Comparing the relative and absolute effect of erenumab: is a 50% response enough? Results from the ESTEEMen study

. 2022 Mar 19 ; 23 (1) : 38. [epub] 20220319

Jazyk angličtina Země Anglie, Velká Británie Médium electronic

Typ dokumentu srovnávací studie, časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid35305579
Odkazy

PubMed 35305579
PubMed Central PMC8933935
DOI 10.1186/s10194-022-01408-w
PII: 10.1186/s10194-022-01408-w
Knihovny.cz E-zdroje

BACKGROUND: Monoclonal antibodies acting on the calcitonin gene-related peptide (CGRP) or its receptor have changed migraine preventive treatment. Those treatments have led to reconsidering the outcomes of migraine prevention. Available data mostly considered benefits in terms of relative efficacy (percent or absolute decrease in monthly migraine days [MMDs] or headache days compared with baseline). However, not enough attention has been paid to residual MMDs and/or migraine-related disability in treated patients. In the present study, we aimed at comparing the relative and absolute efficacy of erenumab. METHODS: ESTEEMen was a collaborative project among 16 European headache centers which already performed real-life data collections on patients treated with erenumab for at least 12 weeks. For the present study, we performed a subgroup analysis on patients with complete data on MMDs at baseline and at weeks 9-12 of treatment. Starting from efficacy thresholds proposed by previous literature, we classified patients into 0-29%, 30-49%, 50-74%, and ≥75% responders according to MMD decrease from baseline to weeks 9-12 of treatment. For each response category, we reported the median MMDs and Headache Impact test-6 (HIT-6) scores at baseline and at weeks 9-12. We categorized the number of residual MMDs at weeks 9-12 as follows: 0-3, 4-7, 8-14, ≥15. We classified HIT-6 score into four categories: ≤49, 50-55, 56-59, and ≥60. To keep in line with the original scope of the ESTEEMen study, calculations were performed in men and women. RESULTS: Out of 1215 patients, at weeks 9-12, 381 (31.4%) had a 0-29% response, 186 (15.3%) a 30-49% response, 396 (32.6%) a 50-74% response, and 252 (20.7%) a ≥75% response; 246 patients (20.2%) had 0-3 residual MMDs, 443 (36.5%) had 4-7 MMDs, 299 (24.6%) had 8-14 MMDs, and 227 (18.7%) had ≥15 MMDs. Among patients with 50-74% response, 246 (62.1%) had 4-7 and 94 (23.7%) 8-14 residual MMDs, while among patients with ≥75% response 187 (74.2%) had 0-3 and 65 (25.8%) had 4-7 residual MMDs. CONCLUSIONS: The present study shows that even patients with good relative response to erenumab may have a clinically non-negligible residual migraine burden. Relative measures of efficacy cannot be enough to thoroughly consider the efficacy of migraine prevention.

Department of Neurology Alfred Health Melbourne VIC Australia

Department of Neurology Charité Universitätsmedizin Berlin Berlin Germany

Department of Neurology F Renzetti Hospital Lanciano Chieti Italy

Department of Neurology G Mazzini Hospital Teramo Italy

Department of Neurology S Pio da Pietrelcina Hospital Vasto Chieti Italy

Department of Neurology West German Headache Center University hospital Essen Essen Germany

Headache and Neurosonology Unit Fondazione Policlinico Universitario Campus Bio Medico Rome Italy

Headache and Pain Unit IRCCS San Raffaele Rome Italy

Headache Center Department of Medical Surgical Neurological Metabolic and Aging Sciences University of Campania Luigi Vanvitelli Naples Italy

Headache Center Geriatrics Clinic Department of Medicine and Science of Aging and Center for Advanced Studies and Technology G D'Annunzio University Chieti Italy

Headache Centre Division of Neurology and Stroke Unit A Cardarelli Hospital Naples Italy

