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Disease activity 4.5 years after starting cladribine: experience in 264 patients with multiple sclerosis
BACKGROUND: Cladribine is an effective immunotherapy for people with multiple sclerosis (pwMS). Whilst most pwMS do not require re-treatment following standard dosing (two treatment courses), disease activity re-emerges in others. The characteristics of pwMS developing re-emerging disease activity r...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10638874/ https://www.ncbi.nlm.nih.gov/pubmed/37954917 http://dx.doi.org/10.1177/17562864231200627 |
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author | Allen-Philbey, Kimberley De Trane, Stefania MacDougall, Amy Adams, Ashok Bianchi, Lucia Campion, Thomas Giovannoni, Gavin Gnanapavan, Sharmilee Holden, David W. Marta, Monica Mathews, Joela Turner, Benjamin P. Baker, David Schmierer, Klaus |
author_facet | Allen-Philbey, Kimberley De Trane, Stefania MacDougall, Amy Adams, Ashok Bianchi, Lucia Campion, Thomas Giovannoni, Gavin Gnanapavan, Sharmilee Holden, David W. Marta, Monica Mathews, Joela Turner, Benjamin P. Baker, David Schmierer, Klaus |
author_sort | Allen-Philbey, Kimberley |
collection | PubMed |
description | BACKGROUND: Cladribine is an effective immunotherapy for people with multiple sclerosis (pwMS). Whilst most pwMS do not require re-treatment following standard dosing (two treatment courses), disease activity re-emerges in others. The characteristics of pwMS developing re-emerging disease activity remain incompletely understood. OBJECTIVES: To explore whether clinical and/or paraclinical baseline characteristics, including the degree of lymphocyte reduction, drug dose and lesions on magnetic resonance imaging (MRI) are associated with re-emerging disease activity. DESIGN: Service evaluation in pwMS undergoing subcutaneous cladribine (SClad) treatment. METHODS: Demographics, clinical, laboratory and MRI data of pwMS receiving two courses of SClad were extracted from health records. To assess associations of predictor variables with re-emerging disease activity, a series of Cox proportional hazards models was fitted (one for each predictor variable). RESULTS: Of n = 264 pwMS 236 received two courses of SClad and were included in the analysis. Median follow-up was 4.5 years (3.9, 5.3) from the first, and 3.5 years (2.9, 4.3) from the last SClad administration. Re-emerging disease activity occurred in 57/236 pwMS (24%); 22/236 received further cladribine doses (SClad or cladribine tablets) at 36.7 months [median; interquartile range (IQR): 31.7, 42.1], and 22/236 other immunotherapies 18.9 months (13.0, 30.2) after their second course of SClad, respectively. Eligibility was based on MRI activity in 29, relapse in 5, both in 13, elevated cerebrospinal fluid neurofilament light chain level in 3, deterioration unrelated to relapse in 4 and other in 3. Only 36/57 of those eligible for additional immunotherapy had received a reduced dose of SClad for their second treatment course. Association was detected between re-emerging disease activity and (i) high baseline MRI activity and (ii) low second dose of SClad. CONCLUSION: Re-emerging disease activity was associated with baseline MRI activity and low dose second course of SClad. |
format | Online Article Text |
id | pubmed-10638874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-106388742023-11-11 Disease activity 4.5 years after starting cladribine: experience in 264 patients with multiple sclerosis Allen-Philbey, Kimberley De Trane, Stefania MacDougall, Amy Adams, Ashok Bianchi, Lucia Campion, Thomas Giovannoni, Gavin Gnanapavan, Sharmilee Holden, David W. Marta, Monica Mathews, Joela Turner, Benjamin P. Baker, David Schmierer, Klaus Ther Adv Neurol Disord Original Research BACKGROUND: Cladribine is an effective immunotherapy for people with multiple sclerosis (pwMS). Whilst most pwMS do not require re-treatment following standard dosing (two treatment courses), disease activity re-emerges in others. The characteristics of pwMS developing re-emerging disease activity remain incompletely understood. OBJECTIVES: To explore whether clinical and/or paraclinical baseline characteristics, including the degree of lymphocyte reduction, drug dose and lesions on magnetic resonance imaging (MRI) are associated with re-emerging disease activity. DESIGN: Service evaluation in pwMS undergoing subcutaneous cladribine (SClad) treatment. METHODS: Demographics, clinical, laboratory and MRI data of pwMS receiving two courses of SClad were extracted from health records. To assess associations of predictor variables with re-emerging disease activity, a series of Cox proportional hazards models was fitted (one for each predictor variable). RESULTS: Of n = 264 pwMS 236 received two courses of SClad and were included in the analysis. Median follow-up was 4.5 years (3.9, 5.3) from the first, and 3.5 years (2.9, 4.3) from the last SClad administration. Re-emerging disease activity occurred in 57/236 pwMS (24%); 22/236 received further cladribine doses (SClad or cladribine tablets) at 36.7 months [median; interquartile range (IQR): 31.7, 42.1], and 22/236 other immunotherapies 18.9 months (13.0, 30.2) after their second course of SClad, respectively. Eligibility was based on MRI activity in 29, relapse in 5, both in 13, elevated cerebrospinal fluid neurofilament light chain level in 3, deterioration unrelated to relapse in 4 and other in 3. Only 36/57 of those eligible for additional immunotherapy had received a reduced dose of SClad for their second treatment course. Association was detected between re-emerging disease activity and (i) high baseline MRI activity and (ii) low second dose of SClad. CONCLUSION: Re-emerging disease activity was associated with baseline MRI activity and low dose second course of SClad. SAGE Publications 2023-11-10 /pmc/articles/PMC10638874/ /pubmed/37954917 http://dx.doi.org/10.1177/17562864231200627 Text en © The Author(s), 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Allen-Philbey, Kimberley De Trane, Stefania MacDougall, Amy Adams, Ashok Bianchi, Lucia Campion, Thomas Giovannoni, Gavin Gnanapavan, Sharmilee Holden, David W. Marta, Monica Mathews, Joela Turner, Benjamin P. Baker, David Schmierer, Klaus Disease activity 4.5 years after starting cladribine: experience in 264 patients with multiple sclerosis |
title | Disease activity 4.5 years after starting cladribine: experience in 264 patients with multiple sclerosis |
title_full | Disease activity 4.5 years after starting cladribine: experience in 264 patients with multiple sclerosis |
title_fullStr | Disease activity 4.5 years after starting cladribine: experience in 264 patients with multiple sclerosis |
title_full_unstemmed | Disease activity 4.5 years after starting cladribine: experience in 264 patients with multiple sclerosis |
title_short | Disease activity 4.5 years after starting cladribine: experience in 264 patients with multiple sclerosis |
title_sort | disease activity 4.5 years after starting cladribine: experience in 264 patients with multiple sclerosis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10638874/ https://www.ncbi.nlm.nih.gov/pubmed/37954917 http://dx.doi.org/10.1177/17562864231200627 |
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