Efficacy, tolerability, and safety of erenumab for the preventive treatment of persistent post-traumatic headache attributed to mild traumatic brain injury: an open-label study

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Efficacy, tolerability, and safety of erenumab for the preventive treatment of persistent post-traumatic headache attributed to mild traumatic brain injury : an open-label study. / Ashina, Håkan; Iljazi, Afrim; Al-Khazali, Haidar Muhsen; Eigenbrodt, Anna Kristina; Larsen, Eigil Lindekilde; Andersen, Amalie Middelboe; Hansen, Kevin John; Braüner, Karoline Bendix; Mørch-Jessen, Thomas; Chaudhry, Basit; Antic, Sonja; Christensen, Casper Emil; Ashina, Messoud; Amin, Faisal Mohammad; Schytz, Henrik Winther.

In: Journal of Headache and Pain, Vol. 21, 62, 2020.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Ashina, H, Iljazi, A, Al-Khazali, HM, Eigenbrodt, AK, Larsen, EL, Andersen, AM, Hansen, KJ, Braüner, KB, Mørch-Jessen, T, Chaudhry, B, Antic, S, Christensen, CE, Ashina, M, Amin, FM & Schytz, HW 2020, 'Efficacy, tolerability, and safety of erenumab for the preventive treatment of persistent post-traumatic headache attributed to mild traumatic brain injury: an open-label study', Journal of Headache and Pain, vol. 21, 62. https://doi.org/10.1186/s10194-020-01136-z

APA

Ashina, H., Iljazi, A., Al-Khazali, H. M., Eigenbrodt, A. K., Larsen, E. L., Andersen, A. M., Hansen, K. J., Braüner, K. B., Mørch-Jessen, T., Chaudhry, B., Antic, S., Christensen, C. E., Ashina, M., Amin, F. M., & Schytz, H. W. (2020). Efficacy, tolerability, and safety of erenumab for the preventive treatment of persistent post-traumatic headache attributed to mild traumatic brain injury: an open-label study. Journal of Headache and Pain, 21, [62]. https://doi.org/10.1186/s10194-020-01136-z

Vancouver

Ashina H, Iljazi A, Al-Khazali HM, Eigenbrodt AK, Larsen EL, Andersen AM et al. Efficacy, tolerability, and safety of erenumab for the preventive treatment of persistent post-traumatic headache attributed to mild traumatic brain injury: an open-label study. Journal of Headache and Pain. 2020;21. 62. https://doi.org/10.1186/s10194-020-01136-z

Author

Ashina, Håkan ; Iljazi, Afrim ; Al-Khazali, Haidar Muhsen ; Eigenbrodt, Anna Kristina ; Larsen, Eigil Lindekilde ; Andersen, Amalie Middelboe ; Hansen, Kevin John ; Braüner, Karoline Bendix ; Mørch-Jessen, Thomas ; Chaudhry, Basit ; Antic, Sonja ; Christensen, Casper Emil ; Ashina, Messoud ; Amin, Faisal Mohammad ; Schytz, Henrik Winther. / Efficacy, tolerability, and safety of erenumab for the preventive treatment of persistent post-traumatic headache attributed to mild traumatic brain injury : an open-label study. In: Journal of Headache and Pain. 2020 ; Vol. 21.

Bibtex

@article{2e61e23a734c47e59102c065d472ea38,
title = "Efficacy, tolerability, and safety of erenumab for the preventive treatment of persistent post-traumatic headache attributed to mild traumatic brain injury: an open-label study",
abstract = "Background: Calcitonin gene-related peptide (CGRP) has recently been implicated in the pathogenesis of post-traumatic headache (PTH), which raises the prospect for therapeutic use of monoclonal antibodies targeting CGRP or its receptor. Therefore, we decided to assess the efficacy, tolerability, and safety of erenumab for prevention of persistent PTH attributed to mild traumatic brain injury. Methods: A single-center, non-randomized, single-arm, open-label study of erenumab for adults aged 18-65 years with persistent PTH. Patients were assigned to receive 140-mg erenumab monthly by two subcutaneous 1-mL injections, given every 4 weeks for 12 weeks. The primary outcome measure was the mean change in number of monthly headache days of moderate to severe intensity from baseline (4-week pretreatment period) to week 9 through 12. Tolerability and safety endpoints were adverse events (i.e. number and type). Results: Eighty-nine of 100 patients completed the open-label trial. At baseline, the mean monthly number of headache days of moderate to severe intensity was 15.7. By week 9 through 12, the number was reduced by 2.8 days. The most common adverse events were constipation (n = 30) and injection-site reactions (n = 15). Of 100 patients who received at least one dose of erenumab, two patients discontinued the treatment regimen due to adverse events. Conclusions: Among patients with persistent PTH, erenumab resulted in a lower frequency of moderate to severe headache days in this 12-week open-label trial. In addition, erenumab was well-tolerated as discontinuations due to adverse events were low. Placebo-controlled randomized clinical trials are needed to adequately evaluate the efficacy and safety of erenumab in patients with persistent PTH. Trial registration: ClinicalTrials.Gov, NCT03974360. Registered on April 17, 2019-Retrospectively registered",
keywords = "Clinical management, Concussion, Head injury, Head trauma, Secondary headache",
author = "H{\aa}kan Ashina and Afrim Iljazi and Al-Khazali, {Haidar Muhsen} and Eigenbrodt, {Anna Kristina} and Larsen, {Eigil Lindekilde} and Andersen, {Amalie Middelboe} and Hansen, {Kevin John} and Bra{\"u}ner, {Karoline Bendix} and Thomas M{\o}rch-Jessen and Basit Chaudhry and Sonja Antic and Christensen, {Casper Emil} and Messoud Ashina and Amin, {Faisal Mohammad} and Schytz, {Henrik Winther}",
year = "2020",
doi = "10.1186/s10194-020-01136-z",
language = "English",
volume = "21",
journal = "Journal of Headache and Pain",
issn = "1129-2369",
publisher = "Springer",

