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Evaluation of adjunctive mycophenolate for large vessel giant cell arteritis

OBJECTIVES: GCA patients with large vessel involvement (LV-GCA) experience greater CS requirements and higher relapse rates compared with classical cranial GCA. Despite the distinct disease course, interventions in LV-GCA have yet to be investigated specifically. This study aimed to evaluate the CS-...

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Autores principales: Karabayas, Maira, Dospinescu, Paula, Fluck, Nick, Kidder, Dana, Fordyce, Gillian, Hollick, Rosemary J, De Bari, Cosimo, Basu, Neil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756006/
https://www.ncbi.nlm.nih.gov/pubmed/33381680
http://dx.doi.org/10.1093/rap/rkaa069
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author Karabayas, Maira
Dospinescu, Paula
Fluck, Nick
Kidder, Dana
Fordyce, Gillian
Hollick, Rosemary J
De Bari, Cosimo
Basu, Neil
author_facet Karabayas, Maira
Dospinescu, Paula
Fluck, Nick
Kidder, Dana
Fordyce, Gillian
Hollick, Rosemary J
De Bari, Cosimo
Basu, Neil
author_sort Karabayas, Maira
collection PubMed
description OBJECTIVES: GCA patients with large vessel involvement (LV-GCA) experience greater CS requirements and higher relapse rates compared with classical cranial GCA. Despite the distinct disease course, interventions in LV-GCA have yet to be investigated specifically. This study aimed to evaluate the CS-sparing effect and tolerability of first-line mycophenolate in LV-GCA. METHODS: A retrospective cohort study was conducted in patients with LV-GCA identified from a regional clinical database between 2005 and 2019. All cases were prescribed mycophenolate derivatives (MYC; MMF or mycophenolic acid) at diagnosis and were followed up for ≥2 years. The primary outcome was the cumulative CS dose at 1 year. Secondary outcomes included MYC tolerance, relapse rates and CRP levels at 1 and 2 years. RESULTS: A total of 37 patients (65% female; mean age 69.4 years, SD 7.9 years) were identified. All cases demonstrated large vessel involvement via CT/PET (n = 34), CT angiography (n = 5) or magnetic resonance angiography (n = 2). After 2 years, 31 patients remained on MYC, whereas 6 had switched to MTX or tocilizumab owing to significant disease relapse. The mean (±SD) cumulative prednisolone dose at 1 year was 4960 (±1621) mg. Relapse rates at 1 and 2 years were 16.2 and 27%, respectively, and CRP levels at 1 and 2 years were 4 [interquartile range (IQR) 4–6] and 4 (IQR 4–4) mg/l, respectively. CONCLUSION: To our knowledge, this is the first attempt to assess the effectiveness of any specific agent in LV-GCA. MYC might be both effective in reducing CS exposure and well tolerated in this subpopulation. A future randomized controlled trial is warranted.
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spelling pubmed-77560062020-12-29 Evaluation of adjunctive mycophenolate for large vessel giant cell arteritis Karabayas, Maira Dospinescu, Paula Fluck, Nick Kidder, Dana Fordyce, Gillian Hollick, Rosemary J De Bari, Cosimo Basu, Neil Rheumatol Adv Pract Concise Report OBJECTIVES: GCA patients with large vessel involvement (LV-GCA) experience greater CS requirements and higher relapse rates compared with classical cranial GCA. Despite the distinct disease course, interventions in LV-GCA have yet to be investigated specifically. This study aimed to evaluate the CS-sparing effect and tolerability of first-line mycophenolate in LV-GCA. METHODS: A retrospective cohort study was conducted in patients with LV-GCA identified from a regional clinical database between 2005 and 2019. All cases were prescribed mycophenolate derivatives (MYC; MMF or mycophenolic acid) at diagnosis and were followed up for ≥2 years. The primary outcome was the cumulative CS dose at 1 year. Secondary outcomes included MYC tolerance, relapse rates and CRP levels at 1 and 2 years. RESULTS: A total of 37 patients (65% female; mean age 69.4 years, SD 7.9 years) were identified. All cases demonstrated large vessel involvement via CT/PET (n = 34), CT angiography (n = 5) or magnetic resonance angiography (n = 2). After 2 years, 31 patients remained on MYC, whereas 6 had switched to MTX or tocilizumab owing to significant disease relapse. The mean (±SD) cumulative prednisolone dose at 1 year was 4960 (±1621) mg. Relapse rates at 1 and 2 years were 16.2 and 27%, respectively, and CRP levels at 1 and 2 years were 4 [interquartile range (IQR) 4–6] and 4 (IQR 4–4) mg/l, respectively. CONCLUSION: To our knowledge, this is the first attempt to assess the effectiveness of any specific agent in LV-GCA. MYC might be both effective in reducing CS exposure and well tolerated in this subpopulation. A future randomized controlled trial is warranted. Oxford University Press 2020-12-19 /pmc/articles/PMC7756006/ /pubmed/33381680 http://dx.doi.org/10.1093/rap/rkaa069 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Rheumatology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Concise Report
Karabayas, Maira
Dospinescu, Paula
Fluck, Nick
Kidder, Dana
Fordyce, Gillian
Hollick, Rosemary J
De Bari, Cosimo
Basu, Neil
Evaluation of adjunctive mycophenolate for large vessel giant cell arteritis
title Evaluation of adjunctive mycophenolate for large vessel giant cell arteritis
title_full Evaluation of adjunctive mycophenolate for large vessel giant cell arteritis
title_fullStr Evaluation of adjunctive mycophenolate for large vessel giant cell arteritis
title_full_unstemmed Evaluation of adjunctive mycophenolate for large vessel giant cell arteritis
title_short Evaluation of adjunctive mycophenolate for large vessel giant cell arteritis
title_sort evaluation of adjunctive mycophenolate for large vessel giant cell arteritis
topic Concise Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756006/
https://www.ncbi.nlm.nih.gov/pubmed/33381680
http://dx.doi.org/10.1093/rap/rkaa069
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