Evidera, Bethesda, MD, USA.
Amgen Inc., Thousand Oaks, CA, USA.
Headache. 2021 Mar;61(3):438-454. doi: 10.1111/head.14053. Epub 2021 Feb 16.
Calcitonin gene-related peptide (CGRP) inhibitors were introduced in the United States (US) in 2018. To understand the changing patterns of preventive treatment following the introduction of these new agents, we must first characterize the patterns which preceded their introduction.
To characterize the burden, unmet need, and treatment patterns in patients with migraine initiating preventive migraine medications before the introduction of CGRP inhibitors in the US.
Between March 2016 and October 2017, we enrolled episodic (EM) and chronic migraine (CM) patients initiating or changing preventive treatment at primary care or neurology clinic visits in the US, in a real-world observational study using a prospective cohort design. At baseline and monthly thereafter for 6 months, we collected data from study sites and patients on migraine frequency, treatment modifications, migraine impact on functioning, and work productivity for a descriptive analysis of migraine patient experience and treatment patterns.
From the sample of 234 completers, 118 had EM (50.4%) and 116 had CM (49.6%). Mean age at enrollment was 41 years (SD = 12) and mean age at first migraine diagnosis was 22 years (SD = 11). Most participants were females (n = 204/234; 87.2%) and white (n = 178/234; 76.1%). The majority (n = 164/234; 70.1%) had not used preventive migraine treatment in the 5 years prior to enrollment (treatment naïve). At baseline, mean monthly migraine days were 9.6 days (SD = 5.0) for the preventive treatment naïve group and 12.4 days (SD = 7.0) for treatment experienced patients. The majority had severe Migraine Disability Assessment (Grade IV, total score ≥21), including 67.1% (n = 110/164) of the preventive treatment naïve and 77.1% (n = 54/70) of the preventive treatment experienced patients. Headache Impact Test total scores indicating severe impairment (score >59) occurred in 88.4% (n = 145/164) of the treatment naïve and 88.6% (n = 62/70) of treatment experienced patients. Mean work productivity loss as measured by the Work Productivity and Activity Impairment questionnaire in the subsample of employed patients was 53.3% loss. The most used acute medications at baseline were nonsteroidal anti-inflammatory agents (n = 124/234; 53.0%), acetaminophen-based products (n = 112/234; 47.9%), and triptans (n = 105/234; 44.9%). The most commonly initiated preventive treatments were topiramate (n = 100/234; 42.7%), tricyclic antidepressants (n = 39/234; 16.7%), beta-blockers (n = 26/234; 11.1%), and onabotulinumtoxinA (n = 24/234; 10.3%). Over the 6-month follow-up period, almost half of patients (n = 116/234, 49.6%) modified their preventive treatment and discontinued treatment (n = 88/312 total modifications; 28.2%) or modified their pattern of use by increasing, decreasing, or skipping doses (n = 224/312 total modifications; 71.8%), often without seeking medical advice. Avoiding side effects was the main reason reported among patients who discontinued (n = 52/88; 59.1%), decreased frequency or dose (n = 37/89; 41.6%), and skipped doses (n = 29/86; 33.7%). Perceived lack of efficacy was another frequent reason reported among those who discontinued (n = 20/88; 22.7%), decreased frequency or dose (n = 15/89; 16.9%), and skipped doses (n = 18/86; 20.9%). Despite initiation of preventive treatment and improvements observed in number of headache and migraine days, migraine patients continued to experience substantial disability, headache impact, and reduced productivity throughout the 6-month follow-up period.
Prior to 2018, the burden of migraine was high for patients initiating preventive treatments. Despite having more than 9 days of migraine per month on average, the majority (70.1%) of patients initiating prevention had been treatment naïve, indicating underuse of preventive treatments. The preventive treatments used in this study were poorly tolerated and were reported by patients to lack efficacy, resulting in suboptimal adherence. The high discontinuation rates suggest that the preventive medications being offered during the period of the study did not meet the treatment needs of patients. In addition, the decisions by about half of patients to alter their prescribed treatment plan without consulting their provider can pose substantial health risks. These findings pertain to the broad set of preventive treatments initiated in this study and do not support inferences about individual preventive treatments, due to limitations in sample size. These findings suggest the need for more effective and better tolerated preventive treatment options.
