Comparative effectiveness of erenumab versus rimegepant for migraine prevention using matching-adjusted indirect comparison.

IF 1.9 4区 医学 Q3 HEALTH CARE SCIENCES & SERVICES Journal of comparative effectiveness research Pub Date : 2024-03-01 Epub Date: 2024-01-04 DOI:10.57264/cer-2023-0122
Ronan Mahon, Santosh Tiwari, Mirja Koch, Matias Ferraris, Keith A Betts, Yan Wang, Sophie Gao, Pascal Proot
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Abstract

Aim: To compare the efficacy of erenumab versus rimegepant as preventive treatment for patients with episodic and chronic migraine using an anchor-based matching-adjusted indirect comparison. Methods: Patients from two phase II/III trials for erenumab (NCT02066415 and NCT02456740) were pooled and weighted to match on the baseline effect modifiers (age, sex, race, baseline monthly migraine days [MMDs], and history of chronic migraine [CM]) reported in the phase II/III trial for rimegepant (NCT03732638). Four efficacy outcomes were compared between the two erenumab regimens (70 mg and 140 mg) and rimegepant, including changes in MMDs from baseline to month 1 and month 3, changes in Migraine-Specific Quality of Life Questionnaire role function - restrictive domain score from baseline to month 3, and change in disability from baseline to Month 3. Results: Compared with rimegepant, erenumab 70 mg was associated with a statistically significant reduction in MMDs at month 3 (-0.90 [-1.76, -0.03]; p = 0.042) and erenumab 140 mg was associated with statistically significant reductions in MMDs at month 1 (-0.94 [-1.70, -0.19]; p = 0.014) and month 3 (-1.28 [-2.17, -0.40]; p = 0.005). The erenumab regimens also had numerical advantages over rimegepant for other efficacy outcomes. Conclusion: In the present study, we found that erenumab had a more favorable efficacy profile than rimegepant in reducing MMDs at month 1 and month 3 for migraine prevention. These results may help with decision-making in clinical practice and can be further validated in future clinical trials or real-world studies.

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使用匹配调整间接比较法比较艾伦单抗与利美康在预防偏头痛方面的疗效。
目的:采用基于锚匹配调整的间接比较法,比较艾伦单抗与利美昔班作为发作性和慢性偏头痛患者预防性治疗的疗效。研究方法对来自两项艾伦单抗II/III期试验(NCT02066415和NCT02456740)的患者进行汇总和加权,以匹配利美喷剂II/III期试验(NCT03732638)中报告的基线效应修饰因子(年龄、性别、种族、基线每月偏头痛天数[MMDs]和慢性偏头痛病史[CM])。研究人员比较了两种艾伦单抗治疗方案(70 毫克和 140 毫克)和利美昔单抗的四项疗效结果,包括从基线到第 1 个月和第 3 个月偏头痛天数的变化、从基线到第 3 个月偏头痛特定生活质量问卷角色功能-限制性领域得分的变化,以及从基线到第 3 个月残疾程度的变化:与利美康相比,艾伦单抗 70 毫克可在第 3 个月显著减少偏头痛症状(-0.90 [-1.76, -0.03];p = 0.042),艾伦单抗 140 毫克可在第 1 个月显著减少偏头痛症状(-0.94 [-1.70, -0.19];p = 0.014),第 3 个月显著减少偏头痛症状(-1.28 [-2.17, -0.40];p = 0.005)。在其他疗效结果方面,艾伦单抗方案也比利美昔班方案具有数字优势。结论在本研究中,我们发现在预防偏头痛方面,艾伦单抗在第1个月和第3个月减少MMD方面的疗效优于利美昔班。这些结果可能有助于临床实践中的决策,并可在未来的临床试验或实际研究中得到进一步验证。
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来源期刊
Journal of comparative effectiveness research
Journal of comparative effectiveness research HEALTH CARE SCIENCES & SERVICES-
CiteScore
3.50
自引率
9.50%
发文量
121
期刊介绍: Journal of Comparative Effectiveness Research provides a rapid-publication platform for debate, and for the presentation of new findings and research methodologies. Through rigorous evaluation and comprehensive coverage, the Journal of Comparative Effectiveness Research provides stakeholders (including patients, clinicians, healthcare purchasers, and health policy makers) with the key data and opinions to make informed and specific decisions on clinical practice.
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