Lilly Research Laboratories, Lilly Corporate Center, Indianapolis, IN, USA.
Center for Headache Care and Research, Island Neurological Associates, a division of ProHEALTHcare Associates, Plainview, NY, USA.
J Headache Pain. 2020 Jun 23;21(1):79. doi: 10.1186/s10194-020-01148-9.
Migraine clinical profile may change with age, making it necessary to verify that migraine treatments are equally safe and effective in older patients. These analyses evaluated the effects of patient age on the pharmacokinetics (PK), efficacy, and safety of galcanezumab for prevention of migraine.
Analyses included efficacy data from three double-blind phase 3 clinical trials: two 6-month studies in episodic migraine (EVOLVE-1, EVOLVE-2: N = 1773) and one 3-month study in chronic migraine (REGAIN:N = 1113). Patients were randomized 2:1:1 to placebo, galcanezumab 120 mg, or galcanezumab 240 mg. Safety and PK data included additional phase 2 and phase 3 trials for a larger sample size of patients > 60 years (range = 18-65 for all studies). Subgroup analyses assessed efficacy measures, adverse event (AE) occurrence, and cardiovascular measurement changes by patient age group. Galcanezumab PK were evaluated using a population analysis approach, where age was examined as a potential covariate on apparent clearance (CL/F) and apparent volume of distribution (V/F) of galcanezumab.
Numbers of baseline monthly migraine headache days were similar across age groups. There were no statistically significant treatment-by-age group interactions for any efficacy measures, except in episodic migraine studies where older patients appeared to have a larger reduction than younger patients in the number of monthly migraine headache days with acute medication use. Age (18-65) had a minimal effect on CL/F, and no effect on V/F. Galcanezumab-treated patients ≥60 years experienced no clinically meaningful increases in blood pressure and no increased frequency in treatment-emergent AEs, discontinuations due to AEs, serious adverse events (SAEs) overall, or cardiovascular SAEs, compared to age-matched placebo-treated patients.
Age (up to 65 years) does not affect efficacy in migraine prevention and has no clinically meaningful influence on galcanezumab PK to warrant dose adjustment. Furthermore, older galcanezumab-treated patients experienced no increases in frequency of AEs or increases in blood pressure compared with age-matched placebo-treated patients.
EVOLVE-1 (NCT02614183, registered 23 November 2015), EVOLVE-2 (NCT02614196, 23 November 2015), REGAIN (NCT02614261, 23 November 2015), ART-01 (NCT01625988, 20 June 2012, ), I5Q-MC-CGAB (NCT02163993, 12 June 2014, ), I5Q-MC-CGAJ (NCT02614287, 23 November 2015, ), all retrospectively registered.
偏头痛的临床特征可能会随年龄变化,因此有必要验证偏头痛的治疗方法在老年患者中同样安全有效。这些分析评估了患者年龄对加奈珠单抗预防偏头痛的药代动力学(PK)、疗效和安全性的影响。
分析包括三项双盲 3 期临床试验的疗效数据:两项发作性偏头痛的 6 个月研究(EVOLVE-1、EVOLVE-2:N=1773)和一项慢性偏头痛的 3 个月研究(REGAIN:N=1113)。患者按 2:1:1 的比例随机分配至安慰剂、加奈珠单抗 120mg 或加奈珠单抗 240mg 组。安全性和 PK 数据包括更大样本量(所有研究的年龄范围为 18-65 岁)的额外 2 期和 3 期试验。亚组分析按患者年龄组评估疗效指标、不良事件(AE)发生情况和心血管测量变化。采用群体分析方法评估加奈珠单抗 PK,其中年龄被视为加奈珠单抗表观清除率(CL/F)和表观分布容积(V/F)的潜在协变量。
各年龄组基线每月偏头痛头痛天数相似。除在发作性偏头痛研究中,年龄与治疗组之间无统计学意义的交互作用外,对于任何疗效指标,各年龄组间均无统计学意义的治疗与年龄组交互作用,除在发作性偏头痛研究中,老年患者与年轻患者相比,急性药物治疗后每月偏头痛头痛天数减少更多。年龄(18-65 岁)对 CL/F 的影响极小,对 V/F 无影响。与年龄匹配的安慰剂治疗患者相比,≥60 岁的加奈珠单抗治疗患者的血压无临床意义的升高,治疗中出现的 AE、因 AE 停药、总体严重不良事件(SAE)或心血管 SAE 无增加频率。
年龄(至 65 岁)不影响偏头痛预防的疗效,对加奈珠单抗 PK 无临床意义的影响,无需调整剂量。此外,与年龄匹配的安慰剂治疗患者相比,≥60 岁的加奈珠单抗治疗患者的 AE 或血压升高频率无增加。
EVOLVE-1(NCT02614183,2015 年 11 月 23 日登记)、EVOLVE-2(NCT02614196,2015 年 11 月 23 日登记)、REGAIN(NCT02614261,2015 年 11 月 23 日登记)、ART-01(NCT01625988,2012 年 6 月 20 日登记)、I5Q-MC-CGAB(NCT02163993,2014 年 6 月 12 日登记)、I5Q-MC-CGAJ(NCT02614287,2015 年 11 月 23 日登记),均为回顾性登记。