Real-world Evidence Comparing Tofacitinib and Vedolizumab in Anti-TNF-experienced Patients With Ulcerative Colitis

被引:0
|
作者
Adimadhyam, Sruthi [1 ,2 ]
Lewis, James D. [3 ,4 ]
Simon, Andrew L. [1 ,2 ]
Wolfe, Audrey E. [1 ,2 ]
Smith, Samantha [1 ,2 ]
Hou, Laura [1 ,2 ]
Moyneur, Erick [5 ]
Reynolds, Juliane S. [1 ,2 ]
Toh, Sengwee [1 ,2 ]
Dobes, Angela [6 ]
Parlett, Lauren [7 ]
Haynes, Kevin [7 ]
Burris, Jessica [8 ]
Dorand, Jennifer E. [6 ]
Long, Millie D. [9 ]
Kappelman, Michael D. [9 ,10 ]
机构
[1] Harvard Med Sch, Dept Populat Med, Boston, MA USA
[2] Harvard Pilgrim Hlth Care Inst, Boston, MA USA
[3] Univ Penn, Dept Med, Div Gastroenterol & Hepatol, Perelman Sch Med, Philadelphia, PA USA
[4] Univ Penn, Perelman Sch Med, Dept Biostat Epidemiol & Informat, Philadelphia, PA USA
[5] StatLog Econometr Inc, Montreal, PQ, Canada
[6] Crohns & Colitis Fdn, New York, NY USA
[7] Carelon Res, Wilmington, DE USA
[8] Yale Univ, Sch Med, New Haven, CT USA
[9] Univ North Carolina Chapel Hill, Chapel Hill, NC USA
[10] Univ North Carolina Chapel Hill, Campus Box 7229,Bioinformat Bldg,130 Mason Farm Rd, Chapel Hill, NC 27599 USA
关键词
ulcerative colitis; comparative effectiveness; tofacitinib; vedolizumab; MAINTENANCE THERAPY; VALIDATION; INDUCTION; EXPOSURE; SCORE;
D O I
10.1093/ibd/izad115
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Antitumor necrosis factor (anti-TNF) inhibitors are first-line treatment among patients with ulcerative colitis (UC). With time, patients tend to lose response or become intolerant, necessitating switching to small cell biologics such as tofacitinib or vedolizumab. In this real-world study of a large, geographically diverse US population of TNF-experienced patients with UC, we evaluated the effectiveness and safety of newly initiating treatment with tofacitinib vs vedolizumab. Methods We conducted a cohort study using secondary data from a large US insurer (Anthem, Inc.). Our cohort included patients with UC newly initiating treatment with tofacitinib or vedolizumab. Patients were required to have evidence of treatment with anti-TNF inhibitors in the 6 months prior to cohort entry. The primary outcome was treatment persistence >52 weeks. Additionally, we evaluated the following secondary outcomes as additional measures of effectiveness and safety: (1) all-cause hospitalization; (2) total abdominal colectomy; (3) hospitalization for infection; (4) hospitalization for malignancy; (5) hospitalization for cardiac events; and (6) hospitalization for thromboembolic events. We used fine stratification by propensity scores to control for confounding by demographics, clinical factors, and treatment history at baseline. Results Our primary cohort included 168 new users of tofacitinib and 568 new users of vedolizumab. Tofacitinib was associated with lower treatment persistence (adjusted risked ratio, 0.77; 95% CI, 0.60 -0.99). Differences in secondary measures of effectiveness or safety between tofacitinib initiators vs vedolizumab initiators were not statistically significant (all-cause hospitalization, adjusted hazard ratio, 1.23; 95% CI, 0.83-1.84; total abdominal colectomy, adjusted HR, 1.79; 95% CI, 0.93-3.44;and hospitalization for any infection, adjusted HR, 1.94; 95% CI, 0.83-4.52). Discussion Ulcerative colitis patients with prior anti-TNF experience initiating tofacitinib demonstrated lower treatment persistence compared with those initiating vedolizumab. This finding is in contrast to other recent studies suggesting superior effectiveness of tofacitinib. Ultimately, head-to-head randomized, controlled trials that focus on directly measured end points may be needed to best inform clinical practice. Lay Summary Anti-TNF-experienced patients with UC initiating vedolizumab demonstrated higher treatment persistence compared with those initiating tofacitinib in this real-world evaluation of comparative effectiveness. Ultimately, head-to-head randomized trials that focus on directly measured end points are needed to best inform clinical practice.
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收藏
页码:554 / 562
页数:9
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