降钙素基因相关肽(CGRP)抑制剂于 2018 年在美国上市。为了了解这些新药引入后预防性治疗模式的变化,我们必须首先描述其引入前的模式。
描述美国 CGRP 抑制剂引入前偏头痛患者开始预防性偏头痛治疗的负担、未满足的需求和治疗模式。
在 2016 年 3 月至 2017 年 10 月期间,我们在初级保健或神经病学诊所就诊的偏头痛患者中招募了开始或改变预防性治疗的发作性(EM)和慢性偏头痛(CM)患者,使用前瞻性队列设计进行了一项真实世界的观察性研究。在基线和此后的 6 个月内,我们从研究地点和患者那里收集偏头痛发作频率、治疗调整、偏头痛对功能的影响以及工作生产力的信息,以描述偏头痛患者的体验和治疗模式。
从 234 名完成研究的患者中,118 名患有 EM(50.4%),116 名患有 CM(49.6%)。入组时的平均年龄为 41 岁(SD=12),首次偏头痛诊断的平均年龄为 22 岁(SD=11)。大多数参与者为女性(n=204/234;87.2%)和白人(n=178/234;76.1%)。大多数(n=164/234;70.1%)患者在入组前的 5 年内未使用预防性偏头痛治疗(治疗初治)。基线时,预防性治疗初治组的每月偏头痛发作天数为 9.6 天(SD=5.0),而治疗经验组为 12.4 天(SD=7.0)。大多数患者偏头痛残疾评估量表(Grade IV,总分≥21)严重,包括 67.1%(n=110/164)的治疗初治患者和 77.1%(n=54/70)的治疗经验患者。头痛影响测试总分表明严重损害(评分>59)的发生率在治疗初治组为 88.4%(n=145/164),在治疗经验组为 88.6%(n=62/70)。在就业患者的工作生产力和活动障碍问卷亚组中,平均工作生产力损失为 53.3%。基线时最常用的急性药物是非甾体抗炎药(n=124/234;53.0%)、对乙酰氨基酚类产品(n=112/234;47.9%)和曲坦类药物(n=105/234;44.9%)。最常开始的预防性治疗是托吡酯(n=100/234;42.7%)、三环类抗抑郁药(n=39/234;16.7%)、β受体阻滞剂(n=26/234;11.1%)和肉毒杆菌毒素 A(n=24/234;10.3%)。在 6 个月的随访期间,近一半的患者(n=116/234,49.6%)改变了他们的预防性治疗方案,并停止治疗(n=88/312 总修改数;28.2%)或通过增加、减少或跳过剂量改变了他们的用药模式(n=224/312 总修改数;71.8%),通常没有寻求医疗建议。避免副作用是停止治疗的患者(n=52/88;59.1%)、减少频率或剂量(n=37/89;41.6%)和跳过剂量(n=29/86;33.7%)报告的主要原因。报告认为治疗无效也是停止治疗的常见原因(n=20/88;22.7%)、减少频率或剂量(n=15/89;16.9%)和跳过剂量(n=18/86;20.9%)。尽管开始了预防性治疗,并且偏头痛发作的头痛和偏头痛天数有所改善,但偏头痛患者在整个 6 个月的随访期间继续经历严重的残疾、头痛影响和生产力下降。
在 2018 年之前,开始预防性治疗的偏头痛患者的负担很高。尽管平均每月有 9 天以上的偏头痛,但大多数(70.1%)开始预防的患者为治疗初治患者,这表明预防性治疗的使用率较低。本研究中使用的预防性治疗药物耐受性差,且患者报告缺乏疗效,导致依从性不佳。较高的停药率表明,在研究期间提供的预防性药物不能满足患者的治疗需求。此外,大约一半的患者决定在不咨询提供者的情况下改变他们的处方治疗计划,这可能会带来重大的健康风险。这些发现适用于本研究中开始的广泛预防性治疗方案,由于样本量的限制,不支持对个别预防性治疗方案的推断。这些发现表明需要更有效和更好耐受的预防性治疗方案。