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Ultra-late response (> 24 weeks) to anti-CGRP monoclonal antibodies in migraine: a multicenter, prospective, observational study

Objective Nearly 60% of migraine patients treated with monoclonal antibodies (mAbs) targeting the calcitonin gene-related peptide (CGRP) pathway experience a ≥ 50% reduction in monthly migraine days (MMD) at 12 weeks compared to baseline (responders) . However, approximately half of the patients not...

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Published in:Journal of neurology 2024-05, Vol.271 (5), p.2434-2443
Main Authors: Barbanti, Piero, Aurilia, Cinzia, Egeo, Gabriella, Proietti, Stefania, D’Onofrio, Florindo, Torelli, Paola, Aguggia, Marco, Bertuzzo, Davide, Finocchi, Cinzia, Trimboli, Michele, Cevoli, Sabina, Fiorentini, Giulia, Orlando, Bianca, Zucco, Maurizio, Di Clemente, Laura, Cetta, Ilaria, Colombo, Bruno, di Poggio, Monica Laura Bandettini, Favoni, Valentina, Grazzi, Licia, Salerno, Antonio, Carnevale, Antonio, Robotti, Micaela, Frediani, Fabio, Altamura, Claudia, Filippi, Massimo, Vernieri, Fabrizio, Bonassi, Stefano
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cited_by cdi_FETCH-LOGICAL-c475t-acd38eef7f8c6bd343f203e494150a633a2ffaf3e3e1c8b328bbf5a7809ba1763
cites cdi_FETCH-LOGICAL-c475t-acd38eef7f8c6bd343f203e494150a633a2ffaf3e3e1c8b328bbf5a7809ba1763
container_end_page 2443
container_issue 5
container_start_page 2434
container_title Journal of neurology
container_volume 271
creator Barbanti, Piero
Aurilia, Cinzia
Egeo, Gabriella
Proietti, Stefania
D’Onofrio, Florindo
Torelli, Paola
Aguggia, Marco
Bertuzzo, Davide
Finocchi, Cinzia
Trimboli, Michele
Cevoli, Sabina
Fiorentini, Giulia
Orlando, Bianca
Zucco, Maurizio
Di Clemente, Laura
Cetta, Ilaria
Colombo, Bruno
di Poggio, Monica Laura Bandettini
Favoni, Valentina
Grazzi, Licia
Salerno, Antonio
Carnevale, Antonio
Robotti, Micaela
Frediani, Fabio
Altamura, Claudia
Filippi, Massimo
Vernieri, Fabrizio
Bonassi, Stefano
description Objective Nearly 60% of migraine patients treated with monoclonal antibodies (mAbs) targeting the calcitonin gene-related peptide (CGRP) pathway experience a ≥ 50% reduction in monthly migraine days (MMD) at 12 weeks compared to baseline (responders) . However, approximately half of the patients not responding to anti-CGRP mAbs ≤ 12 weeks do respond ≤ 24 weeks ( late responders) . We assessed frequency and characteristics of patients responding to anti-CGRP mAbs only > 24 weeks ( ultra-late responders ). Methods In this multicenter ( n  = 16), prospective, observational, real-life study, we enrolled all consecutive adults affected by high-frequency episodic migraine (HFEM: ≥ 8 days/month) or chronic migraine (CM), with ≥ 3 prior therapeutic failures, treated with any anti-CGRP mAbs for ≥ 48 weeks. We defined responders patients with a ≥ 50% response rate ≤ 12 weeks, late responders those with a ≥ 50% response rate ≤ 24 weeks, and ultra-late responders those achieving a ≥ 50% response only > 24 weeks. Results A total of 572 migraine patients completed ≥ 48 weeks of anti-CGRP mAbs treatment. Responders accounted for 60.5% (346/572), late responders for 15% (86/572), and ultra-late responders for 15.7% (90/572). Among ultra-late responders , 7.3% (42/572) maintained the ≥ 50% response rate across all subsequent time intervals (weeks 28, 32, 36, 40, 44, and 48) and were considered persistent ultra-late responders , while 8.4% (48/572) missed the ≥ 50% response rate at ≥ 1 subsequent time interval and were classified as fluctuating ultra-late responders . Fifty patients (8.7%) did not respond at any time interval ≤ 48 weeks. Ultra-late responders differed from responders for higher BMI ( p  = 0.033), longer duration of medication overuse ( p  
