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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 |
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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 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11055785</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3047415207</sourcerecordid><originalsourceid>FETCH-LOGICAL-c475t-acd38eef7f8c6bd343f203e494150a633a2ffaf3e3e1c8b328bbf5a7809ba1763</originalsourceid><addsrcrecordid>eNp9UctuFDEQtBCILIEf4IAscQlSDH7uzHAAoRUEpEggRM6Wx9OzOMzYg-1ZlBsSJ_6Cb-FT-BK8uyE8Dpxa6qquru5C6C6jDxml1aNEqWSKUC4I44wKIq-hBZOCEyZVcx0tqJCUKKHkAbqV0jmltC7ATXQgai4Yr9gCfTkbcjRkMBlwhDQFnwAfPfnx-SuX3799AviQHuAcsPHZkdXJ2zd4DD7YIXgz7Jpt6Bwk7Dwe3Toa5-ExNnich-ws-AzxGE8xpAlsdhs4xqFNEDcmu51CynN3cRvd6M2Q4M5lPURnL56_W70kp69PXq2enRIrK5WJsZ2oAfqqr-2y7YQUPacCZFOeQM1SCMP73vQCBDBbt4LXbdsrU9W0aQ2rluIQPd3rTnM7Qre1F82gp-hGEy90ME7_jXj3Xq_DRjNGlapqVRSOLhVi-DhDynp0ycIwGA9hTpo3TDV1w9h22f1_qOdhjuXmpAWVVfHMaVVYfM-y5UcpQn_lhlG9DVnvQ9YlZL0LWcsydO_PO65GfqVaCGJPSAXya4i_d_9H9ifXibYH</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3047415207</pqid></control><display><type>article</type><title>Ultra-late response (> 24 weeks) to anti-CGRP monoclonal antibodies in migraine: a multicenter, prospective, observational study</title><source>Springer Nature</source><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</creator><creatorcontrib>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 ; ERT; for the Italian Migraine Registry study group ; ERT; for the Italian Migraine Registry study group</creatorcontrib><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
< 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 & 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 (> 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 > 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
< 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 & 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 (> 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 & 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; for the Italian Migraine Registry study group</creatorcontrib><creatorcontrib>ERT; for the Italian Migraine Registry study group</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Barbanti, Piero</au><au>Aurilia, Cinzia</au><au>Egeo, Gabriella</au><au>Proietti, Stefania</au><au>D’Onofrio, Florindo</au><au>Torelli, Paola</au><au>Aguggia, Marco</au><au>Bertuzzo, Davide</au><au>Finocchi, Cinzia</au><au>Trimboli, Michele</au><au>Cevoli, Sabina</au><au>Fiorentini, Giulia</au><au>Orlando, Bianca</au><au>Zucco, Maurizio</au><au>Di Clemente, Laura</au><au>Cetta, Ilaria</au><au>Colombo, Bruno</au><au>di Poggio, Monica Laura Bandettini</au><au>Favoni, Valentina</au><au>Grazzi, Licia</au><au>Salerno, Antonio</au><au>Carnevale, Antonio</au><au>Robotti, Micaela</au><au>Frediani, Fabio</au><au>Altamura, Claudia</au><au>Filippi, Massimo</au><au>Vernieri, Fabrizio</au><au>Bonassi, Stefano</au><aucorp>ERT; 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 (> 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 > 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
< 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> |
fulltext | fulltext |
identifier | ISSN: 0340-5354 |
ispartof | Journal of neurology, 2024-05, Vol.271 (5), p.2434-2443 |
issn | 0340-5354 1432-1459 1432-1459 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11055785 |
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 |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T03%3A55%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ultra-late%20response%20(%3E%E2%80%8924%C2%A0weeks)%20to%20anti-CGRP%20monoclonal%20antibodies%20in%20migraine:%20a%20multicenter,%20prospective,%20observational%20study&rft.jtitle=Journal%20of%20neurology&rft.au=Barbanti,%20Piero&rft.aucorp=ERT;%20for%20the%20Italian%20Migraine%20Registry%20study%20group&rft.date=2024-05-01&rft.volume=271&rft.issue=5&rft.spage=2434&rft.epage=2443&rft.pages=2434-2443&rft.issn=0340-5354&rft.eissn=1432-1459&rft_id=info:doi/10.1007/s00415-023-12103-4&rft_dat=%3Cproquest_pubme%3E3047415207%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c475t-acd38eef7f8c6bd343f203e494150a633a2ffaf3e3e1c8b328bbf5a7809ba1763%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3047415207&rft_id=info:pmid/38231271&rfr_iscdi=true |