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Effectiveness and safety of methotrexate leflunomide in 12-month treatment for Takayasu arteritis

Authors :
Chunling Wu
Ying Sun
Xiaomeng Cui
Sifan Wu
Lili Ma
Huiyong Chen
Yan Yan
Zongfei Ji
Yun Liu
Jiang Lin
Peng Lv
Rongyi Chen
Pingting Yang
Lindi Jiang
Source :
Therapeutic Advances in Chronic Disease, Vol 11 (2020)
Publication Year :
2020
Publisher :
SAGE Publishing, 2020.

Abstract

Aims: The study investigates the effectiveness and safety of methotrexate (MTX) versus leflunomide (LEF) in 12-month treatment of Takayasu arteritis (TAK). Methods: This was a cohort study. Patients diagnosed with TAK between 1 January 2013 and 1 January 2019 were enrolled from First Hospital of China Medical University and Zhongshan Hospital of Fudan University. Patients had active disease and were treated with glucocorticoid combined with LEF or MTX. Treatment response, imaging assessment and side-effects were evaluated during 12-month follow-up. Results: In total, 68 patients were enrolled (40 cases treated with LEF and 28 treated with MTX). At baseline, age, sex, disease duration and disease activity index showed no significant differences between groups. Prevalence of complete remission (CR) at 6 months was significantly higher in the LEF group than that in the MTX group (LEF versus MTX: 72.50% versus 53.57%, p = 0.04), though the CR prevalence at 9 months and 12 months showed no significant differences between groups. At 9 months, the prevalence of treatment resistance was much lower in the LEF group compared with MTX group (5.41% versus 11.54%, p = 0.03). Furthermore, prevalence of disease relapse in the LEF group was lower than that in MTX group at 12 months (7.24% versus 16.67%, p = 0.03). Patients with high baseline C-reactive protein levels (⩾15 mg/L) carried a higher risk of treatment resistance (OR = 1.36, 95% CI 1.07–13.41, p = 0.06) and disease relapse (HR = 2.51, 95% CI 1.36–12.98, p = 0.04). Conclusion: LEF might provide a quicker treatment response with lower prevalence of disease relapse compared with that elicited in MTX during 12 months follow-up for TAK.

Subjects

Subjects :
Therapeutics. Pharmacology
RM1-950

Details

Language :
English
ISSN :
20406231 and 20406223
Volume :
11
Database :
Directory of Open Access Journals
Journal :
Therapeutic Advances in Chronic Disease
Publication Type :
Academic Journal
Accession number :
edsdoj.234dead1a0db43fdb94f530e41a0ffee
Document Type :
article
Full Text :
https://doi.org/10.1177/2040622320975233