Evidence map›Paper›PMID 33880725›Full record

ReviewPain and therapy2021

Real-World Evidence for Control of Chronic Migraine Patients Receiving CGRP Monoclonal Antibody Therapy Added to OnabotulinumtoxinA: A Retrospective Chart Review.

Andrew M Blumenfeld, Benjamin M Frishberg, Jack D Schim, Ashley Iannone, Gary Schneider, Larisa Yedigarova, Aubrey Manack Adams

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Pain and therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05724771 (Assessing the Safety and Efficacy of Utilizing CGRPmAb Fremanezumab), which is not on this map. Cited by 52 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 3 pooled it
13.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05724771 phase4active not recruitingnot on this mapstarted 2023, after this paper: background citation

Assessing the Safety and Efficacy of Utilizing CGRPmAb Fremanezumab (Ajovy) in Chronic Migraine Patients Currently on Monotherapy OnabotulinumtoxinA (Botox).

TypeinterventionalSponsorChicago Headache Center & Research InstituteRan2023 to 2025Enrolled50ConditionsChronic Migraine, HeadacheArmsCombination of Botox + CGRPmAb (Fremanezumab 225mg/1.5mL)
3 · Its place in the literature

Who cites it

52 citing papers in PubMed, 3 syntheses or guidelines pooled it, 98 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Andrew M BlumenfeldHeadache Center of Southern California, The Neurology Center, 6010 Hidden Valley Road, Suite 200, Carlsbad, CA, 92011, USA. blumenfeld@neurocenter.com.
Benjamin M FrishbergHeadache Center of Southern California, The Neurology Center, 6010 Hidden Valley Road, Suite 200, Carlsbad, CA, 92011, USA.
Jack D SchimHeadache Center of Southern California, The Neurology Center, 6010 Hidden Valley Road, Suite 200, Carlsbad, CA, 92011, USA.
Ashley IannoneICON Plc, Boston, MA, USA.
Gary SchneiderICON Plc, Boston, MA, USA.
Larisa YedigarovaAllergan, an AbbVie Company, Irvine, CA, USA.
Aubrey Manack AdamsAllergan, an AbbVie Company, Irvine, CA, USA.
Neurology Center of Southern California · USAbbVie (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCombination use of onabotulinumtoxinA and calcitonin gene-related peptide (CGRP) monoclonal antibodies (mAbs) has the potential to be more effective than either therapy alone for migraine prevention.

methodsThis retrospective, longitudinal chart review included adults with chronic migraine treated at one clinical site with ≥ 2 consecutive cycles of onabotulinumtoxinA and ≥ 1 month of subsequent combination treatment with CGRP mAbs. Charts at time of mAb prescription (baseline) and up to four visits ~ 3, 6, 9, and 12 months post-baseline were reviewed for safety, tolerability, and outcome measures (monthly headache days [MHDs], headache intensity, and migraine-related disability [MIDAS]).

resultsOf 300 charts reviewed, 257 patients met eligibility criteria (mean age: 50 years; 82% women). Average headache frequency was 21.5 MHDs before initiation of onabotulinumtoxinA and 12.1 MHDs before adding CGRP mAb therapy. Prescribed mAbs were erenumab (78%), fremanezumab (6%), and galcanezumab (16%). Over the entire study, patients discontinued CGRP mAb more frequently than onabotulinumtoxinA (23 vs. 3%). Adverse events occurred in 28% of patients, most commonly constipation (9%). Compared with onabotulinumtoxinA alone (baseline), MHDs decreased significantly at all visits (mean decrease: 3.5-4.0 MHDs over ~ 6-12 months of combination treatment); 45.1% of patients had clinically meaningful improvement in migraine-related disability (≥ 5-point reduction in MIDAS score) after ~ 6 months.

conclusionsIn this real-world study, combination treatment with onabotulinumtoxinA and CGRP mAbs was well tolerated, with no new safety signals identified, and was associated with additional clinically meaningful benefits. More real-world and controlled trials should be considered to further assess safety and potential benefits of combination treatment. Video abstract: Real-world data suggests that CGRP inhibitors improve onabotulinumtoxinA efficacy for chronic migraine (MP4 20,067 kb).

Indexed as

CGRP receptorChronic daily headacheChronic headacheCombination therapyMigraine headachePreventive treatmentType A botulinum toxins

Identifiers

PMID33880725
PMCPMC8586140
OpenAlexW3154454412

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.