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Abstract Details

Efficacy and tolerability of anti-CGRP monoclonal antibodies in patients aged ≥65 years with episodic or chronic migraine
Headache
P7 - Poster Session 7 (8:00 AM-9:00 AM)
2-012

To assess the efficacy and tolerability of three anti-CGRP monoclonal antibody (mAb) therapies (erenumab, fremanezumab, galcanezumab) in patients ≥65 years (O65) compared to patients <65 (U65) with episodic migraine (EM) and chronic migraine (CM).

Despite decreasing prevalence of migraine with advancing age, there still remains a significant proportion of individuals aged ≥65 years with migraine. Treatment of this population is difficult given associated numerous comorbidities, polypharmacy, and altered pharmacokinetics. This age group is often excluded from clinical trials, limiting evidence regarding efficacy, safety, and tolerability of migraine treatments.

Patients who were treated with an anti-CGRP mAb between June 2018 and December 2021 had their electronic medical records extracted. The cohort was grouped into daily (n=1303) and non-daily (n=1708) migraines, then further separated between O65 (n=304, 70.81 ± 4.74 years) or U65 (n=2707, 44.33 ± 11.71 years) at their treatment start date. The groups were compared with a Mann-Whitney test.

There was no significant difference (p=0.8247) in the migraine days reduced for non-daily migraine patients O65 (8.44 ± 6.70 less MMD) or U65 (8.37 ± 6.76 less MMD). There was not a significant difference (p=0.5853) in the reduction of migraine days for daily migraineurs O65 (12.53 ± 12.18 less MMD) or U65 (13.35 ± 11.72 less MMD). There were adverse reactions noted (95/3012,1.6% O65, 3.3% U65) with the most common side effects being injection site pain/reactions (38/95) and constipation (35/95). No serious adverse events were noted in our cohort in the 6 months of anti-CGRP mAb use.

This retrospective analysis provides real-world evidence that treatment with erenumab, fremanezumab, and galcanezumab is as efficacious and well-tolerated in patients O65 compared to patients U65 with EM or CM. This data may help guide choice of migraine treatment in older populations.

Authors/Disclosures
Sudipa Biswas, MD (Cleveland Clinic)
PRESENTER
Dr. Biswas has nothing to disclose.
Amira Salim (Cleveland Clinic Foundation - Main Campus) Miss Salim has nothing to disclose.
Elise R. Hennessy, MD (Penn State Health) Dr. Hennessy has nothing to disclose.
Aarushi Suneja, MD (Cleveland Clinic Foundation) Dr. Suneja has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Abbvie. Dr. Suneja has received personal compensation in the range of $5,000-$9,999 for serving on a Speakers Bureau for Abbvie.
Zubair Ahmed, MD (Apex Medical Research) Dr. Ahmed has received personal compensation in the range of $10,000-$49,999 for serving as a Consultant for Eli Lilly. Dr. Ahmed has received personal compensation in the range of $10,000-$49,999 for serving on a Speakers Bureau for Abbvie. Dr. Ahmed has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Biohaven.
No disclosure on file