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视神经脊髓炎谱系疾病一线免疫抑制治疗反应的预测因素。

Predictors of response to first-line immunosuppressive therapy in neuromyelitis optica spectrum disorders.

机构信息

Department of Neurology, Research Institute and Hospital of National Cancer Center, Goyang-si, Korea.

Biometric Research Branch, Research Institute and Hospital of National Cancer Center, Goyang-si, Korea.

出版信息

Mult Scler. 2017 Dec;23(14):1902-1908. doi: 10.1177/1352458516687403. Epub 2017 Jan 12.

Abstract

BACKGROUND

Azathioprine (AZA) and mycophenolate mofetil (MMF) are the most commonly used first-line therapies for patients with neuromyelitis optica spectrum disorders (NMOSD). However, some patients experience a relapse following AZA or MMF treatment.

OBJECTIVES

To identify factors that predict a response to AZA or MMF in NMOSD.

METHODS

We retrospectively evaluated medical records from 116 patients who were initially treated with AZA or MMF for at least 6 months. Poor response was defined as ⩾2 relapses or ⩾1 severe relapse.

RESULTS

Among the 116 patients, 40 (34%) were classified as poor responders. Logistic regression analyses revealed that a poor response was independently associated with a pre-treatment history of a severe attack ( p < 0.001) and a younger age at disease onset ( p = 0.022). Among the 40 patients with a poor response, 29 (73%) switched to rituximab, and only 3 (10%) had a poor response to rituximab.

CONCLUSION

Patients with a pre-treatment history of a severe attack and a younger age of onset exhibited an increased risk of a poor response to AZA or MMF therapy. Identifying patients who are unlikely to respond to AZA or MMF therapy may allow for treatment with more potent therapies that improve treatment outcomes.

摘要

背景

硫唑嘌呤(AZA)和吗替麦考酚酯(MMF)是视神经脊髓炎谱系疾病(NMOSD)患者最常用的一线治疗药物。然而,一些患者在 AZA 或 MMF 治疗后会复发。

目的

确定预测 NMOSD 患者对 AZA 或 MMF 反应的因素。

方法

我们回顾性评估了 116 例至少接受 AZA 或 MMF 治疗 6 个月以上的患者的病历。不良反应定义为≥2 次复发或≥1 次严重复发。

结果

在 116 例患者中,40 例(34%)被归类为不良反应者。逻辑回归分析显示,不良反应与治疗前有严重发作史(p<0.001)和发病年龄较小(p=0.022)独立相关。在 40 例不良反应患者中,29 例(73%)转为利妥昔单抗治疗,仅有 3 例(10%)对利妥昔单抗治疗反应不佳。

结论

有治疗前严重发作史和发病年龄较小的患者对 AZA 或 MMF 治疗的不良反应风险增加。识别对 AZA 或 MMF 治疗反应不佳的患者可能有助于使用更有效的治疗方法改善治疗结局。

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