Vedolizumab serum trough concentrations with and without thiopurines in ulcerative colitis: The prospective VIEWS pharmacokinetics study.

IF 4.3 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY World Journal of Gastroenterology Pub Date : 2025-01-14 DOI:10.3748/wjg.v31.i2.101292
Thanaboon Chaemsupaphan, Aviv Pudipeddi, Hui-Yu Lin, Sudarshan Paramsothy, Viraj C Kariyawasam, Melissa Kermeen, Rupert W Leong
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Abstract

Background: Ulcerative colitis (UC) is a chronic inflammatory condition requiring continuous treatment and monitoring. There is limited pharmacokinetic data on vedolizumab during maintenance therapy and the effect of thiopurines on vedolizumab trough concentrations is unknown.

Aim: To investigate the exposure-response relationship of vedolizumab and the impact of thiopurine withdrawal in UC patients who have achieved sustained clinical and endoscopic remission during maintenance therapy.

Methods: This is a post-hoc analysis of prospective randomized clinical trial (VIEWS) involving UC patients across 8 centers in Australia from 2018 to 2022. Patients in clinical and endoscopic remission were randomized to continue or withdraw thiopurine while receiving vedolizumab. We evaluated vedolizumab serum trough concentrations, presence of anti-vedolizumab antibodies, and clinical outcomes over 48 weeks to assess exposure-response association and impact of thiopurine withdrawal.

Results: There were 62 UC participants with mean age of 43.4 years and 42% were females. All participants received vedolizumab as maintenance therapy with 67.7% withdrew thiopurine. Vedolizumab serum trough concentrations remained stable over 48 weeks regardless of thiopurine use, with no anti-vedolizumab antibodies detected. Patients with clinical remission had higher trough concentrations at week 48. In quartile analysis, a threshold of > 11.3 μg/mL was associated with sustained clinical remission, showing a sensitivity of 82.4%, specificity of 60.0%, and an area of receiver operating characteristic of 0.71 (95%CI: 0.49-0.93). Patients discontinuing thiopurine required higher vedolizumab concentrations for achieving remission.

Conclusion: A positive exposure-response relationship between vedolizumab trough concentrations and UC outcomes suggests that monitoring drug levels may be beneficial. While thiopurine did not influence vedolizumab levels, its withdrawal may necessitate higher vedolizumab trough concentrations to maintain remission.

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溃疡性结肠炎伴和不伴硫嘌呤的Vedolizumab血清谷浓度:前瞻性VIEWS药代动力学研究
背景:溃疡性结肠炎(UC)是一种需要持续治疗和监测的慢性炎症。维多单抗维持治疗期间的药代动力学数据有限,硫嘌呤对维多单抗浓度的影响尚不清楚。目的:探讨维多单抗的暴露-反应关系和硫嘌呤停药对维持治疗期间达到持续临床和内镜缓解的UC患者的影响。方法:这是一项前瞻性随机临床试验(VIEWS)的事后分析,该试验涉及2018年至2022年澳大利亚8个中心的UC患者。临床和内镜缓解的患者在接受维多单抗治疗的同时随机选择继续或停用硫嘌呤。我们评估了维多单抗血清谷浓度、抗维多单抗抗体的存在和48周的临床结果,以评估硫嘌呤停药的暴露-反应关联和影响。结果:62例UC患者,平均年龄43.4岁,其中42%为女性。所有参与者接受维多单抗作为维持治疗,67.7%的参与者退出硫嘌呤。无论使用硫嘌呤,Vedolizumab血清谷浓度在48周内保持稳定,未检测到抗Vedolizumab抗体。临床缓解的患者在第48周时谷浓度更高。在四分位数分析中,阈值> 11.3 μg/mL与持续临床缓解相关,敏感性为82.4%,特异性为60.0%,接受者工作特征面积为0.71 (95%CI: 0.49-0.93)。停用硫嘌呤的患者需要更高的维多单抗浓度才能达到缓解。结论:维多单抗谷底浓度与UC预后之间的正暴露-反应关系表明监测药物水平可能是有益的。虽然硫嘌呤不影响维多单抗水平,但它的停药可能需要更高的维多单抗谷浓度来维持缓解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
World Journal of Gastroenterology
World Journal of Gastroenterology 医学-胃肠肝病学
CiteScore
7.80
自引率
4.70%
发文量
464
审稿时长
2.4 months
期刊介绍: The primary aims of the WJG are to improve diagnostic, therapeutic and preventive modalities and the skills of clinicians and to guide clinical practice in gastroenterology and hepatology.
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