Third Department of Internal Medicine, University of Occupational and Environmental Health, School of Medicine, Japan.
Department of Gastroenterology, Ashiya Central Hospital, Japan.
Intern Med. 2021 Dec 15;60(24):3849-3856. doi: 10.2169/internalmedicine.7279-21. Epub 2021 Jun 12.
Objective Real-world data of adalimumab (ADA) in the treatment of ulcerative colitis (UC) are scarce. We aimed to study the ADA response rates and predictors of response in UC treatment. Methods This observational, prospective and multi-center study assessed the clinical outcome of refractory UC patients treated with ADA who previously had an inadequate response to either conventional therapies or other anti-TNF antibodies or tacrolimus. The primary endpoint was the proportion of UC patients achieving a clinical response and remission at 8 and 52 weeks. We also evaluated the parameters which were associated with a clinical response at 8 and 52 weeks. Results A total of 35 patients were enrolled from 11 centers. The clinical responses at 8 and 52 weeks were 60.0% and 51.4%, respectively. The clinical remission rates at 8 and 52 weeks were 45.7% and 48.6%, respectively. Positive predictors for week 52 response were combination of ADA with immunomodulator (IM) (OR: 27.229; 95% CI; 1.897-390.76; p=0.015) and a week 8 lower partial Mayo score (OR: 0.406; 95% CI; 0.204-0.809; p=0.010). A receiver operation characteristic curve analysis revealed the optimal week 8 partial Mayo score to be 2.5, therefore a partial Mayo score of ≤2 was a positive predictor for the continuation of ADA. No malignancy or death occurred during this study. Conclusion ADA was effective for inducing and maintaining both a clinical response and remission in patients with refractory UC. It remains possible that the concomitant use of IM and a week 8 partial Mayo score of ≤2 may predict the long-term response of ADA.
阿达木单抗(ADA)治疗溃疡性结肠炎(UC)的真实世界数据较为匮乏。本研究旨在探讨 ADA 治疗 UC 的应答率及其应答预测因素。
本观察性、前瞻性、多中心研究评估了先前对常规治疗或其他抗 TNF 抗体或他克莫司应答不足的难治性 UC 患者接受 ADA 治疗的临床结局。主要终点为治疗 8 周和 52 周时达到临床缓解和缓解的 UC 患者比例。我们还评估了与治疗 8 周和 52 周时临床应答相关的参数。
本研究共纳入了来自 11 个中心的 35 例患者。治疗 8 周和 52 周时的临床应答率分别为 60.0%和 51.4%,临床缓解率分别为 45.7%和 48.6%。52 周时应答的阳性预测因素为 ADA 联合免疫调节剂(IM)(OR:27.229;95%CI;1.897-390.76;p=0.015)和第 8 周较低的部分 Mayo 评分(OR:0.406;95%CI;0.204-0.809;p=0.010)。受试者工作特征曲线分析显示,第 8 周部分 Mayo 评分最佳截断值为 2.5,因此部分 Mayo 评分≤2 是 ADA 继续治疗的阳性预测因素。本研究期间未发生恶性肿瘤或死亡。
ADA 可有效诱导和维持难治性 UC 患者的临床缓解和缓解。同时使用 IM 和第 8 周部分 Mayo 评分≤2 可能预测 ADA 的长期应答。