Hospital Universitari Germans Trias i Pujol, Badalona, Spain.
J Crohns Colitis. 2011 Oct;5(5):397-401. doi: 10.1016/j.crohns.2011.03.012. Epub 2011 Apr 22.
Few data are available on the efficacy of methotrexate (MTX) in ulcerative colitis (UC).
To evaluate the efficacy and safety of MTX in UC patients.
UC patients who had been treated with MTX were identified from the databases of 8 Spanish IBD referral hospitals. Patients were included in the study if they received MTX for steroid dependency or steroid refractoriness. Therapeutic success was defined as the absence of UC-related symptoms, complete steroid withdrawal and no requirement of rescue therapies within the first 6 months after starting MTX.
Forty patients were included, 70% treated for steroid dependency and 27% for steroid refractoriness. Thiopurines had been previously attempted in 87.5% of patients. The median dose of MTX used for induction was 25mg (IIQ 17.5-25) weekly given parenterally in 82.5% of cases. Eighty-five percent of patients were on steroids when MTX was started. Forty-five percent of patients met criteria for therapeutic success. Initial treatment failures were mainly due to inefficacy (50%) or intolerance (36%). After a median follow-up of 28 months (IQR 22-47), 38% of patients with initial therapeutic success required new steroid courses, 22% started biological therapy, and only 1 patient required colectomy. The cumulative probability of maintaining steroid-free clinical remission was 60%, 48%, and 35% at 6, 12, and 24 months after starting MTX, respectively. Eleven patients (27.5%) experienced adverse events, leading to MTX discontinuation in only 8 of them.
MTX appears to be effective to maintain clinical remission in UC, at least in the short-term, with an acceptable safety profile.
关于甲氨蝶呤(MTX)在溃疡性结肠炎(UC)中的疗效数据较少。
评估 MTX 在 UC 患者中的疗效和安全性。
从 8 家西班牙 IBD 转诊医院的数据库中确定接受 MTX 治疗的 UC 患者。如果患者因类固醇依赖或类固醇抵抗而接受 MTX 治疗,则将其纳入研究。治疗成功定义为 UC 相关症状消失、完全停用类固醇且在开始 MTX 后的前 6 个月内无需进行抢救治疗。
共纳入 40 例患者,70%为类固醇依赖治疗,27%为类固醇抵抗治疗。87.5%的患者之前曾尝试使用硫嘌呤类药物。诱导治疗中 MTX 的中位剂量为 25mg(IIQ 17.5-25),每周静脉给药,占 82.5%。82.5%的患者在开始 MTX 时正在使用类固醇。45%的患者符合治疗成功标准。初始治疗失败主要是由于无效(50%)或不耐受(36%)。中位随访 28 个月(IQR 22-47)后,初始治疗成功的 38%患者需要新的类固醇疗程,22%开始生物治疗,仅有 1 例患者需要结肠切除术。开始 MTX 后 6、12 和 24 个月时,无类固醇临床缓解的累积概率分别为 60%、48%和 35%。11 名患者(27.5%)出现不良反应,仅 8 名患者因此停止 MTX 治疗。
MTX 似乎可有效维持 UC 的临床缓解,至少在短期内如此,且具有可接受的安全性。