Optimizing outcomes with maintenance IV UST in highly bio-exposed patients with IBD. Efficacy and adjusted regimen in real world

Alejandro Mínguez , Elena Coello , Alejandro Garrido , Paula Ripoll , María Gomez , Mariam Aguas , Marisa Iborra , Elena Cerrillo , Lluis Tortosa , Virginia Bayarri , Noemí Bueno , Maria José Fernández , Remedios Marqués , Pilar Nos , Guillermo Bastida
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Abstract

Background and aims

Ustekinumab is an effective treatment for inflammatory bowel diseases. However, some patients do not respond to conventional doses. The aim of the study was to evaluate the effectiveness of intravenous maintenance ustekinumab in patients with secondary failure.

Methods

Single-center, retrospective study in adult patients with intravenous maintenance ustekinumab. The reduction of biochemical activity markers, ustekinumab trough levels and clinical indices of activity were evaluated. Biological remission was defined as the percentage decrease fecal calprotectin ≥80% and/or final fecal calprotectin ≤250 and C reactive protein <5 mg/L.

Results

Thirty-one patients were included: Crohn's disease 77.4%. All included patients were bio-exposed and 61.3% had carried ≥2 biologics.
Pre-intravenous maintenance mean Harvey–Bradshaw Index was 6.5 ± 4.38 vs 5 ± 3.1 at week 8 (p = 0.024) vs 4.1 ± 3.1 at week 24 (p = 0.019). The median ustekinumab trough level pre-intravenous maintenance was 1.40 μg/ml [IQR 2.3] vs 5.35 μg/ml [IQR 4.1] at week 8 (p < 0.001) vs 4.8 μg/ml [IQR 3.9] at week 24 (p < 0.001). The pre-intravenous maintenance median fecal calprotectin was 809 μg/g [IQR: 2256] vs 423 μg/g [IQR: 999] at week 8 (p = 0.025) vs 333 μg/g [508] (p = 0.001) at week 24.
At the end of follow-up 48% went into biological remission. The presence of perianal disease was associated with lower biological remission (70.6% vs 27.3%, p = 0.025). Median intravenous ustekinumab maintenance time was 8.55 [IQR 23.9] months. In 83.9% of patients no serious infections or malignancy were documented.

Conclusions

The use of maintenance intravenous ustekinumab appears to be an effective and safe strategy that can be evaluated as a salvage treatment especially in highly bio-exposed patients.
高度生物暴露的IBD患者维持静脉UST的优化结果现实世界的疗效和调整方案
背景和目的sustekinumab是治疗炎症性肠病的有效药物。然而,一些患者对常规剂量没有反应。该研究的目的是评估静脉内维持ustekinumab在继发性衰竭患者中的有效性。方法采用单中心、回顾性研究,对静脉使用ustekinumab维持治疗的成人患者进行研究。评估生化活性标志物的降低、ustekinumab谷水平和临床活性指标。生物缓解定义为粪钙保护蛋白下降百分比≥80%和/或最终粪钙保护蛋白≤250和C反应蛋白≤5mg /L。结果纳入31例患者:克罗恩病77.4%。所有纳入的患者均有生物暴露,61.3%的患者携带≥2种生物制剂。静脉维持前平均Harvey-Bradshaw指数分别为6.5±4.38和5±3.1 (p = 0.024)和4.1±3.1 (p = 0.019)。第8周时,ustekinumab静脉前维持中位水平为1.40 μg/ml [IQR 2.3] vs 5.35 μg/ml [IQR 4.1] (p <;0.001) vs第24周4.8 μg/ml [IQR 3.9] (p <;0.001)。静脉前维持粪钙保护蛋白中位数为809 μg/g [IQR: 2256],第8周为423 μg/g [IQR: 999] (p = 0.025),第24周为333 μg/g [508] (p = 0.001)。在随访结束时,48%的患者进入生物缓解期。肛周疾病的存在与较低的生物学缓解相关(70.6% vs 27.3%, p = 0.025)。中位静脉ustekinumab维持时间为8.55 [IQR 23.9]个月。83.9%的患者无严重感染或恶性肿瘤。结论静脉使用维持性ustekinumab似乎是一种有效和安全的策略,可以作为一种补救性治疗进行评估,特别是在高度生物暴露的患者中。
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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