doi_str_mv 10.1007/s00415-023-12103-4
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However, approximately half of the patients not responding to anti-CGRP mAbs ≤ 12 weeks do respond ≤ 24 weeks ( late responders) . We assessed frequency and characteristics of patients responding to anti-CGRP mAbs only &gt; 24 weeks ( ultra-late responders ). Methods In this multicenter ( n  = 16), prospective, observational, real-life study, we enrolled all consecutive adults affected by high-frequency episodic migraine (HFEM: ≥ 8 days/month) or chronic migraine (CM), with ≥ 3 prior therapeutic failures, treated with any anti-CGRP mAbs for ≥ 48 weeks. We defined responders patients with a ≥ 50% response rate ≤ 12 weeks, late responders those with a ≥ 50% response rate ≤ 24 weeks, and ultra-late responders those achieving a ≥ 50% response only &gt; 24 weeks. Results A total of 572 migraine patients completed ≥ 48 weeks of anti-CGRP mAbs treatment. Responders accounted for 60.5% (346/572), late responders for 15% (86/572), and ultra-late responders for 15.7% (90/572). Among ultra-late responders , 7.3% (42/572) maintained the ≥ 50% response rate across all subsequent time intervals (weeks 28, 32, 36, 40, 44, and 48) and were considered persistent ultra-late responders , while 8.4% (48/572) missed the ≥ 50% response rate at ≥ 1 subsequent time interval and were classified as fluctuating ultra-late responders . Fifty patients (8.7%) did not respond at any time interval ≤ 48 weeks. Ultra-late responders differed from responders for higher BMI ( p  = 0.033), longer duration of medication overuse ( p  &lt; 0.001), lower NRS ( p  = 0.017) and HIT-6 scores ( p  = 0.002), higher frequency of dopaminergic symptoms ( p  = 0.002), less common unilateral pain—either alone ( p  = 0.010) or in combination with UAS ( p  = 0.023), allodynia ( p  = 0.043), or UAS and allodynia ( p  = 0.012)—a higher number of comorbidities ( p  = 0.012), psychiatric comorbidities ( p  = 0.010) and a higher proportion of patients with ≥ 1 comorbidity ( p  = 0.020). Conclusion Two-thirds of patients not responding to anti-CGRP mAbs ≤ 24 weeks do respond later, while non-responders  ≤ 48 weeks are quite rare (8.7%). These findings suggest to rethink the duration of migraine prophylaxis and the definition of resistant and refractory migraine, currently based on the response after 2–3 months of treatment.</description><identifier>ISSN: 0340-5354</identifier><identifier>ISSN: 1432-1459</identifier><identifier>EISSN: 1432-1459</identifier><identifier>DOI: 10.1007/s00415-023-12103-4</identifier><identifier>PMID: 38231271</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Calcitonin ; Calcitonin gene-related peptide ; Comorbidity ; Dopamine receptors ; Headache ; Medicine ; Medicine &amp; Public Health ; Migraine ; Monoclonal antibodies ; Neurology ; Neuroradiology ; Neurosciences ; Original Communication ; Pain perception ; Prophylaxis ; Response rates</subject><ispartof>Journal of neurology, 2024-05, Vol.271 (5), p.2434-2443</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-acd38eef7f8c6bd343f203e494150a633a2ffaf3e3e1c8b328bbf5a7809ba1763</citedby><cites>FETCH-LOGICAL-c475t-acd38eef7f8c6bd343f203e494150a633a2ffaf3e3e1c8b328bbf5a7809ba1763</cites><orcidid>0000-0002-5670-3755</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38231271$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Barbanti, Piero</creatorcontrib><creatorcontrib>Aurilia, Cinzia</creatorcontrib><creatorcontrib>Egeo, Gabriella</creatorcontrib><creatorcontrib>Proietti, Stefania</creatorcontrib><creatorcontrib>D’Onofrio, Florindo</creatorcontrib><creatorcontrib>Torelli, Paola</creatorcontrib><creatorcontrib>Aguggia, Marco</creatorcontrib><creatorcontrib>Bertuzzo, Davide</creatorcontrib><creatorcontrib>Finocchi, Cinzia</creatorcontrib><creatorcontrib>Trimboli, Michele</creatorcontrib><creatorcontrib>Cevoli, Sabina</creatorcontrib><creatorcontrib>Fiorentini, Giulia</creatorcontrib><creatorcontrib>Orlando, Bianca</creatorcontrib><creatorcontrib>Zucco, Maurizio</creatorcontrib><creatorcontrib>Di Clemente, Laura</creatorcontrib><creatorcontrib>Cetta, Ilaria</creatorcontrib><creatorcontrib>Colombo, Bruno</creatorcontrib><creatorcontrib>di Poggio, Monica Laura Bandettini</creatorcontrib><creatorcontrib>Favoni, Valentina</creatorcontrib><creatorcontrib>Grazzi, Licia</creatorcontrib><creatorcontrib>Salerno, Antonio</creatorcontrib><creatorcontrib>Carnevale, Antonio</creatorcontrib><creatorcontrib>Robotti, Micaela</creatorcontrib><creatorcontrib>Frediani, Fabio</creatorcontrib><creatorcontrib>Altamura, Claudia</creatorcontrib><creatorcontrib>Filippi, Massimo</creatorcontrib><creatorcontrib>Vernieri, Fabrizio</creatorcontrib><creatorcontrib>Bonassi, Stefano</creatorcontrib><creatorcontrib>ERT; for the Italian Migraine Registry study group</creatorcontrib><creatorcontrib>ERT; for the Italian Migraine Registry study group</creatorcontrib><title>Ultra-late response (&gt; 24 weeks) to anti-CGRP monoclonal antibodies in migraine: a multicenter, prospective, observational study</title><title>Journal of neurology</title><addtitle>J Neurol</addtitle><addtitle>J Neurol</addtitle><description>Objective Nearly 60% of migraine patients treated with monoclonal antibodies (mAbs) targeting the calcitonin gene-related peptide (CGRP) pathway experience a ≥ 50% reduction in monthly migraine days (MMD) at 12 weeks compared to baseline (responders) . However, approximately half of the patients not responding to anti-CGRP mAbs ≤ 12 weeks do respond ≤ 24 weeks ( late responders) . We assessed frequency and characteristics of patients responding to anti-CGRP mAbs only &gt; 24 weeks ( ultra-late responders ). Methods In this multicenter ( n  = 16), prospective, observational, real-life study, we enrolled all consecutive adults affected by high-frequency episodic migraine (HFEM: ≥ 8 days/month) or chronic migraine (CM), with ≥ 3 prior therapeutic failures, treated with any anti-CGRP mAbs for ≥ 48 weeks. We defined responders patients with a ≥ 50% response rate ≤ 12 weeks, late responders those with a ≥ 50% response rate ≤ 24 weeks, and ultra-late responders those achieving a ≥ 50% response only &gt; 24 weeks. Results A total of 572 migraine patients completed ≥ 48 weeks of anti-CGRP mAbs treatment. Responders accounted for 60.5% (346/572), late responders for 15% (86/572), and ultra-late responders for 15.7% (90/572). Among ultra-late responders , 7.3% (42/572) maintained the ≥ 50% response rate across all subsequent