}

RIS

TY - JOUR

T1 - Efficacy, tolerability, and safety of erenumab for the preventive treatment of persistent post-traumatic headache attributed to mild traumatic brain injury

T2 - an open-label study

AU - Ashina, Håkan

AU - Iljazi, Afrim

AU - Al-Khazali, Haidar Muhsen

AU - Eigenbrodt, Anna Kristina

AU - Larsen, Eigil Lindekilde

AU - Andersen, Amalie Middelboe

AU - Hansen, Kevin John

AU - Braüner, Karoline Bendix

AU - Mørch-Jessen, Thomas

AU - Chaudhry, Basit

AU - Antic, Sonja

AU - Christensen, Casper Emil

AU - Ashina, Messoud

AU - Amin, Faisal Mohammad

AU - Schytz, Henrik Winther

PY - 2020

Y1 - 2020

N2 - Background: Calcitonin gene-related peptide (CGRP) has recently been implicated in the pathogenesis of post-traumatic headache (PTH), which raises the prospect for therapeutic use of monoclonal antibodies targeting CGRP or its receptor. Therefore, we decided to assess the efficacy, tolerability, and safety of erenumab for prevention of persistent PTH attributed to mild traumatic brain injury. Methods: A single-center, non-randomized, single-arm, open-label study of erenumab for adults aged 18-65 years with persistent PTH. Patients were assigned to receive 140-mg erenumab monthly by two subcutaneous 1-mL injections, given every 4 weeks for 12 weeks. The primary outcome measure was the mean change in number of monthly headache days of moderate to severe intensity from baseline (4-week pretreatment period) to week 9 through 12. Tolerability and safety endpoints were adverse events (i.e. number and type). Results: Eighty-nine of 100 patients completed the open-label trial. At baseline, the mean monthly number of headache days of moderate to severe intensity was 15.7. By week 9 through 12, the number was reduced by 2.8 days. The most common adverse events were constipation (n = 30) and injection-site reactions (n = 15). Of 100 patients who received at least one dose of erenumab, two patients discontinued the treatment regimen due to adverse events. Conclusions: Among patients with persistent PTH, erenumab resulted in a lower frequency of moderate to severe headache days in this 12-week open-label trial. In addition, erenumab was well-tolerated as discontinuations due to adverse events were low. Placebo-controlled randomized clinical trials are needed to adequately evaluate the efficacy and safety of erenumab in patients with persistent PTH. Trial registration: ClinicalTrials.Gov, NCT03974360. Registered on April 17, 2019-Retrospectively registered

AB - Background: Calcitonin gene-related peptide (CGRP) has recently been implicated in the pathogenesis of post-traumatic headache (PTH), which raises the prospect for therapeutic use of monoclonal antibodies targeting CGRP or its receptor. Therefore, we decided to assess the efficacy, tolerability, and safety of erenumab for prevention of persistent PTH attributed to mild traumatic brain injury. Methods: A single-center, non-randomized, single-arm, open-label study of erenumab for adults aged 18-65 years with persistent PTH. Patients were assigned to receive 140-mg erenumab monthly by two subcutaneous 1-mL injections, given every 4 weeks for 12 weeks. The primary outcome measure was the mean change in number of monthly headache days of moderate to severe intensity from baseline (4-week pretreatment period) to week 9 through 12. Tolerability and safety endpoints were adverse events (i.e. number and type). Results: Eighty-nine of 100 patients completed the open-label trial. At baseline, the mean monthly number of headache days of moderate to severe intensity was 15.7. By week 9 through 12, the number was reduced by 2.8 days. The most common adverse events were constipation (n = 30) and injection-site reactions (n = 15). Of 100 patients who received at least one dose of erenumab, two patients discontinued the treatment regimen due to adverse events. Conclusions: Among patients with persistent PTH, erenumab resulted in a lower frequency of moderate to severe headache days in this 12-week open-label trial. In addition, erenumab was well-tolerated as discontinuations due to adverse events were low. Placebo-controlled randomized clinical trials are needed to adequately evaluate the efficacy and safety of erenumab in patients with persistent PTH. Trial registration: ClinicalTrials.Gov, NCT03974360. Registered on April 17, 2019-Retrospectively registered

KW - Clinical management

KW - Concussion

KW - Head injury

KW - Head trauma

KW - Secondary headache

UR - http://www.scopus.com/inward/record.url?scp=85086007958&partnerID=8YFLogxK

U2 - 10.1186/s10194-020-01136-z

DO - 10.1186/s10194-020-01136-z

M3 - Journal article

C2 - 32493206

AN - SCOPUS:85086007958

VL - 21

JO - Journal of Headache and Pain

JF - Journal of Headache and Pain

SN - 1129-2369

M1 - 62

ER -

ID: 250207137