治疗药物监测和中和抗药物抗体检测优化tnf - α抑制剂治疗葡萄膜炎。

Frontiers in ophthalmology Pub Date : 2025-01-28 eCollection Date: 2025-01-01 DOI:10.3389/fopht.2025.1432935
Howard C Chen, Jenny Shunyakova, Amit K Reddy, Srujay Pandiri, Lynn Hassman
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引用次数: 0

摘要

背景:每隔一周服用阿达木单抗是治疗慢性难治性葡萄膜炎的有效方法。对这种治疗反应不佳的患者可能会出现复发性炎症和视力丧失。在这里,我们研究了使用治疗药物监测和中和抗药物抗体检测作为优化对阿达木单抗初始剂量反应不理想的患者的肿瘤坏死因子(TNF)- α抑制剂治疗的策略。方法:2015年至2023年在美国两家三级转诊葡萄膜炎服务机构进行回顾性队列研究。非感染性葡萄膜炎患者对每两周剂量的阿达木单抗反应不佳,并接受血清阿达木单抗水平和抗药物抗体检测。当血清药物水平较低(小于或等于6微克/毫升)且反射试验中存在抗阿达木单抗抗体时,患者被认为具有中和性药物抗体。临床医生根据血清阿达木单抗水平和存在或不存在中和药物抗体的情况进行治疗调整。基于这些发现,每两周给药的阿达木单抗要么升级到每周给药,要么切换到英夫利昔单抗,一种替代的tnf - α抑制剂。主要结局是12个月时的成功或失败,由保留类固醇治疗的疾病不活动决定。结果:包括32例对阿达木单抗初始剂量反应不理想的患者。31.2% (n=10)的患者存在中和性药物抗体。所有具有中和性药物抗体的患者在12个月时将药物转换为英夫利昔单抗,缓解率为40%。没有中和药物抗体的患者(n=22)接受剂量递增(77.3%;17例)或药物切换(22.7%;N =5), 12个月的缓解率为68.2%。总之,在我们的队列中,基于治疗药物监测和中和药物抗体检测的治疗调整导致缓解率为62.5%。结论:对于每两周给药一次阿达木单抗治疗反应不理想的葡萄膜炎患者,治疗药物监测和中和药物抗体检测可能有助于临床医生优化tnf - α抑制剂的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapeutic drug monitoring and neutralizing anti-drug antibody detection to optimize TNF-alpha inhibitor treatment for uveitis.

Background: Adalimumab taken every other week is an effective treatment in patients with chronic refractory uveitis. Patients who have a suboptimal response to this treatment may suffer from recurrent inflammation and vision loss. Here, we investigated the use of therapeutic drug monitoring and neutralizing anti-drug antibody detection as a strategy to optimize tumor necrosis factor (TNF)-alpha inhibitor treatment in patients who have a suboptimal response to the initial dosing of adalimumab.

Method: Retrospective cohort study performed in two tertiary referral uveitis services in the United States between 2015 to 2023. Patients with non-infectious uveitis who had a suboptimal response to every two-week dosing of adalimumab and underwent serum adalimumab level with reflex to anti-drug antibody testing were followed. Patients were considered to have neutralizing drug antibodies when serum drug levels were low (less than or equal to 6 mcg/mL) and anti-adalimumab antibodies were present on reflex testing. Treatment adjustment was made by clinicians with the knowledge of serum adalimumab level and the presence or absence of neutralizing drug antibodies. Every two-week dosing of adalimumab was either escalated to weekly dosing or switched to infliximab, an alternate TNF-alpha inhibitor, based on these findings. The primary outcome was success or failure at 12 months, as determined by disease inactivity on steroid-sparing therapy.

Results: 32 patients with suboptimal response to the initial dosing of adalimumab were included. 31.2% (n=10) of patients were found to have neutralizing drug antibodies. All patients with neutralizing drug antibodies underwent a medication switch to infliximab with a remission rate of 40% at 12 months. Patients without neutralizing drug antibodies (n=22) underwent dose escalation (77.3%; n=17) or medication switch (22.7%; n=5) and achieved a remission rate of 68.2% at 12 months. Altogether, treatment adjustment based on therapeutic drug monitoring and neutralizing drug antibody detection, in our cohort, resulted in a remission rate of 62.5%.

Conclusions: For patients with uveitis experiencing suboptimal therapeutic response to adalimumab dosed every two weeks, therapeutic drug monitoring and neutralizing drug antibody detection may help clinicians optimize TNF-alpha inhibitor treatment.

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