time intervals (weeks 28, 32, 36, 40, 44, and 48) and were considered persistent ultra-late responders , while 8.4% (48/572) missed the ≥ 50% response rate at ≥ 1 subsequent time interval and were classified as fluctuating ultra-late responders . Fifty patients (8.7%) did not respond at any time interval ≤ 48 weeks. Ultra-late responders differed from responders for higher BMI ( p  = 0.033), longer duration of medication overuse ( p  &lt; 0.001), lower NRS ( p  = 0.017) and HIT-6 scores ( p  = 0.002), higher frequency of dopaminergic symptoms ( p  = 0.002), less common unilateral pain—either alone ( p  = 0.010) or in combination with UAS ( p  = 0.023), allodynia ( p  = 0.043), or UAS and allodynia ( p  = 0.012)—a higher number of comorbidities ( p  = 0.012), psychiatric comorbidities ( p  = 0.010) and a higher proportion of patients with ≥ 1 comorbidity ( p  = 0.020). Conclusion Two-thirds of patients not responding to anti-CGRP mAbs ≤ 24 weeks do respond later, while non-responders  ≤ 48 weeks are quite rare (8.7%). These findings suggest to rethink the duration of migraine prophylaxis and the definition of resistant and refractory migraine, currently based on the response after 2–3 months of treatment.</description><subject>Calcitonin</subject><subject>Calcitonin gene-related peptide</subject><subject>Comorbidity</subject><subject>Dopamine receptors</subject><subject>Headache</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Migraine</subject><subject>Monoclonal antibodies</subject><subject>Neurology</subject><subject>Neuroradiology</subject><subject>Neurosciences</subject><subject>Original Communication</subject><subject>Pain perception</subject><subject>Prophylaxis</subject><subject>Response rates</subject><issn>0340-5354</issn><issn>1432-1459</issn><issn>1432-1459</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9UctuFDEQtBCILIEf4IAscQlSDH7uzHAAoRUEpEggRM6Wx9OzOMzYg-1ZlBsSJ_6Cb-FT-BK8uyE8Dpxa6qquru5C6C6jDxml1aNEqWSKUC4I44wKIq-hBZOCEyZVcx0tqJCUKKHkAbqV0jmltC7ATXQgai4Yr9gCfTkbcjRkMBlwhDQFnwAfPfnx-SuX3799AviQHuAcsPHZkdXJ2zd4DD7YIXgz7Jpt6Bwk7Dwe3Toa5-ExNnich-ws-AzxGE8xpAlsdhs4xqFNEDcmu51CynN3cRvd6M2Q4M5lPURnL56_W70kp69PXq2enRIrK5WJsZ2oAfqqr-2y7YQUPacCZFOeQM1SCMP73vQCBDBbt4LXbdsrU9W0aQ2rluIQPd3rTnM7Qre1F82gp-hGEy90ME7_jXj3Xq_DRjNGlapqVRSOLhVi-DhDynp0ycIwGA9hTpo3TDV1w9h22f1_qOdhjuXmpAWVVfHMaVVYfM-y5UcpQn_lhlG9DVnvQ9YlZL0LWcsydO_PO65GfqVaCGJPSAXya4i_d_9H9ifXibYH</recordid><startdate>20240501</startdate><enddate>20240501</enddate><creator>Barbanti, Piero</creator><creator>Aurilia, Cinzia</creator><creator>Egeo, Gabriella</creator><creator>Proietti, Stefania</creator><creator>D’Onofrio, Florindo</creator><creator>Torelli, Paola</creator><creator>Aguggia, Marco</creator><creator>Bertuzzo, Davide</creator><creator>Finocchi, Cinzia</creator><creator>Trimboli, Michele</creator><creator>Cevoli, Sabina</creator><creator>Fiorentini, Giulia</creator><creator>Orlando, Bianca</creator><creator>Zucco, Maurizio</creator><creator>Di Clemente, Laura</creator><creator>Cetta, Ilaria</creator><creator>Colombo, Bruno</creator><creator>di Poggio, Monica Laura Bandettini</creator><creator>Favoni, Valentina</creator><creator>Grazzi, Licia</creator><creator>Salerno, Antonio</creator><creator>Carnevale, Antonio</creator><creator>Robotti, Micaela</creator><creator>Frediani, Fabio</creator><creator>Altamura, Claudia</creator><creator>Filippi, Massimo</creator><creator>Vernieri, Fabrizio</creator><creator>Bonassi, Stefano</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5670-3755</orcidid></search><sort><creationdate>20240501</creationdate><title>Ultra-late