Headache Centre Ospedale S Antonio Abate ASST Valle Olona Gallarate Italy

IRCCS Istituto delle Scienze Neurologiche di Bologna Bologna Italy

Medical toxicology Headache and Drug Abuse Research Center; Department of biomedical metabolic and neural sciences University of Modena and Reggio Emilia Modena Italy

Military University Hospital Prague Department of Neurology 1st Faculty of Medicine Charles University Prague Czech Republic

Motol University Hospital Prague Department of Neurology 2nd Faculty of Medicine Charles University Prague Czech Republic

Neuroscience Section Department of Applied Clinical Sciences and Biotechnology University of L'Aquila Via Vetoio 1 L'Aquila Italy

PhD school in neurosciences; Department of biomedical metabolic and neural sciences University of Modena and Reggio Emilia Modena Italy

Private Practice Essen Germany

San Raffaele University Rome Italy

Sechenov 1st Moscow State Medical University Moscow Russian Federation

Southwest Neurology Audit and Research group Department of Neurology Derriford Hospital Plymouth PL6 8DH UK

The Headache Service Guy's and St Thomas' NHS Foundation Trust Westminster Bridge Road London SE1 7EH UK

Universitätsmedizin Greifswald Greifswald Germany

Zobrazit více v PubMed

Edvinsson L. CGRP Antibodies as Prophylaxis in Migraine. Cell. 2018;175(7):1719. doi: 10.1016/j.cell.2018.11.049. PubMed DOI

Edvinsson L, Haanes KA, Warfvinge K, Krause DN. CGRP as the target of new migraine therapies - successful translation from bench to clinic. Nat Rev Neurol. 2018;14(6):338–350. doi: 10.1038/s41582-018-0003-1. PubMed DOI

Goadsby PJ, Reuter U, Hallstrom Y, Broessner G, Bonner JH, Zhang F, et al. A Controlled Trial of Erenumab for Episodic Migraine. N Engl J Med. 2017;377(22):2123–2132. doi: 10.1056/NEJMoa1705848. PubMed DOI

Reuter U, Goadsby PJ, Lanteri-Minet M, Wen S, Hours-Zesiger P, Ferrari MD, et al. Efficacy and tolerability of erenumab in patients with episodic migraine in whom two-to-four previous preventive treatments were unsuccessful: a randomised, double-blind, placebo-controlled, phase 3b study. Lancet. 2018;392(10161):2280–2287. doi: 10.1016/S0140-6736(18)32534-0. PubMed DOI

Tepper S, Ashina M, Reuter U, Brandes JL, Dolezil D, Silberstein S, et al. Safety and efficacy of erenumab for preventive treatment of chronic migraine: a randomised, double-blind, placebo-controlled phase 2 trial. Lancet Neurol. 2017;16(6):425–434. doi: 10.1016/S1474-4422(17)30083-2. PubMed DOI

Barbanti P, Aurilia C, Egeo G, Fofi L, Cevoli S, Colombo B, et al. Erenumab in the prevention of high-frequency episodic and chronic migraine: Erenumab in Real Life in Italy (EARLY), the first Italian multicenter, prospective real-life study. Headache. 2021;61(2):363–372. doi: 10.1111/head.14032. PubMed DOI

Cheng S, Jenkins B, Limberg N, Hutton E. Erenumab in Chronic Migraine: An Australian Experience. Headache. 2020;60(10):2555–2562. doi: 10.1111/head.13968. PubMed DOI

Lambru G, Hill B, Murphy M, Tylova I, Andreou AP. A prospective real-world analysis of erenumab in refractory chronic migraine. J Headache Pain. 2020;21(1):61. doi: 10.1186/s10194-020-01127-0. PubMed DOI PMC

Ornello R, Casalena A, Frattale I, Gabriele A, Affaitati G, Giamberardino MA, et al. Real-life data on the efficacy and safety of erenumab in the Abruzzo region, central Italy. J Headache Pain. 2020;21(1):32. doi: 10.1186/s10194-020-01102-9. PubMed DOI PMC

