Taxonera Carlos, Olivares David, Alba Cristina
From the Inflammatory Bowel Disease Unit, Gastroenterology Department, Hospital Clínico San Carlos and Instituto de Investigación del Hospital Clínico San Carlos, Madrid, Spain.
Inflamm Bowel Dis. 2022 Jan 5;28(1):32-40. doi: 10.1093/ibd/izab011.
Knowledge of the real-world effectiveness and safety of tofacitinib for ulcerative colitis (UC) is relevant to confirm the benefit observed in clinical trials.
This systematic review and meta-analysis evaluated the real-world effectiveness of tofacitinib for moderate to severely active UC. The primary outcome was clinical remission evaluated at week 8, weeks 12 to 16, and month 6. Secondary outcomes were response, corticosteroid-free remission, mucosal healing, colectomy, and safety.
Seventeen studies with a total of 1162 patients with UC were included. Remission (11 studies) was achieved in 34.7% of patients at week 8 (95% confidence interval [CI], 24.4%-45.1%), 47% at weeks 12 to 16 (95% CI, 40.3%-53.6%), and 38.3% at month 6 (95% CI, 29.2%-47.5%) at month 6 duplicated. Response was achieved in 62.1%, 64.2%, 50.8%, and 41.8% of patients at week 8, weeks 12 to 16, month 6, and month 12, respectively. Corticosteroid-free remission (5 studies) was achieved in 38.4%, 44.3%, 33.6%, and 31% of patients at week 8, weeks 12 to 16, month 6, and month 12, respectively. Mucosal healing was achieved in 48.3% and 45.3% of patients at week 8 and weeks 12 to 16, respectively. Patients who were biologic-naïve (11.6%) had a significantly higher rate of response at week 8 (1.38; 95% CI, 1.03-1.84). The incidence rates of serious adverse events and herpes zoster was 8.9 and 6.9 per 100 patient-years, respectively.
This meta-analysis of real-world studies confirms the effectiveness of tofacitinib in a highly refractory population of patients with moderate to severely active UC. Tofacitinib showed an acceptable safety profile. These findings were consistent with clinical trials and further support the use of tofacitinib in UC.
了解托法替布治疗溃疡性结肠炎(UC)的真实疗效和安全性对于确认临床试验中观察到的益处至关重要。
本系统评价和荟萃分析评估了托法替布治疗中度至重度活动性UC的真实疗效。主要结局是在第8周、第12至16周和第6个月评估的临床缓解。次要结局包括缓解、无皮质类固醇缓解、黏膜愈合、结肠切除术和安全性。
纳入了17项研究,共1162例UC患者。在第8周,34.7%的患者实现缓解(11项研究)(95%置信区间[CI],24.4%-45.1%);在第12至16周,47%的患者实现缓解(95%CI,40.3%-53.6%);在第6个月,38.3%的患者实现缓解(95%CI,29.2%-47.5%)。在第8周、第12至16周、第6个月和第12个月,分别有62.1%、64.2%、50.8%和41.8%的患者获得缓解。在第8周、第12至16周、第6个月和第12个月,分别有38.4%、44.3%、33.6%和31%的患者实现无皮质类固醇缓解(5项研究)。在第8周和第12至16周,分别有48.3%和45.3%的患者实现黏膜愈合。初治生物制剂的患者(11.6%)在第8周的缓解率显著更高(1.38;95%CI,1.03-1.84)。严重不良事件和带状疱疹的发生率分别为每100患者年8.9例和6.9例。
这项对真实世界研究的荟萃分析证实了托法替布在中度至重度活动性UC高度难治患者群体中的有效性。托法替布显示出可接受的安全性。这些发现与临床试验一致,并进一步支持托法替布在UC中的应用。