Takayasu's arteritis(TAK) is a rare systemic vasculitis which can cause ischemia or inflammation of the involved organs and increase the overall mortality rate.The traditional treatment of TAK is primarily empirical. The most commonly used drugs for treating active TAK are glucocorticosteroids(GC) and immunosuppressants. However, the genital toxicity of CYC has limited its long term use. In a pilot study carried out by the principal investigator of this study has shown that mycophenolate mofetil(MMF) combined with MTX is effective and with few adverse effects. The purpose of this prospective open-label study is to compare the efficacy and safety of GC+MMF+MTX with GC+CYC followed by GC+AZA for the treatment of active TAK. 150 patients with active TAK will be recruited and randomized in a 2:1 ratio to GC+MMF+MTX group and C+CYC and AZA group. Patients were followed for 52 weeks for efficacy and safety assessment.
Takayasu's arteritis(TAK) is a rare systemic vasculitis which mainly involves aorta and its major branches. However,it is more prevalent in countries and areas along the silk road.Young women at child-bearing age is the most prevalent population.It can cause ischemia or inflammation of the involved organs and increase the overall mortality rate.Although it may be lethal in some patients,it is not well studied due to the rareness of the disease.The traditional treatment of TAK is primarily empirical. The most commonly used drugs for treating active TAK are glucocorticosteroids(GC) and immunosuppressants including cyclophosphamide(CYC), methotrexate(MTX) and azathioprine(AZA) etc. However,no of these drugs have been well studied. In addition, the genital toxicity of CYC, the first line medication for active TAK, has become the major limitation for its long term use for a chronic disease like TAK. Therefore, new immunosuppressants with less toxicity,especially with much less genital toxicity and low malignancy risk is essentially necessary. In a pilot study carried out by the principal investigator of this study has shown that mycophenolate mofetil(MMF) combined with MTX is effective and with few adverse effects. The purpose of this prospective open-label study is to compare the efficacy and safety of GC+MMF+MTX with GC+CYC followed by GC+AZA for the treatment of active TAK. 150 patients with active TAK will be recruited and randomized in a 2:1 ratio to GC+MMF+MTX group and C+CYC and AZA group. Patients were followed for 52 weeks to assess the efficacy and safety.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
138
Patients were treated with Glucocorticoids combined with methotrexate and mycophenolate mofetil
Patients were treated with Glucocorticoids and cyclophosphamide sequentially with azathioprine
Patients in the experimental group and comparator group were treated with Glucocorticoids and then gradually tapered
Patients in the experimental group are treated with Glucocorticoids combined with MTX and MMF
Patients in the active comparator group were treated with Glucocorticoids combined with CYC followed by AZA
Hebei Provincial Hospital
Shijiazhuang, Hebei, China
the Affiliated Hospital of Inner Mongolia Medical University
Hohhot, Inner Mongolia, China
Xijing Hospital
Xian, Shanxi, China
Beijing Chaoyang Hospital
Beijing, China
Peking Union Medical College Hospital
Beijing, China
Beijing Xuanwu Hospital
Beijing, China
General Hospital of Tianjing Medical University
Tianjin, China
Proportion of patients with complete remission
The proportion of patients who reached the pre-defined criteria of complete remission in both groups
Time frame: 52 weeks
Proportion of patients with partial remission
Proportion of patients who reached the pre-defined partial remission criteria of the disease
Time frame: 52 weeks
Safety profile of MMF combined with MTX
Proportion of adverse events in both treatment groups
Time frame: 52 weeks
Rate of complications
Proportion of patients with complications in both treatment group
Time frame: 52 weeks
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