Raffaelli B, Kalantzis R, Mecklenburg J, Overeem LH, Neeb L, Gendolla A, et al. Erenumab in Chronic Migraine Patients Who Previously Failed Five First-Line Oral Prophylactics and OnabotulinumtoxinA: A Dual-Center Retrospective Observational Study. Front Neurol. 2020;11:417. doi: 10.3389/fneur.2020.00417. PubMed DOI PMC

Ranieri A, Alfieri G, Napolitano M, Servillo G, Candelaresi P, Di Iorio W, et al. One year experience with erenumab: real-life data in 30 consecutive patients. Neurol Sci. 2020;41(Suppl 2):505–506. doi: 10.1007/s10072-020-04677-y. PubMed DOI

Russo A, Silvestro M, Scotto di Clemente F, Trojsi F, Bisecco A, Bonavita S, et al. Multidimensional assessment of the effects of erenumab in chronic migraine patients with previous unsuccessful preventive treatments: a comprehensive real-world experience. J Headache Pain. 2020;21(1):69. doi: 10.1186/s10194-020-01143-0. PubMed DOI PMC

Scheffler A, Messel O, Wurthmann S, Nsaka M, Kleinschnitz C, Glas M, et al. Erenumab in highly therapy-refractory migraine patients: First German real-world evidence. J Headache Pain. 2020;21(1):84. doi: 10.1186/s10194-020-01151-0. PubMed DOI PMC

Talbot J, Stuckey R, Crawford L, Weatherby S, Mullin S. Improvements in pain, medication use and quality of life in onabotulinumtoxinA-resistant chronic migraine patients following erenumab treatment - real world outcomes. J Headache Pain. 2021;22(1):5. doi: 10.1186/s10194-020-01214-2. PubMed DOI PMC

Valle ED, Di Falco M, Mancioli A, Corbetta S, La Spina I. Efficacy and safety of erenumab in the real-life setting of S. Antonio Abate Hospital's Headache Center (Gallarate) Neurol Sci. 2020;41(Suppl:2):465. PubMed

Khalil M, Zafar HW, Quarshie V, Ahmed F (2014) Prospective analysis of the use of OnabotulinumtoxinA (BOTOX) in the treatment of chronic migraine; real-life data in 254 patients from Hull, U.K. J Headache Pain. 15(54) PubMed PMC

(2018) Headache Classification Committee of the International Headache Society (IHS) The International Classification of Headache Disorders, 3rd edition. Cephalalgia. 38(1):1-211. PubMed

Sacco S, Braschinsky M, Ducros A, Lampl C, Little P, van den Brink AM, et al. European headache federation consensus on the definition of resistant and refractory migraine : Developed with the endorsement of the European Migraine & Headache Alliance (EMHA) J Headache Pain. 2020;21(1):76. doi: 10.1186/s10194-020-01130-5. PubMed DOI PMC

Ornello R, Baraldi C, Guerzoni S, al. e, Collaborators obotE (2021) Gender Differences in 3-Month Outcomes of Erenumab Treatment—Study on Efficacy and Safety of Treatment With Erenumab in Men. Front Neurol. PubMed PMC

Bayliss M, Bathenhorst AS. The HIT-6(TM): a user's guide. Lincoln, RI: QualityMetric, Inc.; 2002.