response (&gt; 24 weeks) to anti-CGRP monoclonal antibodies in migraine: a multicenter, prospective, observational study</title><author>Barbanti, Piero ; Aurilia, Cinzia ; Egeo, Gabriella ; Proietti, Stefania ; D’Onofrio, Florindo ; Torelli, Paola ; Aguggia, Marco ; Bertuzzo, Davide ; Finocchi, Cinzia ; Trimboli, Michele ; Cevoli, Sabina ; Fiorentini, Giulia ; Orlando, Bianca ; Zucco, Maurizio ; Di Clemente, Laura ; Cetta, Ilaria ; Colombo, Bruno ; di Poggio, Monica Laura Bandettini ; Favoni, Valentina ; Grazzi, Licia ; Salerno, Antonio ; Carnevale, Antonio ; Robotti, Micaela ; Frediani, Fabio ; Altamura, Claudia ; Filippi, Massimo ; Vernieri, Fabrizio ; Bonassi, Stefano</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-acd38eef7f8c6bd343f203e494150a633a2ffaf3e3e1c8b328bbf5a7809ba1763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Calcitonin</topic><topic>Calcitonin gene-related peptide</topic><topic>Comorbidity</topic><topic>Dopamine receptors</topic><topic>Headache</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Migraine</topic><topic>Monoclonal antibodies</topic><topic>Neurology</topic><topic>Neuroradiology</topic><topic>Neurosciences</topic><topic>Original Communication</topic><topic>Pain perception</topic><topic>Prophylaxis</topic><topic>Response rates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barbanti, Piero</creatorcontrib><creatorcontrib>Aurilia, Cinzia</creatorcontrib><creatorcontrib>Egeo, Gabriella</creatorcontrib><creatorcontrib>Proietti, Stefania</creatorcontrib><creatorcontrib>D’Onofrio, Florindo</creatorcontrib><creatorcontrib>Torelli, Paola</creatorcontrib><creatorcontrib>Aguggia, Marco</creatorcontrib><creatorcontrib>Bertuzzo, Davide</creatorcontrib><creatorcontrib>Finocchi, Cinzia</creatorcontrib><creatorcontrib>Trimboli, Michele</creatorcontrib><creatorcontrib>Cevoli, Sabina</creatorcontrib><creatorcontrib>Fiorentini, Giulia</creatorcontrib><creatorcontrib>Orlando, Bianca</creatorcontrib><creatorcontrib>Zucco, Maurizio</creatorcontrib><creatorcontrib>Di Clemente, Laura</creatorcontrib><creatorcontrib>Cetta, Ilaria</creatorcontrib><creatorcontrib>Colombo, Bruno</creatorcontrib><creatorcontrib>di Poggio, Monica Laura Bandettini</creatorcontrib><creatorcontrib>Favoni, Valentina</creatorcontrib><creatorcontrib>Grazzi, Licia</creatorcontrib><creatorcontrib>Salerno, Antonio</creatorcontrib><creatorcontrib>Carnevale, Antonio</creatorcontrib><creatorcontrib>Robotti, Micaela</creatorcontrib><creatorcontrib>Frediani, Fabio</creatorcontrib><creatorcontrib>Altamura, Claudia</creatorcontrib><creatorcontrib>Filippi, Massimo</creatorcontrib><creatorcontrib>Vernieri, Fabrizio</creatorcontrib><creatorcontrib>Bonassi, Stefano</creatorcontrib><creatorcontrib>ERT; 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for the Italian Migraine Registry study group</aucorp><aucorp>ERT; for the Italian Migraine Registry study group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ultra-late response (&gt; 24 weeks) to anti-CGRP monoclonal antibodies in migraine: a multicenter, prospective, observational study</atitle><jtitle>Journal of neurology</jtitle><stitle>J Neurol</stitle><addtitle>J