman KJ, Furlong P, Wang RT, Martin AS. Delays in diagnosis of Duchenne muscular dystrophy: an evaluation of genotypic and sociodemographic factors. Muscle Nerve. 2020;61(1):36-43. doi:10.1002/mus.26720.
Wong B, Signorovitch J, Staunton H, et al. P.196 Estimating clinically meaningful change thresholds in the NORTH STAR ambolatory assessment (NSAA) and four-stair climb (4SC) in Duchenne muscular dystrophy (DMD). Neuromuscul Disord. 2019;29(suppl 1):S106. doi:10.1016/j.nmd.2019.06.251.
Goemans N, Wong B, Van den Hauwe M, et al. Prognostic factors for changes in the timed 4-stair climb in patients with Duchenne muscular dystrophy, and implications for measuring drug efficacy: a multi-institutional collaboration. PLoS One. 2020; 15(6):e0232870. doi:10.1371/journal.pone.0232870.
Muntoni F, Signorovitch J, Sajeev G, et al. Real-world and natural history data for drug evaluation in Duchenne muscular dystrophy: suitability of the North Star Ambulatory Assessment for comparisons with external controls. Neuromuscul Disord. 2022;32(4): 271-283. doi:10.1016/j.nmd.2022.02.009.
European Medicines Agency. Guideline on adjustment for baseline covariates in clinical trials. 2015:1-11.
Bello L, Kesari A, Gordish-Dressman H, et al. Genetic modifiers of ambulation in the Cooperative International Neuromuscular Research Group Duchenne Natural History Study. Ann Neurol. 2015;77(4):684-696. doi:10.1002/ana.24370.
Bello L, Pegoraro E. The “usual suspects”: genes for inflammation, fibrosis, regeneration, and muscle strength modify Duchenne muscular dystrophy. J Clin Med. 2019;8(5):649. doi:10.3390/jcm8050649.
Chesshyre M, Ridout D, Hashimoto Y, et al. Investigating the role of dystrophin isoform deficiency in motor function in Duchenne muscular dystrophy. J Cachexia Sarcopenia Muscle. 2022;13(2):1360-1372. doi:10.1002/jcsm.12914.
The Adaptive Platform Trials Coalition. Adaptive platform trials: definition, design, conduct and reporting considerations. Nat Rev Drug Discov. 2019;18(10):797-807. doi:10.1038/s41573-019-0034-3.
Park JJH, Siden E, Zoratti MJ, et al. Systematic review of basket trials, umbrella trials, and platform trials: a landscape analysis of master protocols. Trials. 2019;20(1):572. doi:10.1186/s13063-019-3664-1.
Bronson A, Connor E, Duong T, et al. A platform trial for Duchenne muscular dystrophy (DMD): an innovative, patient centric trial to broaden inclusion criteria and speed results. Paper presented at: Muscular Dystrophy Association Clinical & Scientific Conference; June–August 2020. Accessed June–August, 2020. https://www.mda.org/conferences/virtual-conference-hub
VanderWeele TJ, Ding P. Sensitivity analysis in observational research: introducing the E-value. Ann Intern Med. 2017;167(4):268-274. doi:10.7326/m16-2607.
Goemans N, Signorovitch J, Sajeev G, et al. Suitability of external controls for drug evaluation in Duchenne muscular dystrophy. Neurology. 2020;95(10):e1381-e1391. doi:10.1212/wnl.0000000000010170.