Efficacy of biological therapies and small molecules in induction and maintenance of remission in luminal Crohn's disease: systematic review and network meta-analysis

被引:111
作者
Barberio, Brigida [1 ]
Gracie, David J. [2 ]
Black, Christopher J. [2 ]
Ford, Alexander C. [2 ,3 ]
机构
[1] Univ Padua, Dept Surg Oncol & Gastroenterol, Padua, Italy
[2] Leeds Teaching Hosp NHS Trust, Leeds Gastroenterol Inst, Leeds, W Yorkshire, England
[3] Univ Leeds, Leeds Inst Med Res St Jamess, Leeds, W Yorkshire, England
关键词
crohn's disease; meta-analysis; CERTOLIZUMAB PEGOL; ADALIMUMAB INDUCTION; CLINICAL REMISSION; JAPANESE PATIENTS; CONTROLLED-TRIAL; DOUBLE-BLIND; INFLIXIMAB; USTEKINUMAB; VEDOLIZUMAB; 5-AMINOSALICYLATES;
D O I
10.1136/gutjnl-2022-328052
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective There are numerous biological therapies and small molecules licensed for luminal Crohn's disease (CD), but these are often studied in placebo-controlled trials, meaning relative efficacy is uncertain. We examined this in a network meta-analysis. Design We searched the literature to 1 July 2022, judging efficacy according to induction of clinical remission, clinical response and maintenance of clinical remission, and according to previous exposure or non-exposure to biologics. We used a random effects model and reported data as pooled relative risks (RRs) with 95% CIs, ranking drugs according to p-score. Results We identified 25 induction of remission trials (8720 patients). Based on failure to achieve clinical remission, infliximab 5 mg/kg ranked first versus placebo (RR=0.67, 95% CI 0.56 to 0.79, p-score 0.95), with risankizumab 600 mg second and upadacitinib 45 mg once daily third. However, risankizumab 600 mg ranked first for clinical remission in biologic-naive (RR=0.66, 95% CI 0.52 to 0.85, p-score 0.78) and in biologic-exposed patients (RR=0.74, 95% CI 0.67 to 0.82, p-score 0.92). In 15 maintenance of remission trials (4016 patients), based on relapse of disease activity, upadacitinib 30 mg once daily ranked first (RR=0.61, 95% CI 0.52 to 0.72, p-score 0.93) with adalimumab 40 mg weekly second, and infliximab 10 mg/kg 8-weekly third. Adalimumab 40 mg weekly ranked first in biologic-naive patients (RR=0.59, 95% CI 0.48 to 0.73, p-score 0.86), and vedolizumab 108 mg 2-weekly first in biologic-exposed (RR=0.70, 95% CI 0.57 to 0.86, p-score 0.82). Conclusion In a network meta-analysis, infliximab 5 mg/kg ranked first for induction of clinical remission in all patients with luminal CD, but risankizumab 600 mg was first in biologic-naive and biologic-exposed patients. Upadacitinib 30 mg once daily ranked first for maintenance of remission.
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页码:264 / 274
页数:11
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