Tofacitinib for Biologic-Experienced Hospitalized Patients With Acute Severe Ulcerative Colitis: A Retrospective Case-Control Study.

Tofacitinib for Biologic-Experienced Hospitalized Patients With Acute Severe Ulcerative Colitis: A Retrospective Case-Control Study.
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用于生物经验的急性严重溃疡性结肠炎患者的tofacitib:一项回顾性病例对照研究。

DOI:
10.1016/j.cgh.2021.05.038
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发表时间:
2021-10
期刊:
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association
影响因子:
--
通讯作者:
Higgins PDR
Higgins PDR
中科院分区:
其他
文献类型:
--
作者:
Berinstein JA;Sheehan JL;Dias M;Berinstein EM;Steiner CA;Johnson LA;Regal RE;Allen JI;Cushing KC;Stidham RW;Bishu S;Kinnucan JAR;Cohen-Mekelburg SA;Waljee AK;Higgins PDR

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Despite rescue therapy, more than 30% of patients with acute severe ulcerative colitis (ASUC) require colectomy. Tofacitinib is a rapidly acting JAK inhibitor with proven efficacy in ulcerative colitis. Tofacitinib may provide additional means for preventing colectomy in patients with ASUC. A retrospective case-control study was performed evaluating the efficacy of tofacitinib induction in biologic-experienced patients admitted with ASUC requiring IV corticosteroids. Tofacitinib patients were matched 1:3 to controls according to gender and date of admission. Using Cox regression adjusted for disease severity, we estimated the 90-day risk of colectomy. Rates of complications and steroid dependence were examined as secondary outcomes. Forty patients who received tofacitinib were matched 1:3 to controls (n=113). Tofacitinib was protective against colectomy at 90 days compared to matched controls (HR 0.28, 95% CI 0.10, 0.81, P = 0.018). When stratifying according to treatment dose, 10mg three times daily (HR 0.11 95% CI 0.02, 0.56, P=0.008) was protective, while 10mg twice daily was not significantly protective (HR 0.66, 95% CI 0.21, 2.09, P=0.5). Rate of complications and steroid dependence were similar between tofacitinib and controls. Tofacitinib with concomitant IV corticosteroids may be an effective induction strategy in biologic-experienced patients hospitalized with ASUC. Prospective trials are needed to identify the safety, optimal dose, frequency, and duration of tofacitinib for ASUC.
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