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依库珠单抗改善难治性全身型重症肌无力的疲劳症状。

Eculizumab improves fatigue in refractory generalized myasthenia gravis.

机构信息

Department of Neurology, Aarhus University Hospital, Indgang J, Plan 5, Krydspunkt 504, Palle Juul-Jensens Boulevard, 8200, Aarhus N, Denmark.

Foundation of the Carlo Besta Neurological Institute, IRCCS, Milan, Italy.

出版信息

Qual Life Res. 2019 Aug;28(8):2247-2254. doi: 10.1007/s11136-019-02148-2. Epub 2019 Mar 23.

Abstract

PURPOSE

To evaluate the effect of eculizumab on perceived fatigue in patients with anti-acetylcholine receptor antibody-positive, refractory, generalized myasthenia gravis (MG) using the Quality of Life in Neurological Disorders (Neuro-QOL) Fatigue subscale, and to evaluate correlations between improvements in Neuro-QOL Fatigue and other clinical endpoints.

METHODS

Neuro-QOL Fatigue, MG Activities of Daily Living (MG-ADL), Quantitative MG (QMG), and the 15-item MG Quality of Life (MG-QOL15) scales were administered during the phase 3, randomized, placebo-controlled REGAIN study (eculizumab, n = 62; placebo, n = 63) and subsequent open-label extension (OLE). Data were analyzed using repeated-measures models. Correlations between changes in Neuro-QOL Fatigue and in MG-ADL, QMG, and MG-QOL15 scores were determined at REGAIN week 26.

RESULTS

At REGAIN week 26, eculizumab-treated patients showed significantly greater improvements in Neuro-QOL Fatigue scores than placebo-treated patients (consistent with improvements in MG-ADL, QMG, and MG-QOL15 scores previously reported in REGAIN). Improvements with eculizumab were sustained through OLE week 52. Correlations between Neuro-QOL Fatigue and MG-QOL15, MG-ADL, and QMG scores were strong for eculizumab-treated patients at REGAIN week 26, and strong, moderate, and weak, respectively, for placebo-treated patients.

CONCLUSIONS

Compared with placebo, eculizumab was associated with improvements in perceived fatigue that strongly correlated with improvements in MG-specific outcome measures. Trial ID Registration: NCT01997229, NCT02301624.

摘要

目的

使用生活质量在神经疾病(Neuro-QOL)疲劳量表评估依库珠单抗对乙酰胆碱受体抗体阳性、难治性、全身性重症肌无力(MG)患者感知疲劳的影响,并评估Neuro-QOL 疲劳改善与其他临床终点之间的相关性。

方法

在 3 期、随机、安慰剂对照的 REGAIN 研究(依库珠单抗,n=62;安慰剂,n=63)和随后的开放标签扩展(OLE)期间,使用神经 QOL 疲劳、MG 日常生活活动量表(MG-ADL)、定量 MG(QMG)和 15 项 MG 生活质量量表(MG-QOL15)进行评估。使用重复测量模型进行数据分析。在 REGAIN 第 26 周,确定了 Neuro-QOL 疲劳和 MG-ADL、QMG 和 MG-QOL15 评分变化之间的相关性。

结果

在 REGAIN 第 26 周,依库珠单抗治疗患者的 Neuro-QOL 疲劳评分改善明显优于安慰剂治疗患者(与之前在 REGAIN 中报告的 MG-ADL、QMG 和 MG-QOL15 评分改善一致)。通过 OLE 第 52 周,依库珠单抗的改善仍在持续。在 REGAIN 第 26 周,依库珠单抗治疗患者的 Neuro-QOL 疲劳评分与 MG-QOL15、MG-ADL 和 QMG 评分之间的相关性较强,而安慰剂治疗患者的相关性则分别为较强、中度和弱。

结论

与安慰剂相比,依库珠单抗治疗与感知疲劳的改善相关,与 MG 特定结局测量的改善具有很强的相关性。试验注册号:NCT01997229,NCT02301624。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2fd/6620379/35a518dc9e1d/11136_2019_2148_Fig1_HTML.jpg

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