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Lithium carbonate in amyotrophic lateral sclerosis patients homozygous for the C-allele at SNP rs12608932 in UNC13A: protocol for a confirmatory, randomized, group-sequential, event-driven, double-blind, placebo-controlled trial
BACKGROUND: Given the large genetic heterogeneity in amyotrophic lateral sclerosis (ALS), it seems likely that genetic subgroups may benefit differently from treatment. An exploratory meta-analysis identified that patients homozygous for the C-allele at SNP rs12608932, a single nucleotide polymorphi...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9721045/ https://www.ncbi.nlm.nih.gov/pubmed/36471413 http://dx.doi.org/10.1186/s13063-022-06906-5 |
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author | Willemse, Sean W. Roes, Kit C. B. Van Damme, Philip Hardiman, Orla Ingre, Caroline Povedano, Monica Wray, Naomi R. Gijzen, Marleen de Pagter, Mirjam S. Demaegd, Koen C. Janse, Annemarie F. C. Vink, Roel G. Sleutjes, Boudewijn T. H. M. Chiò, Adriano Corcia, Philippe Reviers, Evy Al-Chalabi, Ammar Kiernan, Matthew C. van den Berg, Leonard H. van Es, Michael A. van Eijk, Ruben P. A. |
author_facet | Willemse, Sean W. Roes, Kit C. B. Van Damme, Philip Hardiman, Orla Ingre, Caroline Povedano, Monica Wray, Naomi R. Gijzen, Marleen de Pagter, Mirjam S. Demaegd, Koen C. Janse, Annemarie F. C. Vink, Roel G. Sleutjes, Boudewijn T. H. M. Chiò, Adriano Corcia, Philippe Reviers, Evy Al-Chalabi, Ammar Kiernan, Matthew C. van den Berg, Leonard H. van Es, Michael A. van Eijk, Ruben P. A. |
author_sort | Willemse, Sean W. |
collection | PubMed |
description | BACKGROUND: Given the large genetic heterogeneity in amyotrophic lateral sclerosis (ALS), it seems likely that genetic subgroups may benefit differently from treatment. An exploratory meta-analysis identified that patients homozygous for the C-allele at SNP rs12608932, a single nucleotide polymorphism in the gene UNC13A, had a statistically significant survival benefit when treated with lithium carbonate. We aim to confirm the efficacy of lithium carbonate on the time to death or respiratory insufficiency in patients with ALS homozygous for the C-allele at SNP rs12608932 in UNC13A. METHODS: A randomized, group-sequential, event-driven, double-blind, placebo-controlled trial will be conducted in 15 sites across Europe and Australia. Patients will be genotyped for UNC13A; those homozygous for the C-allele at SNP rs12608932 will be eligible. Patients must have a diagnosis of ALS according to the revised El Escorial criteria, and a TRICALS risk-profile score between −6.0 and −2.0. An expected number of 1200 patients will be screened in order to enroll a target sample size of 171 patients. Patients will be randomly allocated in a 2:1 ratio to lithium carbonate or matching placebo, and treated for a maximum duration of 24 months. The primary endpoint is the time to death or respiratory insufficiency, whichever occurs first. Key secondary endpoints include functional decline, respiratory function, quality of life, tolerability, and safety. An interim analysis for futility and efficacy will be conducted after the occurrence of 41 events. DISCUSSION: Lithium carbonate has been proven to be safe and well-tolerated in patients with ALS. Given the favorable safety profile, the potential benefits are considered to outweigh the burden and risks associated with study participation. This study may provide conclusive evidence about the life-prolonging potential of lithium carbonate in a genetic ALS subgroup. TRIAL REGISTRATION: EudraCT number 2020-000579-19. Registered on 29 March 2021. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13063-022-06906-5. |
format | Online Article Text |
id | pubmed-9721045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97210452022-12-06 Lithium carbonate in amyotrophic lateral sclerosis patients homozygous for the C-allele at SNP rs12608932 in UNC13A: protocol for a confirmatory, randomized, group-sequential, event-driven, double-blind, placebo-controlled trial Willemse, Sean W. Roes, Kit C. B. Van Damme, Philip Hardiman, Orla Ingre, Caroline Povedano, Monica Wray, Naomi R. Gijzen, Marleen de Pagter, Mirjam S. Demaegd, Koen C. Janse, Annemarie F. C. Vink, Roel G. Sleutjes, Boudewijn T. H. M. Chiò, Adriano Corcia, Philippe Reviers, Evy Al-Chalabi, Ammar Kiernan, Matthew C. van den Berg, Leonard H. van Es, Michael A. van Eijk, Ruben P. A. Trials Study Protocol BACKGROUND: Given the large genetic