4.4 Article

Pre-treatment non-ictal cephalic allodynia identifies responders to prophylactic treatment of chronic and episodic migraine patients with galcanezumab: A prospective quantitative sensory testing study (NCT04271202)

Journal

CEPHALALGIA
Volume 43, Issue 3, Pages -

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/03331024221147881

Keywords

Allodynia; galcanezumab; headache; trigeminal; CGRP monoclonal antibodies

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This study used quantitative sensory testing to analyze the presence of cephalic and extracephalic allodynia in the pre-treatment non-ictal phase of migraine patients. The results showed that the presence of cephalic allodynia was highly correlated with the response to galcanezumab treatment, suggesting that it can be used to predict the treatment outcome.
BackgroundMigraine is a complex neurological disorder involving generalized abnormalities in processing sensory information. Adopting evidence that central sensitization imposes major hurdles in the treatment of migraine, we hypothesized that it is the non-ictal (rather than ictal) allodynia that may determine the outcome of migraine prevention with peripherally-acting drugs. MethodsTo test this hypothesis, we used Quantitative Sensory Testing to determine whether it is possible to identify a patient's response to prophylactic treatment with galcanezumab based on presence/absence of cephalic and/or extracephalic allodynia during the pre-treatment non-ictal phase of migraine. ResultsUsing strict criteria for allodynia (heat 32-40 degrees C, cold 32-20 degrees C, mechanical <60 g), we report that (a) the incidence of pre-treatment non-ictal cephalic allodynia was 21% in the 24 responders (>50% decrease in monthly migraine days) and 85% in the 19 non-responders; (b) the incidence of non-ictal extracephalic allodynia distinguishes responders from non-responders less accurately; and that (c) the incidence of non-ictal cephalic allodynia was similar in the chronic migraine and high-frequency episodic migraine groups. ConclusionsClinically, the findings suggest that presence/absence of non-ictal allodynia can be used to identify galcanezumab responders with nearly 80% accuracy and galcanezumab non-responders with nearly 85% accuracy. Mechanistically, the presence of non-ictal allodynia (reflecting a state of activity-independent central sensitization) in both chronic migraine and high-frequency episodic migraine patients raises the possibility that the state of non-ictal allodynia may be attributed to physiological properties of central trigeminovascular neurons that are due to the genetic load of the individual patient rather than their migraine frequency.

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