Division of Gastroenterology, Department of Medicine, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Department for Medical Communication and Translation Studies, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Inflamm Bowel Dis. 2024 May 2;30(5):768-779. doi: 10.1093/ibd/izad135.
Tofacitinib (TFB) appears to be effective in the treatment of ulcerative colitis (UC); however, available real-world studies are limited by cohort size. TFB could be an option in the treatment of acute severe ulcerative colitis (ASUC). We aimed to investigate efficacy and safety of TFB in moderate-to-severe colitis and ASUC.
This retrospective, international cohort study enrolling UC patients with ≥6-week follow-up period was conducted from February 1 to July 31, 2022. Indications were categorized as ASUC and chronic activity (CA). Baseline demographic and clinical data were obtained. Steroid-free remission (SFR), colectomy, and safety data were analyzed.
A total of 391 UC patients (median age 38 [interquartile range, 28-47] years; follow-up period 26 [interquartile range, 14-52] weeks) were included. A total of 27.1% received TFB in ASUC. SFR rates were 23.7% (ASUC: 26.0%, CA: 22.8%) at week 12 and 41.1% (ASUC: 34.2%, CA: 43.5%) at week 52. The baseline partial Mayo score (odds ratio [OR], 0.850; P = .006) was negatively associated with week 12 SFR, while biologic-naïve patients (OR, 2.078; P = .04) more likely achieved week 52 SFR. The colectomy rate at week 52 was higher in ASUC group (17.6% vs 5.7%; P < .001) and decreased with age (OR, 0.94; P = .013). A total of 67 adverse events were reported, and 17.9% resulted in cessation of TFB. One case of thromboembolic event was reported.
TFB is effective in both studied indications. TFB treatment resulted in high rates of SFR in the short and long terms. Higher baseline disease activity and previous biological therapies decreased efficacy. No new adverse event signals were found.
托法替布(TFB)似乎对溃疡性结肠炎(UC)的治疗有效;然而,现有的真实世界研究受到队列规模的限制。TFB 可能是治疗急性重度溃疡性结肠炎(ASUC)的一种选择。我们旨在研究 TFB 在中重度结肠炎和 ASUC 中的疗效和安全性。
这是一项回顾性的国际队列研究,纳入了有≥6 周随访期的 UC 患者,研究于 2022 年 2 月 1 日至 7 月 31 日进行。指征分为 ASUC 和慢性活动(CA)。收集基线人口统计学和临床数据。分析了类固醇无缓解(SFR)、结肠切除术和安全性数据。
共纳入 391 例 UC 患者(中位年龄 38 [四分位距 28-47] 岁;随访期 26 [四分位距 14-52] 周)。ASUC 中有 27.1%的患者接受了 TFB 治疗。第 12 周 SFR 率分别为 23.7%(ASUC:26.0%,CA:22.8%)和第 52 周 41.1%(ASUC:34.2%,CA:43.5%)。基线部分 Mayo 评分(比值比 [OR],0.850;P=0.006)与第 12 周 SFR 呈负相关,而生物初治患者(OR,2.078;P=0.04)更有可能在第 52 周达到 SFR。第 52 周结肠切除术率在 ASUC 组较高(17.6%比 5.7%;P<0.001),并随年龄增长而降低(OR,0.94;P=0.013)。共报告了 67 例不良事件,17.9%的患者因 TFB 停药。报告了 1 例血栓栓塞事件。
TFB 在这两种研究指征中均有效。TFB 治疗在短期和长期均产生了较高的 SFR 率。较高的基线疾病活动度和既往生物治疗降低了疗效。未发现新的不良事件信号。