Section of Gastroenterology, University of Manitoba, Winnipeg, MB, R3E 3P4, Canada. Center of Global Public Health, University of Manitoba, Winnipeg, MB, R3E 3P4, Canada. Department of Community Health Sciences, University of Manitoba, Winnipeg, MB, R3E 3P4, Canada.
Am J Gastroenterol. 2018 Aug;113(8):1206-1216. doi: 10.1038/s41395-018-0108-6. Epub 2018 Jun 21.
Immunomodulator (IM)-based monotherapy with thiopurines or methotrexate is being increasingly supplanted in the management of moderate-to-severe IBD by more efficacious biologic agents. However, given their low cost, IMs may still have a selective role in this setting.
We used a Canadian population-based dataset of persons with IBD spanning from 1996 until 2014 to assess the initiation and continued use of IM monotherapy, the incidence of outcomes associated with ineffectiveness (defined as IBD-related hospitalization, IBD-resective surgery, systemic corticosteroid (CS) use, or the need for biologic therapy), and the demographic and disease-related characteristics associated with persistence on IM monotherapy and IBD-associated adverse outcomes.
There were 3312 persons diagnosed with IBD (1480 CD, 1832 ulcerative colitis (UC)) in the study period. The cumulative incidence of IM monotherapy use at 5 years was 46 % for CD and 24.9% for UC. Approximately one-third remained on IM monotherapy continuously for 5 years or more. Roughly three-quarters of IM users with a history of corticosteroid use had at least a 50% reduction in corticosteroid exposure in the year following IM initiation. Thirty-five percent of those with CD and 30% with UC had not developed evidence of therapeutic ineffectiveness within 5 years of IM initiation; people with no history of prior corticosteroid use, no IBD hospitalizations, and persons with CD initiating IM therapy after age 40 were less likely to have an episode of therapeutic ineffectiveness while on IM monotherapy CONCLUSIONS: Although the majority of persons who are initiated on IM monotherapy discontinue medications and/or have evidence of therapeutic ineffectiveness a significant minority remain free of these outcomes over many years of therapy.
免疫调节剂(IM)为基础的硫唑嘌呤或甲氨蝶呤单药治疗在中重度 IBD 的管理中越来越被更有效的生物制剂所取代。然而,鉴于其低成本,IM 可能仍然在这种情况下具有选择性作用。
我们使用了一个加拿大基于人群的 IBD 患者数据集,该数据集涵盖了 1996 年至 2014 年的时间,以评估 IM 单药治疗的起始和持续使用、与无效相关的结局(定义为 IBD 相关住院、IBD 切除术、全身皮质类固醇(CS)使用或生物治疗的需要)的发生率,以及与 IM 单药治疗和 IBD 相关不良结局相关的人口统计学和疾病相关特征。
在研究期间,有 3312 人被诊断为 IBD(1480 例 CD,1832 例溃疡性结肠炎(UC))。CD 的 IM 单药治疗 5 年累积发生率为 46%,UC 为 24.9%。大约三分之一的人连续 5 年或更长时间继续使用 IM 单药治疗。大约四分之三的 IM 使用者在开始使用 IM 后一年内皮质类固醇暴露量至少减少了 50%。35%的 CD 患者和 30%的 UC 患者在开始 IM 治疗后 5 年内没有出现治疗无效的证据;没有皮质类固醇使用史、没有 IBD 住院史且 40 岁以后开始 IM 治疗的人在 IM 单药治疗期间发生治疗无效的可能性较小。
尽管大多数开始接受 IM 单药治疗的患者停止了治疗药物,或出现了治疗无效的证据,但仍有相当一部分患者在多年的治疗中没有出现这些结局。