Department of Medicine, Division of Gastroenterology, Inflammatory Bowel Diseases Center, University Hospital of the Federal University of Juiz de Fora, School of Medicine of the Federal University of Juiz de Fora, Minas Gerais, Brazil.
Med Sci Monit. 2010 Feb;16(2):PI1-6.
Studies assessing the efficacy of azathioprine (AZA) in steroid-dependent ulcerative colitis (UC) are scarce. The aim of this study was to assess the long-term efficacy and safety of AZA in patients with steroid-dependent UC, as well as factors associated with sustained response.
MATERIAL/METHODS: In this prospective observational study 46 adult subjects with steroid-dependent UC were included for AZA therapy during a 12-month period. AZA dosage was adjusted according to clinical response and occurrence of adverse events. Steroid therapy was tapered according to protocol. The primary endpoint was the rate of steroid-free remission to AZA at the end of 12 months. Secondary endpoints included clinical relapse, cumulative steroid dose and safety of treatment.
On an intention-to-treat basis, the proportion of patients remaining in steroid-free remission at the end of 12 months was 0.54. The median time until complete steroid withdrawal was 5 months. A significant decrease in the relapse rate and in requirement for steroids were observed during 12 months on AZA compared with the prior year (P=0.000). Demographic, dose of AZA, steroid use, and disease-related data did not correlate with remission. Only disease duration <24 months was associated to steroid-free remission (P=0.03, OR 3.60 95% CI 1.95-9.74). Serious adverse events related to AZA were uncommon.
AZA demonstrated sustained efficacy for maintenance of clinical remission without steroids and steroid sparing through 12 months of therapy in steroid-dependent UC. Patients with early onset UC are those who most probably will achieve sustained steroid-free remission while on AZA.
评估硫唑嘌呤(AZA)在激素依赖型溃疡性结肠炎(UC)中的疗效的研究较少。本研究旨在评估 AZA 在激素依赖型 UC 患者中的长期疗效和安全性,以及与持续缓解相关的因素。
材料/方法:在这项前瞻性观察性研究中,46 名成人激素依赖型 UC 患者接受 AZA 治疗,为期 12 个月。根据临床反应和不良反应的发生情况调整 AZA 剂量。根据方案逐渐减少激素治疗。主要终点是在 12 个月时 AZA 达到无激素缓解的比例。次要终点包括临床复发、累积激素剂量和治疗安全性。
根据意向治疗原则,在 12 个月结束时仍处于无激素缓解的患者比例为 0.54。完全停用激素的中位时间为 5 个月。与前一年相比,在接受 AZA 治疗的 12 个月期间,复发率和对激素的需求显著降低(P=0.000)。在接受 AZA 治疗的 12 个月期间,与疾病相关的数据与缓解无关。只有疾病持续时间<24 个月与无激素缓解相关(P=0.03,OR 3.60 95%CI 1.95-9.74)。与 AZA 相关的严重不良事件并不常见。
AZA 在激素依赖型 UC 患者中显示出持续的疗效,可在 12 个月的治疗中维持无激素缓解和节省激素。发病较早的 UC 患者最有可能在接受 AZA 治疗时实现持续的无激素缓解。