{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T00:51:20Z","timestamp":1787014280753,"version":"build-2736575974"},"reference-count":42,"publisher":"Wiley","issue":"7","license":[{"start":{"date-parts":[[2024,6,22]],"date-time":"2024-06-22T00:00:00Z","timestamp":1719014400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"funder":[{"DOI":"10.13039\/100006483","name":"AbbVie","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100006483","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["headachejournal.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Headache"],"published-print":{"date-parts":[[2024,7]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To characterize the long\u2010term (56\u2010week) benefits of continuous onabotulinumtoxinA treatment response in individuals with chronic migraine (CM) who achieved reduction to &lt;15\u2009headache days\/month with treatment.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>There are limited data exploring reductions in monthly headache days to levels consistent with episodic migraine among those experiencing CM. Understanding the impact of sustained preventive treatment response in CM can provide important information about the impact of successful therapy.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>The two Phase 3 REsearch Evaluating Migraine Prophylaxis Therapy trials of onabotulinumtoxinA in adults included a 24\u2010week, randomized, double\u2010blind, placebo\u2010controlled phase and a 32\u2010week open\u2010label phase. Data were pooled to determine proportions of individuals with &lt;15\u2009headache days\/month while on treatment during several time periods in the double\u2010blind phase (Weeks 21\u201324; any 12 consecutive weeks; Weeks 13\u201324) and the entire study (Weeks 53\u201356; any 12 consecutive weeks; any 4\u2010week period). We assessed the long\u2010term impact on mean monthly headache days and changes from baseline on the six\u2010item Headache Impact Test (HIT\u20106) and Migraine\u2010Specific Quality of Life questionnaire version 2.1 (MSQv2.1).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      We analyzed 1384 participants with chronic migraine (double\u2010blind: onabotulinumtoxinA,\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u2009688; placebo,\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u2009696; open\u2010label:\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u2009688 [onabotulinumtoxinA]). The discontinuation rates prior to the completion of the full 56\u2010week treatment period for onabotulinumtoxinA and placebo were 25.4% (\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u2009175) and 29.3% (\n                      <jats:italic>n<\/jats:italic>\n                      \u2009=\u2009204), respectively. During Weeks 13\u201324 of the double\u2010blind phase, significantly more onabotulinumtoxinA\u2010treated (386\/688 [56.1%]) than placebo\u2010treated (342\/696 [49.1%]) individuals had &lt;15\u2009headache days\/month (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.010), with fewer monthly headache days for onabotulinumtoxinA versus placebo responders. The proportions of participants achieving &lt;15 monthly headache days with onabotulinumtoxinA were 60.9% (419\/688) at Weeks 25\u201356, 81.1% (558\/688) at Weeks 53\u201356, and 79.4% (546\/688) during any consecutive 12\u2010week period. Mean changes from baseline on the HIT\u20106 and MSQv2.1 questionnaire surpassed within\u2010group minimal important difference thresholds in all periods. At Week 24, onabotulinumtoxinA\u2010treated participants who achieved &lt;15 monthly headache days during Weeks 21\u201324 had a greater mean HIT\u20106 score reduction (\u22126.5 vs. \u22121.4) and greater mean MSQv2.1 Role\u2010Function Restrictive score improvements (21.3 vs. 6.4) than those who did not achieve &lt;15 monthly headache days during the same period.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>Participants who achieved &lt;15 monthly headache days with onabotulinumtoxinA treatment achieved meaningful benefits in headache\u2010related disability and migraine\u2010specific quality of life compared with those who remained at or above the 15\u2013monthly headache days threshold. Sustained benefits observed over 56\u2009weeks support long\u2010term onabotulinumtoxinA use for the prevention of CM.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/head.14743","type":"journal-article","created":{"date-parts":[[2024,6,22]],"date-time":"2024-06-22T03:53:33Z","timestamp":1719028413000},"page":"838-848","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":8,"title":["Sustained benefits of onabotulinumtoxinA treatment in chronic migraine: An analysis of the pooled Phase 3 REsearch Evaluating Migraine Prophylaxis Therapy (PREEMPT) randomized controlled trials"],"prefix":"10.1111","volume":"64","author":[{"given":"Stephen D.","family":"Silberstein","sequence":"first","affiliation":[{"name":"Jefferson Headache Center Thomas Jefferson University  Philadelphia Pennsylvania USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hans\u2010Christoph","family":"Diener","sequence":"additional","affiliation":[{"name":"Department of Neuroepidemiology Institute for Medical Informatics, Biometry and Epidemiology University of Duisburg\u2010Essen  Essen Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-9486-6790","authenticated-orcid":false,"given":"David W.","family":"Dodick","sequence":"additional","affiliation":[{"name":"Department of Neurology Mayo Clinic  Phoenix Arizona USA"},{"name":"Atria Academy of Science and Medicine  New York New York USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Katherine","family":"Sommer","sequence":"additional","affiliation":[{"name":"Allergan, an AbbVie Company  Irvine California USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2652-2897","authenticated-orcid":false,"given":"Richard B.","family":"Lipton","sequence":"additional","affiliation":[{"name":"Department of Neurology, Montefiore Headache Center Albert Einstein College of Medicine  Bronx New York USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2024,6,22]]},"reference":[{"key":"e_1_2_13_2_1","doi-asserted-by":"crossref","first-page":"301","DOI":"10.1177\/0333102410381145","article-title":"Disability, HRQoL and resource use among chronic and episodic migraineurs: results from the International Burden of Migraine Study (IBMS)","volume":"31","author":"Blumenfeld AM","year":"2011","journal-title":"Cephalalgia"},{"key":"e_1_2_13_3_1","doi-asserted-by":"crossref","first-page":"837","DOI":"10.1177\/0333102411398400","article-title":"Quality of life impairment, disability and economic burden associated with chronic daily headache, focusing on chronic migraine with or without medication overuse: a systematic 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