heterogeneity in amyotrophic lateral sclerosis (ALS), it seems likely that genetic subgroups may benefit differently from treatment. An exploratory meta-analysis identified that patients homozygous for the C-allele at SNP rs12608932, a single nucleotide polymorphism in the gene UNC13A, had a statistically significant survival benefit when treated with lithium carbonate. We aim to confirm the efficacy of lithium carbonate on the time to death or respiratory insufficiency in patients with ALS homozygous for the C-allele at SNP rs12608932 in UNC13A. METHODS: A randomized, group-sequential, event-driven, double-blind, placebo-controlled trial will be conducted in 15 sites across Europe and Australia. Patients will be genotyped for UNC13A; those homozygous for the C-allele at SNP rs12608932 will be eligible. Patients must have a diagnosis of ALS according to the revised El Escorial criteria, and a TRICALS risk-profile score between −6.0 and −2.0. An expected number of 1200 patients will be screened in order to enroll a target sample size of 171 patients. Patients will be randomly allocated in a 2:1 ratio to lithium carbonate or matching placebo, and treated for a maximum duration of 24 months. The primary endpoint is the time to death or respiratory insufficiency, whichever occurs first. Key secondary endpoints include functional decline, respiratory function, quality of life, tolerability, and safety. An interim analysis for futility and efficacy will be conducted after the occurrence of 41 events. DISCUSSION: Lithium carbonate has been proven to be safe and well-tolerated in patients with ALS. Given the favorable safety profile, the potential benefits are considered to outweigh the burden and risks associated with study participation. This study may provide conclusive evidence about the life-prolonging potential of lithium carbonate in a genetic ALS subgroup. TRIAL REGISTRATION: EudraCT number 2020-000579-19. Registered on 29 March 2021. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13063-022-06906-5. BioMed Central 2022-12-05 /pmc/articles/PMC9721045/ /pubmed/36471413 http://dx.doi.org/10.1186/s13063-022-06906-5 Text en © The Author(s) 2022 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 | Study Protocol Willemse, Sean W. Roes, Kit C. B. Van Damme, Philip Hardiman, Orla Ingre, Caroline Povedano, Monica Wray, Naomi R. Gijzen, Marleen de Pagter, Mirjam S. Demaegd, Koen C. Janse, Annemarie F. C. Vink, Roel G. Sleutjes, Boudewijn T. H. M. Chiò, Adriano Corcia, Philippe Reviers, Evy Al-Chalabi, Ammar Kiernan, Matthew C. van den Berg, Leonard H. van Es, Michael A. van Eijk, Ruben P. A. Lithium carbonate in amyotrophic lateral sclerosis patients homozygous for the C-allele at SNP rs12608932 in UNC13A: protocol for a confirmatory, randomized, group-sequential, event-driven, double-blind, placebo-controlled trial |
title | Lithium carbonate in amyotrophic lateral sclerosis patients homozygous for the C-allele at SNP rs12608932 in UNC13A: protocol for a confirmatory, randomized, group-sequential, event-driven, double-blind, placebo-controlled trial |
title_full | Lithium carbonate in amyotrophic lateral sclerosis patients homozygous for the C-allele at SNP rs12608932 in UNC13A: protocol for a confirmatory, randomized, group-sequential, event-driven, double-blind, placebo-controlled trial |
title_fullStr | Lithium carbonate in amyotrophic lateral sclerosis patients homozygous for the C-allele at SNP rs12608932 in UNC13A: protocol for a confirmatory, randomized, group-sequential, event-driven, double-blind, placebo-controlled trial |
title_full_unstemmed | Lithium carbonate in amyotrophic lateral sclerosis patients homozygous for the C-allele at SNP rs12608932 in UNC13A: protocol for a confirmatory, randomized, group-sequential, event-driven, double-blind, placebo-controlled trial |
title_short | Lithium carbonate in amyotrophic lateral sclerosis patients homozygous for the C-allele at SNP rs12608932 in UNC13A: protocol for a confirmatory, randomized, group-sequential, event-driven, double-blind, placebo-controlled trial |
title_sort | lithium carbonate in amyotrophic lateral sclerosis patients homozygous for the c-allele at snp rs12608932 in unc13a: protocol for a confirmatory, randomized, group-sequential, event-driven, double-blind, placebo-controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9721045/ https://www.ncbi.nlm.nih.gov/pubmed/36471413 http://dx.doi.org/10.1186/s13063-022-06906-5 |
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