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Observational Study
. 2023 Sep 12;101(11):482-488.
doi: 10.1212/WNL.0000000000207292. Epub 2023 Apr 18.

Late Response to Anti-CGRP Monoclonal Antibodies in Migraine: A Multicenter Prospective Observational Study

Collaborators, Affiliations
Observational Study

Late Response to Anti-CGRP Monoclonal Antibodies in Migraine: A Multicenter Prospective Observational Study

Piero Barbanti et al. Neurology. .

Abstract

Objectives: To assess the frequency and characteristics of late responders (>12 weeks) to monoclonal antibodies (mAbs) targeting the calcitonin gene-related peptide (CGRP).

Methods: This is a multicenter (n = 16) prospective real-life study considering all consecutive adults with high-frequency or chronic migraine treated with anti-CGRP mAbs for ≥24 weeks. We defined responder patients with a ≥50% reduction from baseline in monthly migraine/headache days at weeks 9-12 and late responders as those achieving a ≥50% reduction only afterward.

Results: A total of 771 people with migraine completed ≥24 weeks of anti-CGRP mAb treatment. Responders at 12 weeks were 65.6% (506/771) of the patients, while nonresponders were 34.4% (265/771). A total of 146 of the 265 nonresponders (55.1%) at 12 weeks responded afterward (late responders): they differed from responders for a higher BMI (+0.78, 95% CI [0.10; 1.45]; p = 0.024), more frequent treatment failures (+0.52, 95% CI [0.09; 0.95]; p = 0.017) and psychiatric comorbidities (+10.1%, 95% CI [0.1; 0.20]; p = 0.041), and less common unilateral pain, alone (-10,9%, 95% CI [-20.5; -1.2]; p = 0.025) or in combination with unilateral cranial autonomic symptoms (-12.3%, 95% CI [-20.2;-3.9]; p = 0.006) or allodynia (-10.7, 95% CI [-18.2; -3.2]; p = 0.01).

Discussion: Half of nonresponders to anti-CGRP mAbs at 12 weeks are indeed late responders. Efficacy of anti-CGRP mAbs should be assessed at 24 weeks while treatment duration should be extended beyond 12 months.

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Conflict of interest statement

Piero Barbanti received travel grants and honoraria for participating in advisory boards, speaker panels, or clinical investigation studies from Alder, Allergan, Angelini, Assosalute, Bayer, ElectroCore, Eli-Lilly, GSK, Lundbeck, Lusofarmaco, 1MED, MSD, New Penta, Noema Pharma, Novartis, Stx-Med, Teva, Visufarma, and Zambon. Cinzia Aurilia received travel grants from FB-Health, Lusofarmaco, Almirall, Eli-Lilly Novartis and Teva; Gabriella Egeo received travel grants and honoraria from Eli-Lilly, Novartis, New Penta, and Ecupharma; Paola Torelli received travel grants and honoraria as a speaker or for participating in advisory boards from Novartis, Teva, Eli Lilly, and Allergan; Stefania Proietti has no disclosures to declare; Sabina Cevoli received honoraria for participating in speaker panels from Teva and Novartis. Stefano Bonassi has no disclosures to declare. Go to Neurology.org/N for full disclosures.

Figures

Figure
Figure. Proportion of Patients With a 50% or Greater Reduction in Monthly Migraine/Headache Days After Treatment With Anti-CGRPmAbs
(A): all patients; (B): high-frequency episodic migraine (HFEM); (C): chronic migraine (CM). Gray bars: responders (≤12 weeks); white bars: nonresponders; black bars: late responders (>12 weeks).

References

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