Department of Medicine, Lynda K. and David M. Underwood Center for Digestive Disorders, Houston Methodist Hospital, Houston, Texas, USA.
J Dig Dis. 2024 Feb;25(2):91-99. doi: 10.1111/1751-2980.13261.
We aimed to investigate whether vedolizumab (VDZ) levels were associated with inflammatory markers or clinical or endoscopic scoring in inflammatory bowel disease (IBD).
Besides demographic data, clinical scoring, endoscopic data, and laboratory markers of IBD patients treated with VDZ from 2015 to 2020 who had trough levels drawn on maintenance therapy were collected at baseline and at follow-up (after at least 8 weeks on VDZ therapy or after change in dose frequency). Low drug levels were defined as VDZ trough <20 μg/mL.
We identified 89 patients with a mean age of 42.9 years. Of the 90 total trough levels drawn, 61.1% were low. Among patients on every 8 week (Q8 week) VDZ dosing, 81.5% had low troughs. After increasing dosing frequency to Q4 weeks, all patients showed improvement in VDZ levels, but 30.6% remained <20 μg/mL. Higher VDZ levels on Q8 week dosing were associated with higher albumin levels (P = 0.01). While higher VDZ levels on Q4 week dosing were associated with higher albumin (P = 0.02), lower erythrocyte sedimentation rate (P = 0.04) and higher likelihood of having mild disease or endoscopic remission (P = 0.01). No significant association was found between VDZ levels and clinical scoring, body mass index, hemoglobin, vitamin D or platelet levels on either Q8 or Q4 week dosing.
Higher VDZ troughs were associated with higher albumin, mild endoscopic disease or endoscopic remission. Patients who continue to have low VDZ troughs despite Q4 week dosing may require a change in therapy.
我们旨在研究维得利珠单抗(VDZ)水平与炎症标志物或炎症性肠病(IBD)的临床或内镜评分是否相关。
除了人口统计学数据、临床评分、内镜数据和 IBD 患者的实验室标志物外,我们还收集了 2015 年至 2020 年接受 VDZ 治疗的患者的维持治疗时的 VDZ 谷值,这些患者在 VDZ 治疗至少 8 周后或剂量调整后进行了随访(频率改变后)。低药物水平定义为 VDZ 谷值<20μg/ml。
我们确定了 89 名平均年龄为 42.9 岁的患者。在总共 90 个 VDZ 谷值中,61.1%为低值。在所有接受每 8 周(Q8 周)VDZ 给药的患者中,81.5%的患者谷值较低。增加至每 4 周(Q4 周)给药频率后,所有患者的 VDZ 水平均有所改善,但仍有 30.6%<20μg/ml。Q8 周给药时更高的 VDZ 水平与更高的白蛋白水平相关(P=0.01)。而 Q4 周给药时更高的 VDZ 水平与更高的白蛋白(P=0.02)、更低的红细胞沉降率(P=0.04)和更有可能患有轻度疾病或内镜缓解(P=0.01)相关。在 Q8 或 Q4 周给药时,VDZ 水平与临床评分、体重指数、血红蛋白、维生素 D 或血小板水平均无显著相关性。
更高的 VDZ 谷值与更高的白蛋白、轻度内镜疾病或内镜缓解相关。尽管进行了 Q4 周给药,但仍有患者 VDZ 谷值较低,可能需要改变治疗方案。