Luigi Francesco Iannone, Marina Romozzi, Antonio Russo, Gennaro Saporito, Federico De Santis, Raffaele Ornello, Grazia Sances, Gloria Vaghi, Cristina Tassorelli, Maria Albanese, Simona Guerzoni, Alfonsina Casalena, Catello Vollono, Paolo Calabresi, Maria Pia Prudenzano, Edoardo Mampreso, Giorgio Dalla Volta, Maria Rosaria Valente, Gianluca Avino, Alberto Chiarugi, Simona Sacco, Francesca Pistoia, the Italian Headache Registry (RICe) study group
{"title":"抗降钙素基因相关肽与治疗不同疾病的其他单克隆抗体的关联:一项多中心、前瞻性、队列研究。","authors":"Luigi Francesco Iannone, Marina Romozzi, Antonio Russo, Gennaro Saporito, Federico De Santis, Raffaele Ornello, Grazia Sances, Gloria Vaghi, Cristina Tassorelli, Maria Albanese, Simona Guerzoni, Alfonsina Casalena, Catello Vollono, Paolo Calabresi, Maria Pia Prudenzano, Edoardo Mampreso, Giorgio Dalla Volta, Maria Rosaria Valente, Gianluca Avino, Alberto Chiarugi, Simona Sacco, Francesca Pistoia, the Italian Headache Registry (RICe) study group","doi":"10.1111/ene.16450","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background and purpose</h3>\n \n <p>Although there is extensive evidence about the safety of monoclonal antibodies against calcitonin gene-related peptide (anti-CGRP mAbs) in combination with traditional drugs, scarce data are available on the safety of their combination with other mAbs. This study aimed to evaluate the 6-month effectiveness and tolerability of anti-CGRP mAbs in combination with other mAbs for different diseases.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Patients included in the Italian Headache Registry and treated concomitantly with an anti-CGRP mAb and another mAb were included. Effectiveness outcomes for migraine included reduction from baseline of monthly headache days (MHDs), Migraine Disability Assessment (MIDAS) score, Headache Impact Test-6 (HIT-6) scores, and Patients' Global Impression of Change (PGIC) scale. Adverse events (AEs) were recorded.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Thirty-eight patients were included. In 27 patients (71.1%), the anti-CGRP mAb was added to a previously ongoing mAb. Nine patients (23.7%) discontinued one of the two mAbs before the end of treatment (seven discontinued the anti-CGRP mAb and two the other mAb). One patient discontinued for AEs. Anti-CGRP mAbs were discontinued due to ineffectiveness (<i>n</i> = 5, 55.5%) and one each (11.1%) for clinical remission and lost to follow-up. MHDs significantly decreased from baseline to 3 months (<i>p</i> < 0.0001) and 6 months (<i>p</i> < 0.001), as did the MIDAS and the HIT-6 scores at 3 and 6 months (<i>p</i> < 0.001). For anti-CGRP mAbs, 27.4% of patients reported PGIC ≥ 5 at 3 months and 48.3% at 6 months. Mild AEs associated with introduction of a second mAb were detected in six patients (15.8%).</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>In this real-world study, anti-CGRP mAbs showed safety and effectiveness when administered concomitantly with other mAbs.</p>\n </section>\n </div>","PeriodicalId":11954,"journal":{"name":"European Journal of Neurology","volume":"31 12","pages":""},"PeriodicalIF":4.5000,"publicationDate":"2024-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11555159/pdf/","citationCount":"0","resultStr":"{\"title\":\"Association of anti-calcitonin gene-related peptide with other monoclonal antibodies for different diseases: A multicenter, prospective, cohort study\",\"authors\":\"Luigi Francesco Iannone, Marina Romozzi, Antonio Russo, Gennaro Saporito, Federico De Santis, Raffaele Ornello, Grazia Sances, Gloria Vaghi, Cristina Tassorelli, Maria Albanese, Simona Guerzoni, Alfonsina Casalena, Catello Vollono, Paolo Calabresi, Maria Pia Prudenzano, Edoardo Mampreso, Giorgio Dalla Volta, Maria Rosaria Valente, Gianluca Avino, Alberto Chiarugi, Simona Sacco, Francesca Pistoia, the Italian Headache Registry (RICe) study group\",\"doi\":\"10.1111/ene.16450\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background and purpose</h3>\\n \\n <p>Although there is extensive evidence about the safety of monoclonal antibodies against calcitonin gene-related peptide (anti-CGRP mAbs) in combination with traditional drugs, scarce data are available on the safety of their combination with other mAbs. This study aimed to evaluate the 6-month effectiveness and tolerability of anti-CGRP mAbs in combination with other mAbs for different diseases.