Department of Gastroenterology and Hepatology, AGEM Research Institute, Amsterdam University Medical Centre, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Teva Pharmaceutical Industries, Haarlem, The Netherlands.
J Crohns Colitis. 2023 Jun 16;17(6):933-942. doi: 10.1093/ecco-jcc/jjad013.
Thioguanine is a well-tolerated and effective therapy for inflammatory bowel disease [IBD] patients. Prospective effectiveness data are needed to substantiate the role of thioguanine as a maintenance therapy for IBD.
IBD patients who previously failed azathioprine or mercaptopurine and initiated thioguanine were prospectively followed for 12 months starting when corticosteroid-free clinical remission was achieved (Harvey-Bradshaw Index [HBI] ≤ 4 or Simple Clinical Colitis Activity Index [SCCAI] ≤ 2). The primary endpoint was corticosteroid-free clinical remission throughout 12 months. Loss of clinical remission was defined as SCCAI > 2 or HBI > 4, need of surgery, escalation of therapy, initiation of corticosteroids or study discontinuation. Additional endpoints were adverse events, drug survival, physician global assessment [PGA] and quality of life [QoL].
Sustained corticosteroid-free clinical remission at 3, 6 or 12 months was observed in 75 [69%], 66 [61%] and 49 [45%] of 108 patients, respectively. Thioguanine was continued in 86 patients [80%] for at least 12 months. Loss of response [55%] included escalation to biologicals in 15%, corticosteroids in 10% and surgery in 3%. According to PGA scores, 82% of patients were still in remission after 12 months and QoL scores remained stable. Adverse events leading to discontinuation were reported in 11%, infections in 10%, myelo- and hepatotoxicity each in 6%, and portal hypertension in 1% of patients.
Sustained corticosteroid-free clinical remission over 12 months was achieved in 45% of IBD patients on monotherapy with thioguanine. A drug continuation rate of 80%, together with favourable PGA and QoL scores, underlines the tolerability and effectiveness of thioguanine for IBD.
硫鸟嘌呤是一种耐受良好且有效的炎症性肠病[IBD]治疗药物。需要前瞻性的有效性数据来证实硫鸟嘌呤作为 IBD 维持治疗的作用。
本研究前瞻性地随访了 108 例先前对巯嘌呤或巯基嘌呤治疗失败并开始使用硫鸟嘌呤的 IBD 患者,随访时间从达到无皮质类固醇临床缓解时(Harvey-Bradshaw 指数[HBI]≤4 或简单临床结肠炎活动指数[SCCAI]≤2)开始,共 12 个月。主要终点是 12 个月内无皮质类固醇的临床缓解。临床缓解丧失定义为 SCCAI>2 或 HBI>4、需要手术、治疗升级、开始使用皮质类固醇或研究中止。其他终点包括不良事件、药物生存、医生整体评估[PGA]和生活质量[QoL]。
108 例患者中,分别有 75 例(69%)、66 例(61%)和 49 例(45%)在 3、6 和 12 个月时持续达到无皮质类固醇的临床缓解。86 例(80%)患者至少使用硫鸟嘌呤治疗 12 个月。有 55%的患者发生应答丧失,其中 15%的患者升级为生物制剂,10%的患者使用皮质类固醇,3%的患者接受手术。根据 PGA 评分,12 个月后仍有 82%的患者处于缓解状态,QoL 评分保持稳定。有 11%的患者因不良事件停药,10%的患者发生感染,6%的患者发生骨髓和肝毒性,1%的患者发生门静脉高压。
在接受硫鸟嘌呤单药治疗的 IBD 患者中,有 45%的患者在 12 个月时达到无皮质类固醇的临床缓解。80%的药物持续率,加上良好的 PGA 和 QoL 评分,突显了硫鸟嘌呤治疗 IBD 的耐受性和有效性。