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 ¼ 34), CT angiography (n ¼ 5) or magnetic resonance angiography (n ¼ 2). After 2 years, 31 patients remained on MYC, whereas 6 had switched to MTX or tocilizumab owing to significant disease relapse. The mean (6SD) cumulative prednisolone dose at 1 year was 4960 (61621) 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 sub-population. A future randomized controlled trial is warranted.

Evaluation of adjunctive mycophenolate for large vessel giant cell arteritis / Karabayas, M.; Dospinescu, P.; Fluck, N.; Kidder, D.; Fordyce, G.; Hollick, R. J.; De Bari, C.; Basu, N.. - In: RHEUMATOLOGY ADVANCES IN PRACTICE. - ISSN 2514-1775. - 4:2(2020), pp. 1-4. [10.1093/rap/rkaa069]

Evaluation of adjunctive mycophenolate for large vessel giant cell arteritis

de Bari C.;
2020

Abstract

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 ¼ 34), CT angiography (n ¼ 5) or magnetic resonance angiography (n ¼ 2). After 2 years, 31 patients remained on MYC, whereas 6 had switched to MTX or tocilizumab owing to significant disease relapse. The mean (6SD) cumulative prednisolone dose at 1 year was 4960 (61621) 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 sub-population. A future randomized controlled trial is warranted.
2020
4
2
1
4
Evaluation of adjunctive mycophenolate for large vessel giant cell arteritis / Karabayas, M.; Dospinescu, P.; Fluck, N.; Kidder, D.; Fordyce, G.; Hollick, R. J.; De Bari, C.; Basu, N.. - In: RHEUMATOLOGY ADVANCES IN PRACTICE. - ISSN 2514-1775. - 4:2(2020), pp. 1-4. [10.1093/rap/rkaa069]
Karabayas, M.; Dospinescu, P.; Fluck, N.; Kidder, D.; Fordyce, G.; Hollick, R. J.; De Bari, C.; Basu, N.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1381652
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