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醋酸格拉替雷 40mg 注射后迟发性非典型反应:需要滴定吗?

Atypical Post-Injection Reactions with Delayed Onset Following Glatiramer Acetate 40 mg: Need for Titration?

机构信息

Neurocenter of Southern Switzerland, Ospedale Regionale di Lugano, Lugano, Switzerland.

Neuroimmunology and Neuromuscular Diseases Unit, IRCCS Fondazione Istituto Neurologico Carlo Besta, Milan, Italy.

出版信息

CNS Drugs. 2018 Jul;32(7):653-660. doi: 10.1007/s40263-018-0529-1.

Abstract

BACKGROUND

Glatiramer acetate (GA) 20 mg/day (GA20) is associated with immediate post-injection reactions (PIRs). For convenience of use, approved GA 40 mg three times weekly (GA40) delivers a similar weekly dose. The dose and concentration of a single GA40 injection are, however, twice as high as for GA20, and post-injection adverse events may differ. Cases of atypical PIRs to GA40 prompted us to systematically monitor such events.

OBJECTIVE

The aim was to characterize atypical PIRs in multiple sclerosis (MS) patients treated with GA40.

METHODS

Clinical practice data were prospectively collected in consecutive relapsing-remitting MS patients. Descriptive statistics for categorical and continuous variables, Mann-Whitney and Chi-squared tests for baseline comparisons, and Cox regression models for association of variables to first atypical PIRs were applied.

RESULTS

Forty-six out of 173 patients (26.6%) given GA40 experienced any PIRs. Of those, 38 (22.0%) had atypical, 14 (8.1%) had combined typical and atypical, and 26 (15.0%) had recurrent atypical PIRs, most frequently shivering (13.3%) and nausea/vomiting (8.1%). Compared to typical PIRs, onset of atypical PIRs was significantly delayed (median 30 vs 1 min, p < 0.0001), and their median duration longer (median 120 vs 6 min, p = 0.00013). Previous exposure to GA20 was associated with a lower risk of atypical PIRs [hazard ratio (HR) = 0.35, 95% confidence interval (CI) 0.17-0.72, p = 0.0039]. Patients experiencing PIRs with GA20 were at elevated risk for atypical PIRs with GA40 (HR = 5.75, 95% CI 1.66-19.94, p = 0.0059).

CONCLUSIONS

Atypical PIRs with GA40, especially gastrointestinal symptoms and/or fever/shivering, had a delayed onset and occurred in a significant proportion of our patients. Their real prevalence should be assessed in appropriately designed studies accounting for  nocebo responses. Initial dose titration might reduce PIR frequency.

摘要

背景

每天 20 毫克(GA20)的醋酸格拉替雷与注射后即刻反应(PIR)有关。为了使用方便,批准的每周三次 40 毫克(GA40)可提供相似的每周剂量。然而,单次 GA40 注射的剂量和浓度是 GA20 的两倍,注射后的不良反应可能不同。由于 GA40 出现了非典型 PIR 病例,我们开始系统地监测此类事件。

目的

本研究旨在描述接受 GA40 治疗的多发性硬化症(MS)患者的非典型 PIR。

方法

连续入组复发性缓解型 MS 患者,前瞻性收集临床实践数据。对分类和连续变量进行描述性统计,对基线比较进行曼-惠特尼和卡方检验,对首次出现非典型 PIR 的变量进行 Cox 回归模型分析。

结果

在 173 名接受 GA40 治疗的患者中,有 46 名(26.6%)出现任何 PIR。其中,38 名(22.0%)出现非典型 PIR,14 名(8.1%)出现典型和非典型混合 PIR,26 名(15.0%)出现复发性非典型 PIR,最常见的是颤抖(13.3%)和恶心/呕吐(8.1%)。与典型 PIR 相比,非典型 PIR 的发病时间明显延迟(中位数 30 分钟 vs 1 分钟,p<0.0001),持续时间较长(中位数 120 分钟 vs 6 分钟,p=0.00013)。先前接触 GA20 与非典型 PIR 风险降低相关[风险比(HR)=0.35,95%置信区间(CI)0.17-0.72,p=0.0039]。接受 GA20 治疗出现 PIR 的患者,发生 GA40 非典型 PIR 的风险升高(HR=5.75,95%CI 1.66-19.94,p=0.0059)。

结论

GA40 引起的非典型 PIR,特别是胃肠道症状和/或发热/颤抖,发病时间较晚,在我们的患者中占很大比例。在适当设计的研究中,应考虑到安慰剂效应,评估其真实患病率。初始剂量滴定可能会降低 PIR 的发生频率。

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