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评估多发性硬化症患者从那他珠单抗转换为奥瑞珠单抗的疗效和安全性(OCTAVE研究)。

Evaluating the efficacy and safety of transitioning patients with multiple sclerosis from natalizumab to ocrelizumab (OCTAVE).

作者信息

Smoot Kyle, Marginean Horia, Gervasi-Follmar Tiffany, Chen Chiayi, Repovic Pavle, Cohan Stanley

机构信息

Providence Brain and Spine Institute, Portland, OR, USA.

Multiple Sclerosis Center, Swedish Neuroscience Institute, Seattle, WA, USA.

出版信息

Mult Scler. 2023 Jul;29(8):956-966. doi: 10.1177/13524585231175284. Epub 2023 Jun 15.

Abstract

INTRODUCTION

Natalizumab is associated with a risk of progressive multifocal leukoencephalopathy (PML) in multiple sclerosis (MS) patients infected with John Cunningham virus (JCV). Ocrelizumab has demonstrated efficacy to treat MS; however, its safety in patients previously treated with natalizumab is unclear.

OBJECTIVE

To evaluate the safety and efficacy of ocrelizumab in patients with relapsing MS (RMS) previously treated with natalizumab.

METHODS

Clinically and radiographically stable RMS patients, ages 18-65 treated with natalizumab for ⩾ 12 months, were enrolled in the study and initiated ocrelizumab 4-6 weeks after their final dose of natalizumab. Relapse assessment, expanded disability status scale, and brain magnetic resonance imaging (MRI) were performed prior to starting ocrelizumab and at months 3, 6, 9, and 12.

RESULTS

Forty-three patients were enrolled, and 41 (95%) completed the study. Two patients had a relapse while on ocrelizumab, one at month 9 and the other at month 12, without changes on brain MRI. Two additional patients had new brain MRI lesions detected at month 3, with no new symptoms. Thirteen serious adverse events (SAEs) were recorded, four of which were considered possibly related to ocrelizumab.

CONCLUSION

Overall, our study indicates clinical and MRI stability for most patients transitioning from natalizumab to ocrelizumab.

CLINICALTRIALS.GOV IDENTIFIER: NCT03157830.

摘要

引言

那他珠单抗与感染约翰·坎宁安病毒(JCV)的多发性硬化症(MS)患者发生进行性多灶性白质脑病(PML)的风险相关。奥瑞珠单抗已证明对治疗MS有效;然而,其在先前接受那他珠单抗治疗的患者中的安全性尚不清楚。

目的

评估奥瑞珠单抗在先前接受那他珠单抗治疗的复发型MS(RMS)患者中的安全性和有效性。

方法

纳入年龄在18 - 65岁、接受那他珠单抗治疗≥12个月且临床和影像学稳定的RMS患者,在最后一剂那他珠单抗后4 - 6周开始使用奥瑞珠单抗。在开始使用奥瑞珠单抗之前以及第3、6、9和12个月进行复发评估、扩展残疾状态量表评估和脑磁共振成像(MRI)检查。

结果

43名患者入组,41名(95%)完成研究。两名患者在使用奥瑞珠单抗期间复发,一名在第9个月,另一名在第12个月,脑MRI无变化。另外两名患者在第3个月检测到新的脑MRI病变,无新症状。记录了13起严重不良事件(SAE),其中4起被认为可能与奥瑞珠单抗有关。

结论

总体而言,我们的研究表明,大多数从那他珠单抗过渡到奥瑞珠单抗的患者在临床和MRI方面保持稳定。

临床试验注册号

NCT03157830

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