Cargando…

Long term treatment with ataluren—the Swedish experience

INTRODUCTION: Ataluren is a relatively new treatment for male patients with Duchenne muscular dystrophy (DMD) due to a premature stop codon. Long-term longitudinal data as well as efficacy data on non-ambulant patients are still lacking. Here we present the results from a long-term follow-up study o...

Descripción completa

Detalles Bibliográficos
Autores principales: Michael, Eva, Sofou, Kalliopi, Wahlgren, Lisa, Kroksmark, Anna-Karin, Tulinius, Már
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8485550/
https://www.ncbi.nlm.nih.gov/pubmed/34592975
http://dx.doi.org/10.1186/s12891-021-04700-z
_version_ 1784577558204907520
author Michael, Eva
Sofou, Kalliopi
Wahlgren, Lisa
Kroksmark, Anna-Karin
Tulinius, Már
author_facet Michael, Eva
Sofou, Kalliopi
Wahlgren, Lisa
Kroksmark, Anna-Karin
Tulinius, Már
author_sort Michael, Eva
collection PubMed
description INTRODUCTION: Ataluren is a relatively new treatment for male patients with Duchenne muscular dystrophy (DMD) due to a premature stop codon. Long-term longitudinal data as well as efficacy data on non-ambulant patients are still lacking. Here we present the results from a long-term follow-up study of all DMD patients treated with ataluren and followed at the Queen Silvia Children’s Hospital in Gothenburg, Sweden, with focus on the evolution of patients’ upper motor and respiratory function over time. METHODS: This is a retrospective longitudinal case-series study of all male DMD patients treated with ataluren and followed at the Queen Silvia Children’s Hospital in Gothenburg, Sweden, since 2008. RESULTS: Our eleven patients had a median exposure to ataluren of 2312 days which is almost a fourfold higher than previous studies. Loss of ambulation occurred at a median age of 13.2 years. Patients who lost ambulation prior to 13.2 years of age had received ataluren for 5 years, whereas patients who continued to be ambulatory after 13.2 years of age had received ataluren for 6.5 years until loss of ambulation or last follow-up if still ambulatory. Four of six non ambulatory patients had Performance of the Upper Limb scores above the expected mean values over time. All but one patient maintained a pulmonary decline above the expected over time. All ambulatory patients increased in their predicted forced vital capacity (FVC) with 2.8 to 8.2% annually. Following loss of ambulation, 5 of 6 patients declined in predicted FVC (%), with annual rate of decline varying from 1.8 to 21.1%. The treatment was safe and well tolerated throughout the follow-up period. CONCLUSIONS: This is the first study to present long-term cumulative treatment outcomes over a median period of 6.3 years on ataluren treatment. Our results indicate a delay in loss of ambulation, as well as a slower decline in FVC and upper limb motor function even after loss of ambulation. We suggest that treatment with ataluren should be initiated as soon as the diagnosis is confirmed, closely monitored and, in case of sustainable benefit, continued even after loss of ambulation.
format Online
Article
Text
id pubmed-8485550
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-84855502021-10-04 Long term treatment with ataluren—the Swedish experience Michael, Eva Sofou, Kalliopi Wahlgren, Lisa Kroksmark, Anna-Karin Tulinius, Már BMC Musculoskelet Disord Research INTRODUCTION: Ataluren is a relatively new treatment for male patients with Duchenne muscular dystrophy (DMD) due to a premature stop codon. Long-term longitudinal data as well as efficacy data on non-ambulant patients are still lacking. Here we present the results from a long-term follow-up study of all DMD patients treated with ataluren and followed at the Queen Silvia Children’s Hospital in Gothenburg, Sweden, with focus on the evolution of patients’ upper motor and respiratory function over time. METHODS: This is a retrospective longitudinal case-series study of all male DMD patients treated with ataluren and followed at the Queen Silvia Children’s Hospital in Gothenburg, Sweden, since 2008. RESULTS: Our eleven patients had a median exposure to ataluren of 2312 days which is almost a fourfold higher than previous studies. Loss of ambulation occurred at a median age of 13.2 years. Patients who lost ambulation prior to 13.2 years of age had received ataluren for 5 years, whereas patients who continued to be ambulatory after 13.2 years of age had received ataluren for 6.5 years until loss of ambulation or last follow-up if still ambulatory. Four of six non ambulatory patients had Performance of the Upper Limb scores above the expected mean values over time. All but one patient maintained a pulmonary decline above the expected over time. All ambulatory patients increased in their predicted forced vital capacity (FVC) with 2.8 to 8.2% annually. Following loss of ambulation, 5 of 6 patients declined in predicted FVC (%), with annual rate of decline varying from 1.8 to 21.1%. The treatment was safe and well tolerated throughout the follow-up period. CONCLUSIONS: This is the first study to present long-term cumulative treatment outcomes over a median period of 6.3 years on ataluren treatment. Our results indicate a delay in loss of ambulation, as well as a slower decline in FVC and upper limb motor function even after loss of ambulation. We suggest that treatment with ataluren should be initiated as soon as the diagnosis is confirmed, closely monitored and, in case of sustainable benefit, continued even after loss of ambulation. BioMed Central 2021-09-30 /pmc/articles/PMC8485550/ /pubmed/34592975 http://dx.doi.org/10.1186/s12891-021-04700-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Michael, Eva
Sofou, Kalliopi
Wahlgren, Lisa
Kroksmark, Anna-Karin
Tulinius, Már
Long term treatment with ataluren—the Swedish experience
title Long term treatment with ataluren—the Swedish experience
title_full Long term treatment with ataluren—the Swedish experience
title_fullStr Long term treatment with ataluren—the Swedish experience
title_full_unstemmed Long term treatment with ataluren—the Swedish experience
title_short Long term treatment with ataluren—the Swedish experience
title_sort long term treatment with ataluren—the swedish experience
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8485550/
https://www.ncbi.nlm.nih.gov/pubmed/34592975
http://dx.doi.org/10.1186/s12891-021-04700-z
work_keys_str_mv AT michaeleva longtermtreatmentwithatalurentheswedishexperience
AT sofoukalliopi longtermtreatmentwithatalurentheswedishexperience
AT wahlgrenlisa longtermtreatmentwithatalurentheswedishexperience
AT kroksmarkannakarin longtermtreatmentwithatalurentheswedishexperience
AT tuliniusmar longtermtreatmentwithatalurentheswedishexperience