Infliximab desensitization in patients with inflammatory bowel diseases: a safe therapeutic alternative.

IF 1.6 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Nassim Hammoudi, Déborah Hassid, Joëlle Bonnet, My-Linh Tran Minh, Clotilde Baudry, Anne Vauthier, Leila Chedouba, Pascal Houzé, Nelson Lourenco, Thomas Aparicio, Jean-Marc Gornet, Matthieu Allez
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引用次数: 0

Abstract

Background: Hypersensitivity reactions (HSR) to the administration of infliximab (IFX) in Inflammatory Bowel Diseases (IBD) patients are not rare and usually lead to drug discontinuation. We report data on safety and effectiveness of desensitization to IFX in patients with previous HSR.

Methods: We conducted a retrospective monocentric observational study. Patients for whom a desensitization protocol to IFX was realized after a previous HSR were included. Anti-drug antibodies (ADA) and IFX trough levels at both inclusion and six months after desensitization were collected. Clinical outcomes, including recurrence of HSR were evaluated.

Results: From 2005 to 2020, 27 patients (Crohn's Disease: 26 (96%) were included). Desensitization after HSR was performed after a median time of 10.4 months (2.9-33.1). Nineteen (70%) patients received immunosuppressants at time of desensitization. Eight (30%) patients presented HSR at first (n = 2), second (n = 4) or third (n = 2) IFX perfusion after desensitization. None led to intensive care unit transfer or death. Thirteen (48%) had clinical response at 6 months and 8 (29%) were still under IFX treatment two years after desensitization. IFX trough levels and ADA were available for 14 patients at time of desensitization. Most patients (12 out of 14) had ADA at a high level. At 6 months, among the 7 patients with long term response to IFX, 4 presented a decrease of ADA titers and 2 had a significant trough level of IFX.

Conclusion: IFX desensitization in patients with IBD is a safe therapeutic alternative and represents a potential option for patients refractory to multiple biologics.What is already known? Hypersensitivity reactions to the administration of infliximab is frequent. Occurrence of hypersensitivity reaction, either immediate or delayed, usually leads to permanent drug discontinuation.What is new here? Infliximab desensitization is well tolerated with no hypersensitivity reaction recurrence in 70% of patients. Clinical success at 6 months was of 48% and around a third of patients remained under infliximab therapy two years after desensitization. Antidrug antibodies decreased and infliximab trough levels increased in these patients showing the impact of desensitization on immunogenicity.How can this study help patient care? Infliximab desensitization represents a potential option for patients refractory to multiple biologics who presented hypersensitivity reaction to the drug.

炎症性肠病患者的英夫利西单抗脱敏治疗:一种安全的替代疗法。
背景:炎症性肠病(IBD)患者服用英夫利昔单抗(IFX)后出现过敏反应(HSR)并不罕见,通常会导致停药。我们报告了曾发生过 HSR 的患者对 IFX 进行脱敏治疗的安全性和有效性:我们进行了一项回顾性单中心观察研究。方法:我们进行了一项回顾性单中心观察研究。研究对象包括既往接受过 HSR 后接受过 IFX 脱敏治疗的患者。我们收集了纳入时和脱敏后六个月的抗药抗体(ADA)和 IFX 谷值水平。对包括 HSR 复发在内的临床结果进行了评估:结果:从 2005 年到 2020 年,共有 27 名患者(克罗恩病:26 人(96%)被纳入)接受了脱敏治疗:26例(96%))。HSR 后脱敏治疗的中位时间为 10.4 个月(2.9-33.1 个月)。19名(70%)患者在脱敏时服用了免疫抑制剂。8例(30%)患者在脱敏后第一次(2例)、第二次(4例)或第三次(2例)IFX灌注时出现HSR。无一例导致转入重症监护室或死亡。13例(48%)患者在6个月后出现临床反应,8例(29%)患者在脱敏治疗两年后仍在接受IFX治疗。14 名患者在脱敏时的 IFX 谷值水平和 ADA 已可查到。大多数患者(14 人中有 12 人)的 ADA 水平较高。6 个月后,在 7 名对 IFX 有长期反应的患者中,4 人的 ADA 滴度下降,2 人的 IFX 谷值显著升高:IBD患者的IFX脱敏治疗是一种安全的治疗选择,是对多种生物制剂难治的患者的一种潜在选择。使用英夫利西单抗经常出现过敏反应。发生超敏反应,无论是即刻反应还是延迟反应,通常都会导致永久停药。英夫利昔单抗脱敏治疗耐受性良好,70%的患者不会再发生超敏反应。6个月的临床成功率为48%,约三分之一的患者在脱敏治疗两年后仍在接受英夫利西单抗治疗。这些患者的抗药抗体下降,英夫利昔单抗谷值水平升高,显示了脱敏治疗对免疫原性的影响。英夫利昔单抗脱敏疗法是对多种生物制剂难治且出现药物过敏反应的患者的一种潜在选择。
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来源期刊
CiteScore
3.40
自引率
5.30%
发文量
222
审稿时长
3-8 weeks
期刊介绍: The Scandinavian Journal of Gastroenterology is one of the most important journals for international medical research in gastroenterology and hepatology with international contributors, Editorial Board, and distribution
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