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Durability of no evidence of disease activity-3 (NEDA-3) in patients receiving cladribine tablets: The CLARITY extension study
BACKGROUND: No evidence of disease activity (NEDA-3) is a patient-centric outcome increasingly used as the goal of multiple sclerosis treatment. OBJECTIVE: Determine treatment durability of cladribine tablets beyond 2 years considering the variable bridging interval of 0.1–116.0 weeks between CLARIT...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189728/ https://www.ncbi.nlm.nih.gov/pubmed/34634968 http://dx.doi.org/10.1177/13524585211049392 |
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author | Giovannoni, Gavin Singer, Barry A Issard, Delphine Jack, Dominic Vermersch, Patrick |
author_facet | Giovannoni, Gavin Singer, Barry A Issard, Delphine Jack, Dominic Vermersch, Patrick |
author_sort | Giovannoni, Gavin |
collection | PubMed |
description | BACKGROUND: No evidence of disease activity (NEDA-3) is a patient-centric outcome increasingly used as the goal of multiple sclerosis treatment. OBJECTIVE: Determine treatment durability of cladribine tablets beyond 2 years considering the variable bridging interval of 0.1–116.0 weeks between CLARITY and CLARITY Extension. METHODS: Between CLARITY and CLARITY Extension, patients transitioned from cladribine tablets 3.5 mg/kg to placebo (CP3.5 group, n = 98) or continued further treatment with cladribine tablets 3.5 mg/kg (CC7.0 group, n = 186). Treatment assignment was randomized and blinded in both CLARITY and CLARITY Extension. RESULTS: The 2-year NEDA-3 in CLARITY Extension (encompassing both years of CLARITY Extension) was 29.6% in the CP3.5 group and 32.8% in the CC7.0 group. There was no evidence that treatment effect differed with varying bridging intervals. For patients in the CP3.5 group with a bridging interval of ⩽48 weeks, 1 year NEDA-3 (the first year of CLARITY Extension) was 44.4% (28/63) compared with 31.4% (11/35) in patients with a bridging interval of >48 weeks. CONCLUSION: Treatment with cladribine tablets in CLARITY, followed by either placebo or cladribine tablets in CLARITY Extension, produced sustained benefits for NEDA-3 and its constituent elements for a follow up period up to 6 years from CLARITY baseline. |
format | Online Article Text |
id | pubmed-9189728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-91897282022-06-14 Durability of no evidence of disease activity-3 (NEDA-3) in patients receiving cladribine tablets: The CLARITY extension study Giovannoni, Gavin Singer, Barry A Issard, Delphine Jack, Dominic Vermersch, Patrick Mult Scler Original Research Papers BACKGROUND: No evidence of disease activity (NEDA-3) is a patient-centric outcome increasingly used as the goal of multiple sclerosis treatment. OBJECTIVE: Determine treatment durability of cladribine tablets beyond 2 years considering the variable bridging interval of 0.1–116.0 weeks between CLARITY and CLARITY Extension. METHODS: Between CLARITY and CLARITY Extension, patients transitioned from cladribine tablets 3.5 mg/kg to placebo (CP3.5 group, n = 98) or continued further treatment with cladribine tablets 3.5 mg/kg (CC7.0 group, n = 186). Treatment assignment was randomized and blinded in both CLARITY and CLARITY Extension. RESULTS: The 2-year NEDA-3 in CLARITY Extension (encompassing both years of CLARITY Extension) was 29.6% in the CP3.5 group and 32.8% in the CC7.0 group. There was no evidence that treatment effect differed with varying bridging intervals. For patients in the CP3.5 group with a bridging interval of ⩽48 weeks, 1 year NEDA-3 (the first year of CLARITY Extension) was 44.4% (28/63) compared with 31.4% (11/35) in patients with a bridging interval of >48 weeks. CONCLUSION: Treatment with cladribine tablets in CLARITY, followed by either placebo or cladribine tablets in CLARITY Extension, produced sustained benefits for NEDA-3 and its constituent elements for a follow up period up to 6 years from CLARITY baseline. SAGE Publications 2021-10-12 2022-07 /pmc/articles/PMC9189728/ /pubmed/34634968 http://dx.doi.org/10.1177/13524585211049392 Text en © The Author(s), 2021 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 Papers Giovannoni, Gavin Singer, Barry A Issard, Delphine Jack, Dominic Vermersch, Patrick Durability of no evidence of disease activity-3 (NEDA-3) in patients receiving cladribine tablets: The CLARITY extension study |
title | Durability of no evidence of disease activity-3 (NEDA-3) in patients
receiving cladribine tablets: The CLARITY extension study |
title_full | Durability of no evidence of disease activity-3 (NEDA-3) in patients
receiving cladribine tablets: The CLARITY extension study |
title_fullStr | Durability of no evidence of disease activity-3 (NEDA-3) in patients
receiving cladribine tablets: The CLARITY extension study |
title_full_unstemmed | Durability of no evidence of disease activity-3 (NEDA-3) in patients
receiving cladribine tablets: The CLARITY extension study |
title_short | Durability of no evidence of disease activity-3 (NEDA-3) in patients
receiving cladribine tablets: The CLARITY extension study |
title_sort | durability of no evidence of disease activity-3 (neda-3) in patients
receiving cladribine tablets: the clarity extension study |
topic | Original Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189728/ https://www.ncbi.nlm.nih.gov/pubmed/34634968 http://dx.doi.org/10.1177/13524585211049392 |
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