Scuteri Damiana, Lawrence Gary W, Iannacchero Rosario, Trimboli Michele, Nicotera Pierluigi, Corasaniti Maria T, Bagetta Giacinto
Department of Health Sciences, University "Magna Graecia" of Catanzaro, Catanzaro, Italy.
Department of Biotechnology, Dublin City University, Dublin, Ireland.
Pain Manag. 2025 Apr;15(4):177-181. doi: 10.1080/17581869.2025.2487413. Epub 2025 Apr 1.
Chronic migraine is a disabling neurovascular disorder that represents the leading cause of years lived with disability in people under 50 with a remarkable social burden due to widespread resistance to the front-line treatments used routinely in current clinical practice. The present study investigates the efficacy and safety of combination therapy using eptinezumab and erenumab, recently approved monoclonal antibodies (mAbs) directed against calcitonin gene-related peptide or its receptor, respectively, or the receptor competitive antagonist atogepant together with botulinum toxin type A in chronic migraine that has proven resistant to front-line treatments for at least 6 weeks. To this aim a retrospective and a prospective phase are designed. Furthermore, a feasible salivary biomarker of migraine is under investigation in the prospective stage of the study. Based on recent expert opinions supporting the switch to easy-to-use small molecule calcitonin gene-related peptide (CGRP)-targeting, i.e. rimegepant or atogepant in unresponsive patients, the present study may offer to clinicians a novel treatment to enhance the therapeutic preventive machinery in chronic migraine.
慢性偏头痛是一种致残性神经血管疾病,是50岁以下人群中导致失能生存年数的主要原因,由于对当前临床实践中常规使用的一线治疗普遍存在耐药性,其社会负担显著。本研究调查了eptinezumab和erenumab联合治疗的疗效和安全性,这两种药物是最近分别获批的针对降钙素基因相关肽(CGRP)或其受体的单克隆抗体(mAbs),以及受体竞争性拮抗剂atogepant与A型肉毒毒素联合用于对一线治疗至少6周耐药的慢性偏头痛患者。为此,设计了一个回顾性阶段和一个前瞻性阶段。此外,在研究的前瞻性阶段正在研究一种可行的偏头痛唾液生物标志物。基于最近支持转向使用易于使用的小分子CGRP靶向药物(即对无反应患者使用rimegepant或atogepant)的专家意见,本研究可能为临床医生提供一种新的治疗方法,以增强慢性偏头痛的治疗预防机制。