Department of Gastroenterology and Human Nutrition, All India Institute of Medical Sciences, New Delhi, India.
Department of Radio Diagnosis, All India Institute of Medical Sciences, New Delhi, India.
J Gastroenterol Hepatol. 2022 Aug;37(8):1544-1553. doi: 10.1111/jgh.15880. Epub 2022 May 10.
Thiopurines are widely used to maintain remission in both ulcerative colitis (UC) and Crohn's disease (CD). Reported effectiveness and tolerability rates have been variable across studies. There are only sparse data in Asian population regarding the long-term efficacy and safety of thiopurines.
Records of 5351 patients followed up at inflammatory bowel disease (IBD) clinic, All India Institute of Medical Sciences, New Delhi from 2004 to 2020 were evaluated retrospectively. Safety was evaluated in terms of long-term adverse events and development of malignancy.
Of 5351 patients with IBD, 1093 who received thiopurine for > 3 months (UC = 788 [proctitis-1.9%, left-sided colitis-44.9%, & pancolitis-53.1%] & CD = 305 [inflammatory-42.6%, stricturing-46.9%, & fistulizing-10.5%]) were included (60.8%-male patients). Follow up and treatment duration on thiopurine were 7 (4-12) years and 39.4 ± 40.3 months, respectively, with 254 (23.2%) patients receiving thiopurines for more than 5 and 68 (6.2%) receiving for more than 10 years. Three hundred and fifty-nine (UC: 249 [31.6%]; CD: 110 [36.1%]; P = 0.1) patients developed adverse events; commonest was myelosuppression (23.4%) followed by gastrointestinal intolerance (3%), flu-like illness (1.7%), and arthralgia/myalgia (1.4%). Myelosuppression was the commonest cause of thiopurine withdrawal. No patient (including 254 patients on thiopurine for ≥ 5 years) developed lymphoma or non-melanoma skin cancer. The cumulative probability of staying free from adverse events in overall IBD cohort at 1, 2, and 5 years was 78.6%, 71.9%, and 68.4%, respectively, and this was comparable between UC and CD (P = 0.09).
Long-term follow up of patients with IBD from northern India on thiopurine monotherapy demonstrated minimal risk of development of lymphoma as well as non-melanoma skin cancer.
硫嘌呤广泛用于溃疡性结肠炎(UC)和克罗恩病(CD)的缓解维持。不同研究的报告有效性和耐受性存在差异。亚洲人群关于硫嘌呤的长期疗效和安全性的数据很少。
回顾性评估了 2004 年至 2020 年在全印度医学科学院炎症性肠病(IBD)诊所就诊的 5351 例患者的记录。安全性评估包括长期不良事件和恶性肿瘤的发生。
在 5351 例 IBD 患者中,1093 例接受硫嘌呤治疗>3 个月(UC=788 [直肠炎-1.9%,左结肠炎-44.9%,全结肠炎-53.1%]和 CD=305 [炎症-42.6%,狭窄-46.9%,瘘管-10.5%])(60.8%-男性患者)。硫嘌呤的随访和治疗时间分别为 7(4-12)年和 39.4±40.3 个月,254 例(23.2%)患者接受硫嘌呤治疗超过 5 年,68 例(6.2%)患者接受硫嘌呤治疗超过 10 年。359 例(UC:249 [31.6%];CD:110 [36.1%];P=0.1)患者出现不良反应;最常见的是骨髓抑制(23.4%),其次是胃肠道不耐受(3%)、流感样疾病(1.7%)和关节痛/肌痛(1.4%)。骨髓抑制是硫嘌呤停药的最常见原因。无患者(包括 254 例接受硫嘌呤治疗≥5 年的患者)发生淋巴瘤或非黑色素瘤皮肤癌。总体 IBD 队列中,1、2、5 年无不良反应的累积概率分别为 78.6%、71.9%和 68.4%,UC 和 CD 之间无差异(P=0.09)。
来自印度北部的 IBD 患者长期接受硫嘌呤单药治疗,发生淋巴瘤和非黑色素瘤皮肤癌的风险极小。