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>Patients included in the Italian Headache Registry and treated concomitantly with an anti-CGRP mAb and another mAb were included. Effectiveness outcomes for migraine included reduction from baseline of monthly headache days (MHDs), Migraine Disability Assessment (MIDAS) score, Headache Impact Test-6 (HIT-6) scores, and Patients' Global Impression of Change (PGIC) scale. Adverse events (AEs) were recorded.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Thirty-eight patients were included. In 27 patients (71.1%), the anti-CGRP mAb was added to a previously ongoing mAb. Nine patients (23.7%) discontinued one of the two mAbs before the end of treatment (seven discontinued the anti-CGRP mAb and two the other mAb). One patient discontinued for AEs. Anti-CGRP mAbs were discontinued due to ineffectiveness (<i>n</i> = 5, 55.5%) and one each (11.1%) for clinical remission and lost to follow-up. MHDs significantly decreased from baseline to 3 months (<i>p</i> < 0.0001) and 6 months (<i>p</i> < 0.001), as did the MIDAS and the HIT-6 scores at 3 and 6 months (<i>p</i> < 0.001). For anti-CGRP mAbs, 27.4% of patients reported PGIC ≥ 5 at 3 months and 48.3% at 6 months. 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Association of anti-calcitonin gene-related peptide with other monoclonal antibodies for different diseases: A multicenter, prospective, cohort study
Background and purpose
Although there is extensive evidence about the safety of monoclonal antibodies against calcitonin gene-related peptide (anti-CGRP mAbs) in combination with traditional drugs, scarce data are available on the safety of their combination with other mAbs. This study aimed to evaluate the 6-month effectiveness and tolerability of anti-CGRP mAbs in combination with other mAbs for different diseases.
Methods
Patients included in the Italian Headache Registry and treated concomitantly with an anti-CGRP mAb and another mAb were included. Effectiveness outcomes for migraine included reduction from baseline of monthly headache days (MHDs), Migraine Disability Assessment (MIDAS) score, Headache Impact Test-6 (HIT-6) scores, and Patients' Global Impression of Change (PGIC) scale. Adverse events (AEs) were recorded.
Results
Thirty-eight patients were included. In 27 patients (71.1%), the anti-CGRP mAb was added to a previously ongoing mAb. Nine patients (23.7%) discontinued one of the two mAbs before the end of treatment (seven discontinued the anti-CGRP mAb and two the other mAb). One patient discontinued for AEs. Anti-CGRP mAbs were discontinued due to ineffectiveness (n = 5, 55.5%) and one each (11.1%) for clinical remission and lost to follow-up. MHDs significantly decreased from baseline to 3 months (p < 0.0001) and 6 months (p < 0.001), as did the MIDAS and the HIT-6 scores at 3 and 6 months (p < 0.001). For anti-CGRP mAbs, 27.4% of patients reported PGIC ≥ 5 at 3 months and 48.3% at 6 months. Mild AEs associated with introduction of a second mAb were detected in six patients (15.8%).
Conclusions
In this real-world study, anti-CGRP mAbs showed safety and effectiveness when administered concomitantly with other mAbs.
期刊介绍:
The European Journal of Neurology is the official journal of the European Academy of Neurology and covers all areas of clinical and basic research in neurology, including pre-clinical research of immediate translational value for new potential treatments. Emphasis is placed on major diseases of large clinical and socio-economic importance (dementia, stroke, epilepsy, headache, multiple sclerosis, movement disorders, and infectious diseases).