Endocrine and multiple sclerosis outcomes in patients with autoimmune thyroid events in the alemtuzumab CARE-MS studies.

IF 2.5 Q2 CLINICAL NEUROLOGY
Colin M Dayan, Beatriz Lecumberri, Ilaria Muller, Sashiananthan Ganesananthan, Samuel F Hunter, Krzysztof W Selmaj, Hans-Peter Hartung, Eva K Havrdova, Christopher C LaGanke, Tjalf Ziemssen, Bart Van Wijmeersch, Sven G Meuth, David H Margolin, Elizabeth M Poole, Darren P Baker, Peter A Senior
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引用次数: 1

Abstract

Background: Alemtuzumab is an effective therapy for relapsing multiple sclerosis. Autoimmune thyroid events are a common adverse event.

Objective: Describe endocrine and multiple sclerosis outcomes over 6 years for alemtuzumab-treated relapsing multiple sclerosis patients in the phase 3 CARE-MS I, II, and extension studies who experienced adverse thyroid events.

Methods: Endocrine and multiple sclerosis outcomes were evaluated over 6 years. Thyroid event cases, excluding those pre-existing or occurring after Year 6, were adjudicated retrospectively by expert endocrinologists independently of the sponsor and investigators.

Results: Thyroid events were reported for 378/811 (46.6%) alemtuzumab-treated patients. Following adjudication, endocrinologists reached consensus on 286 cases (75.7%). Of these, 39.5% were adjudicated to Graves' disease, 2.5% Hashimoto's disease switching to hyperthyroidism, 15.4% Hashimoto's disease, 4.9% Graves' disease switching to hypothyroidism, 10.1% transient thyroiditis, and 27.6% with uncertain diagnosis; inclusion of anti-thyroid antibody status reduced the number of uncertain diagnoses. Multiple sclerosis outcomes of those with and without thyroid events were similar.

Conclusion: Adjudicated thyroid events occurring over 6 years for alemtuzumab-treated relapsing multiple sclerosis patients were primarily autoimmune. Thyroid events were considered manageable and did not affect disease course. Thyroid autoimmunity is a common but manageable adverse event in alemtuzumab-treated relapsing multiple sclerosis patients.ClinicalTrials.gov Registration Numbers: CARE-MS I (NCT00530348); CARE-MS II (NCT00548405); CARE-MS Extension (NCT00930553).

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阿仑单抗CARE-MS研究中自身免疫性甲状腺事件患者的内分泌和多发性硬化症结局
背景:阿仑单抗是治疗复发性多发性硬化症的有效药物。自身免疫性甲状腺事件是一种常见的不良事件。目的:描述在CARE-MS I、II期和扩展研究中,阿仑单抗治疗的复发性多发性硬化症患者6年以上的内分泌和多发性硬化症结局,这些患者经历了甲状腺不良事件。方法:6年内评估内分泌和多发性硬化症的预后。甲状腺事件病例,排除那些已经存在或在6年后发生的病例,由独立于发起人和研究人员的内分泌专家回顾性裁决。结果:378/811例(46.6%)阿仑单抗治疗患者报告了甲状腺事件。经裁定,内分泌科医师意见一致286例(75.7%)。其中,39.5%确诊为格雷夫斯病,2.5%为桥本病,15.4%为桥本病,4.9%为格雷夫斯病,10.1%为短暂性甲状腺炎,27.6%诊断不明确;纳入抗甲状腺抗体状态减少了不确定诊断的数量。有和没有甲状腺事件的多发性硬化症结果相似。结论:阿仑单抗治疗的复发性多发性硬化症患者6年内发生的甲状腺事件主要是自身免疫性的。甲状腺事件被认为是可控的,不影响病程。在阿仑单抗治疗的复发性多发性硬化症患者中,甲状腺自身免疫是一种常见但可控的不良事件。Care-ms ii (nct00548405);CARE-MS扩展(NCT00930553)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.70
自引率
0.00%
发文量
54
审稿时长
15 weeks
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