Department of Neurology, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
J Neurol Neurosurg Psychiatry. 2010 Dec;81(12):1374-9. doi: 10.1136/jnnp.2010.206599. Epub 2010 Jun 28.
Different preparations of intravenous immunoglobulin (IVIg) are considered to have comparable clinical efficacy but this has never been formally investigated. Some patients with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) report that some IVIg brands are more effective than others. A liquid IVIg preparation is more user friendly and potentially can be infused at a faster rate.
The primary objective was to compare the efficacy of two different IVIg brands in CIDP. The secondary objective was to compare their safety.
This was an investigator-initiated multi-centre randomised controlled double-blind trial. Twenty-seven patients with active but stable CIDP treated with their individual stable IVIg (Gammagard S/D) maintenance dose and interval were randomised to receive four infusions of freeze-dried 5% IVIg (Gammagard S/D) or the new liquid 10% IVIg (Kiovig). The overall disability sum score (ODSS) was used as the primary outcome scale. The equivalence margin was defined as a difference of ≤1 point in mean ΔODSS between treatment groups. Main secondary outcome scales were the MRC sum score and the Vigorimeter.
Repeated measurements analysis of variance, adjusted for baseline ODSS, showed a clinically insignificant treatment difference of 0.004 (95% CI -0.4 to 0.4). We also found no significant differences in any of the other outcome measures. Besides a lower occurrence of cold shivers in patients randomised to Kiovig (p=0.03), no significant differences were found in the occurrence of adverse events.
This trial demonstrated equal clinical efficacy between a freeze-dried and a liquid IVIg preparation for maintenance treatment of CIDP.
不同制剂的静脉注射免疫球蛋白(IVIg)被认为具有相当的临床疗效,但这从未得到过正式研究。一些慢性炎症性脱髓鞘性多发性神经病(CIDP)患者报告说,一些 IVIg 品牌比其他品牌更有效。液体 IVIg 制剂更便于使用,并且潜在地可以更快的速度输注。
主要目的是比较两种不同 IVIg 品牌在 CIDP 中的疗效。次要目的是比较它们的安全性。
这是一项由研究者发起的多中心随机对照双盲试验。27 例活动性但稳定的 CIDP 患者接受其个体稳定 IVIg(Gammagard S/D)维持剂量和间隔治疗,随机分为接受 4 次冻干 5%IVIg(Gammagard S/D)或新型液体 10%IVIg(Kiovig)治疗。总残疾评分(ODSS)作为主要结局量表。等效边界定义为治疗组之间平均 ΔODSS 的差异≤1 分。主要次要结局量表为 MRC 总评分和活力计。
调整基线 ODSS 的重复测量方差分析显示,治疗差异具有临床意义的 0.004(95%CI -0.4 至 0.4)。我们还发现其他任何结局指标均无显著差异。除了随机分配到 Kiovig 的患者发冷颤的发生率较低(p=0.03)外,不良事件的发生率没有显著差异。
该试验表明,在维持治疗 CIDP 方面,冻干和液体 IVIg 制剂具有同等的临床疗效。