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对原研那他珠单抗和生物类似药那他珠单抗的JC病毒检测性能进行比较。

A comparison of JC virus assay performance provided with originator and biosimilar natalizumab.

作者信息

Varley James, Beyrouti Rahma, Nicholas Richard, Dorsey Rachel, Brownlee Wallace, Paling David, Mathews Joela, Dobson Ruth

机构信息

Department of Neurology, Imperial College Healthcare NHS Trust, London, UK.

Queen Square Multiple Sclerosis Centre, Department of Neuroinflammation, UCL Institute of Neurology, London, UK.

出版信息

Mult Scler. 2025 Jun;31(7):882-885. doi: 10.1177/13524585251346652. Epub 2025 Jun 14.

Abstract

BACKGROUND

A rare complication of natalizumab treatment is progressive multifocal leukoencephalopathy (PML); risk can be stratified using JC virus (JCV) antibody status. Risk calculators to aid clinical decision-making use cohort data tested using the Stratify-JCV assay. Following concerns of an increased number of JCV seropositive results following the switch to biosimilar natalizumab and the associated test switch, we sought to understand the clinical implications.

METHODS

A total of 497 people with MS, who had switched from Tysabri to Tyruko with sequential results available on both assays, were included.

RESULTS

Of 250 patients negative on Stratify-JCV, 119 (47.6%) were subsequently positive on ImmunoWELL. Agreement was the poorest at lower JCV index, where positive/negative cutoffs inform risk stratification and pharmacovigilance protocols most significantly.

CONCLUSION

These observed differences create uncertainty in how to counsel patients and best carry out PML surveillance. Specific concerns include overestimating risk leading to increased patient concern, increased monitoring burden and associated healthcare costs and lack of access to a highly effective therapy. It is incumbent on all stakeholders including pharmaceutical industry and test developers, patient groups, governmental authorities (including regulatory bodies) and clinicians to work together to find an expeditious solution.

摘要

背景

那他珠单抗治疗的一种罕见并发症是进行性多灶性白质脑病(PML);可使用JC病毒(JCV)抗体状态对风险进行分层。用于辅助临床决策的风险计算器使用经Stratify-JCV检测法检验的队列数据。在有人担心改用生物类似物那他珠单抗后JCV血清学阳性结果数量增加以及相关检测方法改变之后,我们试图了解其临床意义。

方法

纳入了总共497例从泰萨比(Tysabri)改用替鲁科(Tyruko)且两种检测方法均有连续结果的多发性硬化症患者。

结果

在Stratify-JCV检测为阴性的250例患者中,119例(47.6%)随后在ImmunoWELL检测中呈阳性。在较低的JCV指数时一致性最差,而阳性/阴性临界值对风险分层和药物警戒方案的影响最为显著。

结论

这些观察到的差异给如何向患者提供咨询以及如何最好地开展PML监测带来了不确定性。具体问题包括高估风险导致患者担忧增加、监测负担加重以及相关医疗成本增加,以及无法获得高效治疗。制药行业、检测开发商、患者团体、政府当局(包括监管机构)和临床医生等所有利益相关方有责任共同努力,找到快速解决办法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c05/12171048/69055c5f6499/10.1177_13524585251346652-fig1.jpg

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