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  <controlfield tag="005">20260116002211.0</controlfield>
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    <subfield code="2">doi</subfield>
    <subfield code="a">10.1186/s10194-025-02239-1</subfield>
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    <subfield code="2">sideral</subfield>
    <subfield code="a">147440</subfield>
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  <datafield tag="037" ind1=" " ind2=" ">
    <subfield code="a">ART-2025-147440</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Muñoz-Vendrell, Albert</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Atogepant after anti-CGRP monoclonal antibodies failure in migraine: a multicenter real-world study of effectiveness, safety, persistence and predictors of response</subfield>
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  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2025</subfield>
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    <subfield code="a">Background Atogepant is approved for migraine prevention and has shown strong efficacy in clinical trials. However, its effectiveness following failure of anti-CGRP monoclonal antibodies (MAbs) has not been evaluated in large real-world populations. Methods This multicenter observational study conducted across Spanish headache units included adults with migraine who initiated atogepant after failure of ≥1 anti-CGRP MAb and had≥3 months of follow-up. Baseline demographic and clinical variables were collected prospectively, with follow-up assessments at months 3 and 6. The primary outcome was the proportion of patients achieving a≥50% reduction in monthly migraine days (MMD) at three months. Secondary outcomes included≥30%, ≥75%, and 100% response rates; changes in headache days, pain intensity, acute medication use, and patient-reported outcomes; adverse events; treatment persistence; and factors associated with response. Results A total of 252 patients were included (mean age 48.9±12 years; 83.3% female; 80.6% with chronic migraine; 45.6% with continuous daily headache). Prior to atogepant, 39.7% had failed one anti-CGRP MAb, 27.0% two, 20.2% three, and 13.1% four. Median baseline MMD was 16, monthly headache days 27, and acute medication days 20. At 3 months, 44.4% achieved a≥30% reduction in MMD, 29.7% ≥50%, and 11.7% ≥75%. Adverse events were reported in 52.5% of patients, most commonly constipation (30%) and nausea (25%). At three months, 26.2% had discontinued treatment (65.1% due to inefficacy, 28.8% due to intolerance). Treatment persistence at 180 days was 61% (95% CI 54 to 69%). A higher number of previously failed MAbs was independently associated with reduced odds of ≥50% response (RR 0.79, 95% CI 0.64 to 0.97). Moreover, a higher number of previously failed MAbs was associated with diminished improvements across multiple clinical endpoints, including headache frequency, intensity, acute medication use, and disability measures. Conclusion Atogepant may represent a viable treatment option for patients with migraine who have failed antiCGRP MAbs. In this large real-world cohort, approximately one-third of patients achieved a≥50% response, despite a
treatment-refractory profile. However, the likelihood of response decreases with a higher number of previously failed MAbs, and mild adverse events are frequent.</subfield>
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    <subfield code="a">Access copy available to the general public</subfield>
    <subfield code="f">Unrestricted</subfield>
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    <subfield code="9">info:eu-repo/semantics/openAccess</subfield>
    <subfield code="a">by</subfield>
    <subfield code="u">https://creativecommons.org/licenses/by/4.0/deed.es</subfield>
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    <subfield code="a">info:eu-repo/semantics/article</subfield>
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    <subfield code="a">Campoy-Díaz, Sergio</subfield>
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    <subfield code="a">Valín-Villanueva, Paloma</subfield>
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    <subfield code="a">Casas-Limón, Javier</subfield>
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    <subfield code="a">Fernández-Lázaro, Iris</subfield>
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    <subfield code="a">González-García, Nuria</subfield>
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    <subfield code="a">Santos-Lasaosa, Sonia</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-5139-6031</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">González Osorio, Yésica</subfield>
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    <subfield code="a">Gonzalez-Martinez, Alicia</subfield>
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    <subfield code="a">Campdelacreu, Jaume</subfield>
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    <subfield code="a">Portocarrero-Sánchez, Leonardo</subfield>
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    <subfield code="a">Cano Sánchez, Luis Miguel</subfield>
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    <subfield code="a">García Sánchez, Sonia María</subfield>
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    <subfield code="a">Pérez-de-la-parte, Alba</subfield>
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    <subfield code="a">Morollón Sánchez-Mateos, Noemí</subfield>
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    <subfield code="a">López-Bravo, Alba</subfield>
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    <subfield code="a">Sánchez-Soblechero, Antonio</subfield>
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    <subfield code="a">Lozano Ros, Alberto</subfield>
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    <subfield code="a">Morales Hernández, Cristian</subfield>
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    <subfield code="a">Andrés López, Alberto</subfield>
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    <subfield code="a">Layos-Romero, Almudena</subfield>
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    <subfield code="a">Caronna, Edoardo</subfield>
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    <subfield code="a">Torres-Ferrús, Marta</subfield>
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    <subfield code="a">Alpuente, Alicia</subfield>
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    <subfield code="a">Pozo-Rosich, Patricia</subfield>
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    <subfield code="a">Belvís, Robert</subfield>
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    <subfield code="a">Garcia-Azorin, David</subfield>
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    <subfield code="a">Díaz-de-Terán, Javier</subfield>
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    <subfield code="a">Guerrero-Peral, Ángel Luis</subfield>
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    <subfield code="a">Gago-Veiga, Ana Beatriz</subfield>
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    <subfield code="a">Huerta-Villanueva, Mariano</subfield>
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    <subfield code="1">1007</subfield>
    <subfield code="2">610</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Medicina, Psiqu. y Derm.</subfield>
    <subfield code="c">Area Medicina</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">27, 2 (2025), [12 pp.]</subfield>
    <subfield code="p">J. headache pain</subfield>
    <subfield code="t">The Journal of headache and pain</subfield>
    <subfield code="x">1129-2369</subfield>
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