Department of Gastroenterology, Ankara City Hospital, Ankara, Turkey.
Department of Gastroenterology, TOBB University of Economics and Technology Faculty of Medicine, Ankara, Turkey.
Turk J Gastroenterol. 2022 Feb;33(2):111-118. doi: 10.5152/tjg.2022.21459.
There is limited data in the literature analyzing the efficacy of methotrexate in Crohn's disease used after thiopurine analogs. We aimed in our study to show the efficacy of methotrexate in Crohn's disease patients who failed to respond to thiopurine treatment.
The study included 29 azathioprine refractory patients with Crohn's disease. Intramuscular methotrexate (25 mg/week) in the induction of remission and intramuscular methotrexate (15 mg/week) in 29 CD patients with a median follow-up time of 13 months was performed. In 15 (51.7%) patients, methotrexate was used in combination with anti-Tumour necrosis factor (TNF) (combination group), while it was used in 14 (48.3%) patients in monotherapy (monotherapy group).
The mean Harvey-Bradshaw index score significantly decreased in the follow-up period (Wk0 = 7.6, last visit = 4.5, P < .001). Remission and response rates at week 12 were 75.9% and 79.3%, respectively. Maintenance of remission (77.8% vs 37.5%, respectively, P = .1) and response rates (77.8% vs 50%, respectively, P = .3) due to last visit examination were numerically higher in combination group but they were not statistically significant. The cumulative probability of remission maintenance in patients with methotrexate therapy was 72.7%, 33.1%, and 22.0% at 1, 2 ,and 4 years after starting methotrexate, respectively.
Our results show that parenteral use of methotrexate is efficacious in inducing and maintaining remission as a step-up agent in azathioprine refractory Crohn's disease patients.
在文献中,关于硫嘌呤类似物治疗失败后使用甲氨蝶呤治疗克罗恩病的疗效数据有限。我们的研究旨在显示甲氨蝶呤在对硫嘌呤治疗无反应的克罗恩病患者中的疗效。
该研究纳入了 29 例对硫嘌呤耐药的克罗恩病患者。对 29 例 CD 患者进行了诱导缓解的肌肉内甲氨蝶呤(25mg/周)和 13 个月中位随访时间的肌肉内甲氨蝶呤(15mg/周)。在 15 例(51.7%)患者中,甲氨蝶呤与抗肿瘤坏死因子(TNF)联合使用(联合组),而在 14 例(48.3%)患者中则单独使用(单药组)。
在随访期间,平均 Harvey-Bradshaw 指数评分显著下降(Wk0=7.6,末次就诊=4.5,P<.001)。在第 12 周时,缓解率和应答率分别为 75.9%和 79.3%。在联合组中,缓解(分别为 77.8%和 37.5%,P=0.1)和应答(分别为 77.8%和 50%,P=0.3)的维持率在末次就诊时均高于单药组,但无统计学意义。在接受甲氨蝶呤治疗的患者中,甲氨蝶呤治疗后 1、2、4 年的缓解维持累积概率分别为 72.7%、33.1%和 22.0%。
我们的结果表明,在对硫嘌呤耐药的克罗恩病患者中,作为硫嘌呤耐药的升级治疗药物,静脉用甲氨蝶呤诱导和维持缓解是有效的。