Neurol</addtitle><date>2024-05-01</date><risdate>2024</risdate><volume>271</volume><issue>5</issue><spage>2434</spage><epage>2443</epage><pages>2434-2443</pages><issn>0340-5354</issn><issn>1432-1459</issn><eissn>1432-1459</eissn><abstract>Objective Nearly 60% of migraine patients treated with monoclonal antibodies (mAbs) targeting the calcitonin gene-related peptide (CGRP) pathway experience a ≥ 50% reduction in monthly migraine days (MMD) at 12 weeks compared to baseline (responders) . However, approximately half of the patients not responding to anti-CGRP mAbs ≤ 12 weeks do respond ≤ 24 weeks ( late responders) . We assessed frequency and characteristics of patients responding to anti-CGRP mAbs only &gt; 24 weeks ( ultra-late responders ). Methods In this multicenter ( n  = 16), prospective, observational, real-life study, we enrolled all consecutive adults affected by high-frequency episodic migraine (HFEM: ≥ 8 days/month) or chronic migraine (CM), with ≥ 3 prior therapeutic failures, treated with any anti-CGRP mAbs for ≥ 48 weeks. We defined responders patients with a ≥ 50% response rate ≤ 12 weeks, late responders those with a ≥ 50% response rate ≤ 24 weeks, and ultra-late responders those achieving a ≥ 50% response only &gt; 24 weeks. Results A total of 572 migraine patients completed ≥ 48 weeks of anti-CGRP mAbs treatment. Responders accounted for 60.5% (346/572), late responders for 15% (86/572), and ultra-late responders for 15.7% (90/572). Among ultra-late responders , 7.3% (42/572) maintained the ≥ 50% response rate across all subsequent time intervals (weeks 28, 32, 36, 40, 44, and 48) and were considered persistent ultra-late responders , while 8.4% (48/572) missed the ≥ 50% response rate at ≥ 1 subsequent time interval and were classified as fluctuating ultra-late responders . Fifty patients (8.7%) did not respond at any time interval ≤ 48 weeks. Ultra-late responders differed from responders for higher BMI ( p  = 0.033), longer duration of medication overuse ( p  &lt; 0.001), lower NRS ( p  = 0.017) and HIT-6 scores ( p  = 0.002), higher frequency of dopaminergic symptoms ( p  = 0.002), less common unilateral pain—either alone ( p  = 0.010) or in combination with UAS ( p  = 0.023), allodynia ( p  = 0.043), or UAS and allodynia ( p  = 0.012)—a higher number of comorbidities ( p  = 0.012), psychiatric comorbidities ( p  = 0.010) and a higher proportion of patients with ≥ 1 comorbidity ( p  = 0.020). Conclusion Two-thirds of patients not responding to anti-CGRP mAbs ≤ 24 weeks do respond later, while non-responders  ≤ 48 weeks are quite rare (8.7%). These findings suggest to rethink the duration of migraine prophylaxis and the definition of resistant and refractory migraine, currently based on the response after 2–3 months of treatment.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>38231271</pmid><doi>10.1007/s00415-023-12103-4</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-5670-3755</orcidid><oa>free_for_read</oa></addata></record>
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source Springer Nature
subjects Calcitonin
Calcitonin gene-related peptide
Comorbidity
Dopamine receptors
Headache
Medicine
Medicine & Public Health
Migraine
Monoclonal antibodies
Neurology
Neuroradiology
Neurosciences
Original Communication
Pain perception
Prophylaxis
Response rates
title Ultra-late response (> 24 weeks) to anti-CGRP monoclonal antibodies in migraine: a multicenter, prospective, observational study
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