Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Box 281, 171 77, Stockholm, Sweden.
Department of Biomedical and Clinical Sciences, Division of Surgery, Linköping University Hospital, Linköping University, Linköping, Sweden.
Dig Dis Sci. 2023 Jan;68(1):65-76. doi: 10.1007/s10620-022-07501-z. Epub 2022 Apr 22.
Prospectively and systematically collected long-term real-world clinical data on ustekinumab (anti-interleukin-12/23) are still scarce.
To assess the long-term effectiveness of ustekinumab in patients with active Crohn's disease (CD).
This is a prospective multicenter study of adult patients with CD initiating ustekinumab according to recommended doses at 20 Swedish hospitals. The primary outcome was clinical remission (Harvey-Bradshaw Index (HBI) ≤ 4 points) at weeks 52 and 104. Secondary outcomes included clinical response (≥ 3-point-decrease in HBI among patients with initial HBI ≥ 5 points), treatment retention, and biomarkers (C-reactive protein (CRP), hemoglobin, fecal-calprotectin) at weeks 52 and 104 compared to baseline. We also reported Health-related Quality of Life (HRQoL) measures.
Of 114 included patients, 107 (94%) had previously failed ≥ 1 and 58 (51%) ≥ 2 anti-tumor necrosis factor agents. Forty (35%) had failed anti-integrin agents. Ustekinumab retention rates at weeks 52 and 104 were 70% (n = 80/114) and 61% (n = 69/114), respectively. Clinical response was seen in 36% (n = 25/69) and 29% (n = 20/69) of the patients, and remission was achieved in 32% (n = 31/96) and 29% (n = 28/96) at weeks 52 and 104, respectively. Median HBI and CRP levels decreased significantly at both timepoints as compared to baseline. Significant improvements were also observed in HRQoL. Adverse events were reported in 11% (n = 13/114) of the patients, including five cases of severe adverse events. No malignancies were observed.
In this nationwide prospective real-world 104-week-follow-up study of adult patients with active CD, ustekinumab was associated with long-term clinical effectiveness and improvement in HRQoL measures when used in routine clinical care.
关于乌司奴单抗(抗白细胞介素-12/23)的长期真实世界临床数据仍十分有限。
评估乌司奴单抗治疗活动期克罗恩病(CD)患者的长期疗效。
这是一项在瑞典 20 家医院开展的前瞻性多中心研究,纳入了起始接受乌司奴单抗治疗的 CD 成年患者。主要结局为第 52 周和第 104 周时的临床缓解(Harvey-Bradshaw 指数(HBI)≤4 分)。次要结局包括第 52 周和第 104 周时与基线相比的临床应答(HBI 初始值≥5 分的患者中 HBI 下降≥3 分)、治疗保留率以及生物标志物(C 反应蛋白(CRP)、血红蛋白、粪便钙卫蛋白)。我们还报告了健康相关生活质量(HRQoL)测量结果。
114 例纳入患者中,107 例(94%)曾接受过≥1 种抗 TNF 药物治疗失败,58 例(51%)曾接受过≥2 种抗 TNF 药物治疗失败,58 例(51%)曾接受过抗整合素药物治疗失败。乌司奴单抗治疗保留率在第 52 周和第 104 周分别为 70%(n=80/114)和 61%(n=69/114)。第 52 周和第 104 周时,患者的临床应答率分别为 36%(n=25/69)和 29%(n=20/69),缓解率分别为 32%(n=28/96)和 29%(n=28/96)。与基线相比,HBI 和 CRP 中位数在两个时间点均显著下降,HRQoL 也显著改善。11%(n=13/114)的患者报告发生了不良事件,包括 5 例严重不良事件。未观察到恶性肿瘤。
在这项针对活动期 CD 成年患者的全国性前瞻性 104 周随访研究中,乌司奴单抗在常规临床治疗中与长期临床疗效和 HRQoL 改善相关。