CGRP-Targeted Therapy for Episodic and Chronic Cluster Headache.

Curr Pain Headache Rep

Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, No. 201, Sec. 2, Shi-Pai Rd, Taipei, Taiwan, 11217.

Published: September 2022

AI Article Synopsis

  • This review highlights the ongoing challenges in effectively treating chronic cluster headache (CH) and focuses on new treatment options targeting calcitonin gene-related peptide (CGRP) and its receptors.
  • Two anti-CGRP monoclonal antibodies, galcanezumab and fremanezumab, were tested in trials for their effectiveness in preventing CH, with galcanezumab showing some efficacy for episodic CH but not for chronic CH, while fremanezumab was ineffective for both types.
  • The differences in treatment outcomes may be related to study design and the varying roles of CGRP in chronic CH, highlighting the need for further research in this area.

Article Abstract

Purpose Of Review: Chronic cluster headache (CH) substantially affects patients' quality of life, and treatment remains challenging. The current article reviewed controlled studies for new treatment options targeting calcitonin gene-related peptide (CGRP) or its receptors in CH and discussed the current gaps and future directions for the treatment of chronic CH.

Recent Findings: Two anti-CGRP monoclonal antibodies (i.e., galcanezumab and fremanezumab) completed randomized-control trials for efficacy for the preventive treatment of episodic and chronic CH. Galcanezumab was effective for preventing episodic CH but not chronic CH. Fremanezumab was ineffective in preventing episodic and chronic CH. Studies for other anti-CGRP monoclonal antibodies and CGRP antagonists are still pending for results. There are no randomized controlled trials for CGRP-targeted therapies that showed efficacy for chronic CH prevention. The different responses to galcanezumab between episodic and chronic CH may be due to the study design, i.e., the allowance of concomitant preventive therapies in the chronic CH study but not in the episodic CH study. Another reason for the discrepancies is the different roles and sensitivity of CGRP in chronic CH.

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Source
http://dx.doi.org/10.1007/s11916-022-01070-6DOI Listing

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