Brandes JL, Diener HC, Dolezil D, Freeman MC, McAllister PJ, Winner P, et al. The spectrum of response to erenumab in patients with chronic migraine and subgroup analysis of patients achieving >/=50%, >/=75%, and 100% response. Cephalalgia. 2020;40(1):28–38. doi: 10.1177/0333102419894559. PubMed DOI

Broessner G, Reuter U, Bonner JH, Dodick DW, Hallstrom Y, Picard H, et al. The Spectrum of Response to Erenumab in Patients With Episodic Migraine and Subgroup Analysis of Patients Achieving >/=50%, >/=75%, and 100% Response. Headache. 2020;60(9):2026–2040. doi: 10.1111/head.13929. PubMed DOI PMC

Tfelt-Hansen P, Diener HC, Steiner TJ. Problematic presentation and use of efficacy measures in current trials of CGRP monoclonal antibodies for episodic migraine prevention: A mini-review. Cephalalgia. 2020;40(1):122–126. doi: 10.1177/0333102419877663. PubMed DOI

Ashina M, Goadsby PJ, Reuter U, Silberstein S, Dodick DW, Xue F, et al. Long-term efficacy and safety of erenumab in migraine prevention: Results from a 5-year, open-label treatment phase of a randomized clinical trial. Eur J Neurol. 2021;28(5):1716–1725. doi: 10.1111/ene.14715. PubMed DOI PMC

Martelletti P, Schwedt TJ, Lanteri-Minet M, Quintana R, Carboni V, Diener HC, et al. My Migraine Voice survey: a global study of disease burden among individuals with migraine for whom preventive treatments have failed. J Headache Pain. 2018;19(1):115. doi: 10.1186/s10194-018-0946-z. PubMed DOI PMC

Sacco S, Lampl C, Maassen van den Brink A, Caponnetto V, Braschinsky M, Ducros A, et al. Burden and attitude to resistant and refractory migraine: a survey from the European Headache Federation with the endorsement of the European Migraine & Headache Alliance. J Headache Pain. 2021;22(1):39. doi: 10.1186/s10194-021-01252-4. PubMed DOI PMC

Armanious M, Khalil N, Lu Y, Jimenez-Sanders R. Erenumab and OnabotulinumtoxinA Combination Therapy for the Prevention of Intractable Chronic Migraine without Aura: A Retrospective Analysis. J Pain Palliat Care Pharmacother. 2021;35(1):1–6. doi: 10.1080/15360288.2020.1829249. PubMed DOI

Blumenfeld AM, Frishberg BM, Schim JD, Iannone A, Schneider G, Yedigarova L, et al. Real-World Evidence for Control of Chronic Migraine Patients Receiving CGRP Monoclonal Antibody Therapy Added to OnabotulinumtoxinA: A Retrospective Chart Review. Pain Ther. 2021;10(2):809–826. doi: 10.1007/s40122-021-00264-x. PubMed DOI PMC

Cohen F, Armand C, Lipton RB, Vollbracht S. Efficacy and Tolerability of Calcitonin Gene-Related Peptide-Targeted Monoclonal Antibody Medications as Add-on Therapy to OnabotulinumtoxinA in Patients with Chronic Migraine. Pain medicine (Malden, Mass). 2021;22(8):1857–1863. doi: 10.1093/pm/pnab093. PubMed DOI

Silvestro M, Tessitore A, Scotto di Clemente F, Battista G, Tedeschi G, Russo A. Additive Interaction Between Onabotulinumtoxin-A and Erenumab in Patients With Refractory Migraine. Front Neurol. 2021;12:656294. doi: 10.3389/fneur.2021.656294. PubMed DOI PMC

Toni T, Tamanaha R, Newman B, Liang Y, Lee J, Carrazana E, et al. Effectiveness of dual migraine therapy with CGRP inhibitors and onabotulinumtoxinA injections: case series. Neurol Sci. 2021;42(12):5373–5376. doi: 10.1007/s10072-021-05547-x. PubMed DOI

Sacco S, Russo A, Geppetti P, Grazzi L, Negro A, Tassorelli C, et al. What is changing in chronic migraine treatment? An algorithm for onabotulinumtoxinA treatment by the Italian chronic migraine group. Expert Rev Neurother. 2020;20(12):1275–1286. doi: 10.1080/14737175.2020.1825077. PubMed DOI

Najít záznam

Citační ukazatele

Nahrávání dat ...

    Možnosti archivace