UGC Aparato Digestivo, Hospital Universitario Virgen Macarena, España.
Aparato Digestivo, Hospital Universitario Virgen Macarena, España.
Rev Esp Enferm Dig. 2022 May;114(5):272-279. doi: 10.17235/reed.2020.7352/2020.
ustekinumab is a monoclonal antibody that inhibits interleukins IL-12 and IL-23, and is approved for the treatment of Crohn's disease (CD) and, more recently, also ulcerative colitis (UC). The aim of this study was to evaluate the effectiveness and safety of ustekinumab, as well as to identify possible predictive factors of response in a real-life setting.
an observational, retrospective, multicenter study was carried out in 4 hospitals in Andalusia. Adult patients with a confirmed diagnosis of CD treated with ustekinumab from 2017 to 2019 were included. Clinical response was analyzed at 3, 6 and 12 months of treatment. Clinical disease activity was assessed with the Harvey-Bradshaw index (HBI) and the Crohn's Disease Activity Index (CDAI); biochemical response was assessed with lab parameters such as CRP and ESR. One-year ustekinumab drug-survival was analyzed.
a total of 98 patients were analyzed (mean age, 43 years; 52 % were male); 56 % had failed with ≥ 2 previous biologicals therapies. At 3 months, 69 % of the patients were in response and 40.8 % in remission. At 6 months, 56 % were in clinical remission. At 12 months, 73.7 % were in clinical response and 60.5 % in remission. Corticosteroid-free remission was 32.4 %, 44 %, and 47.4 % at 3, 6, and 12 months, respectively. Cumulative survival after one year of treatment with ustekinumab was 85.3 %. Biochemical parameters such as CRP and ESR showed a statistically significant decrease between baseline and control levels at 3, 6, and 12 months. A lower HBI at baseline and female sex were predictors of corticosteroid-free clinical remission in a univariate analysis. In the multivariate analysis no variables were found as predictors of corticosteroid-free clinical remission.
ustekinumab therapy is safe and useful, inducing clinical response in more than 50 % of patients, including patients who failed with other biological therapies.
乌司奴单抗是一种单克隆抗体,可抑制白细胞介素-12 和白细胞介素-23,已获批准用于治疗克罗恩病(CD),最近也用于治疗溃疡性结肠炎(UC)。本研究旨在评估乌司奴单抗在真实环境中的疗效和安全性,并确定可能的应答预测因素。
在安达卢西亚的 4 家医院进行了一项观察性、回顾性、多中心研究。纳入了 2017 年至 2019 年期间接受乌司奴单抗治疗的确诊为 CD 的成年患者。在治疗的第 3、6 和 12 个月分析临床应答。临床疾病活动度采用 Harvey-Bradshaw 指数(HBI)和克罗恩病活动指数(CDAI)评估;生化应答采用 CRP 和 ESR 等实验室参数评估。分析了乌司奴单抗的 1 年药物生存率。
共分析了 98 例患者(平均年龄 43 岁;52%为男性);56%的患者之前已接受过≥2 种生物制剂治疗但失败。在第 3 个月时,69%的患者有应答,40.8%的患者缓解。在第 6 个月时,56%的患者处于临床缓解。在第 12 个月时,73.7%的患者有临床应答,60.5%的患者缓解。第 3、6 和 12 个月时无皮质类固醇缓解的分别为 32.4%、44%和 47.4%。乌司奴单抗治疗 1 年后的累积生存率为 85.3%。CRP 和 ESR 等生化参数在第 3、6 和 12 个月时与基线相比均有统计学显著下降。单因素分析显示,基线时较低的 HBI 和女性是无皮质类固醇临床缓解的预测因素。多因素分析未发现无皮质类固醇临床缓解的预测因素。
乌司奴单抗治疗安全有效,可使超过 50%的患者产生临床应答,包括那些对其他生物制剂治疗失败的患者。