Steroid switching in dystrophinopathy treatment: a US chart review of patient characteristics and clinical outcomes

Author:

Marden Jessica R1ORCID,Santos Claudio2,Pfister Brian2,Able Richard2,Lane Henry1,Somma Michael1,Zhao Jing1,Signorovitch James1,Parsons Julie3,Apkon Susan3

Affiliation:

1. Analysis Group, Inc., Boston, MA 02199, USA

2. PTC Therapeutics, Inc., South Plainfield, NJ 07080, USA

3. Children's Hospital Colorado, Aurora, CO 80045, USA

Abstract

Aim: To describe reasons for switching from prednisone/prednisolone to deflazacort and associated clinical outcomes among patients with Duchenne and Becker muscular dystrophy (DMD and BMD, respectively) in the USA. Methods: A chart review of patients with DMD (n = 62) or BMD (n = 30) who switched from prednisone to deflazacort (02/2017–12/2018) collected demographic/clinical characteristics, reasons for switching, outcomes and common adverse events. Results: The mean ages at switch were 20.1 (DMD) and 9.2 (BMD) years. The primary physician-reported reasons for switching were ‘to slow disease progression’ (DMD: 83%, BMD: 79%) and ‘tolerability’ (67 and 47%). Switching was ‘very’ or ‘somewhat’ effective at addressing the primary reasons in 90–95% of patients. Conclusion: Physician-reported outcomes were consistent with deflazacort addressing patients' primary reasons for switching.

Funder

PTC Therapeutics

Publisher

Future Medicine Ltd

Subject

Health Policy

Reference24 articles.

1. Dystrophin: The protein product of the duchenne muscular dystrophy locus

2. National Institute of Health (Genetic and Rare Disease Information Center). Becker muscular dystrophy. https://rarediseases.info.nih.gov/diseases/5900/becker-muscular-dystrophy

3. Prevalence of Duchenne and Becker Muscular Dystrophies in the United States

4. Duchenne Muscular Dystrophy

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