Real-world impact of fremanezumab on migraine symptoms and resource utilization in the United States
- PMID: 34930112
- PMCID: PMC8903530
- DOI: 10.1186/s10194-021-01358-9
Real-world impact of fremanezumab on migraine symptoms and resource utilization in the United States
Abstract
Background: Fremanezumab, a fully humanized monoclonal antibody (IgG2Δa) that selectively targets calcitonin gene-related peptide (CGRP), is approved for migraine prevention in adults. Real-world data on the effectiveness of fremanezumab are limited. This retrospective, observational cohort study assessed patient-reported migraine symptoms, health care resource utilization (HCRU), and direct medical costs before and after fremanezumab treatment initiation.
Methods: Data were extracted from September 2018 through June 2020 from the Midwest component of EMRClaims+®, an integrated health services database containing > 20 million medical records from national commercial insurance claims, Medicare claims, and regional electronic medical records. Patients included in the cohort analysis were aged ≥ 18 years and were administered fremanezumab, with enrollment or treatment history for ≥ 6 months prior (pre-index) to initiating fremanezumab (index date) and ≥ 1 month after the index date (post-index), and without pregnancy or pregnancy-related encounters during the study period. Patient-reported headache frequency, migraine pain intensity (MPI), composite migraine symptoms, and HCRU were assessed pre-index and ≥ 1 month after fremanezumab initiation. Wilcoxon signed-rank tests were used to compare means of migraine symptoms and outcomes and HCRU before and after fremanezumab initiation.
Results: Overall, 172 patients were eligible for analysis. Of patients who self-reported (n = 129), 83.7% reported improvement in headache frequency or symptoms after fremanezumab treatment. Specifically, headache frequency decreased by 63% after fremanezumab initiation: mean (standard deviation) headache frequency was 22.24 (9.29) days per month pre-index versus 8.24 (7.42) days per month post-index (P < 0.0001). Mean MPI also decreased by 18% after fremanezumab initiation: MPI was 5.47 (3.19) pre-index versus 4.51 (3.34) post-index (P = 0.014). Mean emergency room (ER) visits per month decreased from 0.72 to 0.54 (P = 0.003), and mean outpatient visits per month decreased from 1.04 to 0.81 (P < 0.001). Mean hospitalizations per month decreased, but the results did not reach statistical significance (P = 0.095). Hospitalization and ER costs decreased, while outpatient costs increased, from pre-index to post-index, but differences were not statistically significant (P ≥ 0.232).
Conclusions: Significant reductions in headache frequency, MPI, and HCRU were observed after fremanezumab initiation in patients with migraine in a US real-world setting.
Keywords: Fremanezumab; Headache frequency; Health care resource utilization; Migraine; Migraine pain intensity; Real-world efficacy.
© 2021. The Author(s).
Conflict of interest statement
PM has received research support from Amgen, Novartis, Eli Lilly, Teva Pharmaceuticals, and Alder BioPharmaceuticals; and serves as a consultant for Amgen, Novartis, Eli Lilly, Teva Pharmaceuticals, and Alder BioPharmaceuticals. LL is an employee of Henry Ford Health System, with research funding from eMAX Health Systems. JC and ZD are employees of eMAX Health Systems. LJK, ST, and MD are employees of Teva Pharmaceuticals. JMC and KT are former employees of Teva Pharmaceuticals. AM has nothing to disclose.
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