Evidence map›Paper›PMID 39206723›Full record

ReviewJournal of the American Heart Association2024

Mavacamten for Obstructive Hypertrophic Cardiomyopathy: Rationale for Clinically Guided Dose Titration to Optimize Individual Response.

Anjali T Owens, Milind Desai, Matthew T Wheeler, Anna Rodonski, Samira Merali, Amy J Sehnert, Sara Saberi

Abstract readReview
In one paragraph

Review in Journal of the American Heart Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
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  7. Article
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  9. Article
  10. Corticosteroids reduce pacemaker implantation after alcohol septal ablation in oHCM patients.Clinical research in cardiology : official journal of the German Cardiac Society · 2025
    Article
  11. A FRET assay to monitor different structural states of human β-cardiac myosin including the interacting-heads motif.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Article
  13. Article
  14. Review
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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.

Anjali T OwensUniversity of Pennsylvania Perelman School of Medicine Philadelphia PA USA.ORCID 0000-0002-9669-8495
Milind DesaiHeart, Vascular, and Thoracic Institute Cleveland Clinic Cleveland OH USA.ORCID 0000-0003-0010-9797
Matthew T WheelerDivision of Cardiovascular Medicine Stanford University School of Medicine Stanford CA USA.ORCID 0000-0001-8721-3022
Anna RodonskiAscension Saint Thomas Heart West Nashville TN USA.
Samira MeraliBristol Myers Squibb Princeton NJ USA.ORCID 0000-0001-6659-3687
Amy J SehnertBristol Myers Squibb Princeton NJ USA.ORCID 0000-0003-1912-1710
Sara SaberiDivision of Cardiovascular Medicine University of Michigan Ann Arbor MI USA.ORCID 0000-0003-4473-6725

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mavacamten is the first and only cardiac myosin inhibitor approved in 5 continents for the treatment of adults with symptomatic New York Heart Association class II and III obstructive hypertrophic cardiomyopathy. An evidence-based rationale was used to develop individualized mavacamten dosing, guided by commonly used clinical parameters. Echocardiography is recommended as part of routine clinical assessment of patients with hypertrophic cardiomyopathy, and left ventricular (LV) outflow tract gradient and LV ejection fraction are parameters that can be readily assessed and monitored by echocardiography. Therefore, an echocardiography-based, clinically guided dose-titration strategy was developed to optimize patient benefit from mavacamten for the treatment of symptomatic obstructive hypertrophic cardiomyopathy while minimizing the risk of LV ejection fraction reduction. Results from clinical trials paired with extensive modeling and simulation analyses support a dose-titration and monitoring strategy based on serial echocardiographic measures of Valsalva LV outflow tract gradient and LV ejection fraction. This dosing approach allows for the identification of the lowest individualized mavacamten dose and exposure required to provide improvements in LV outflow tract obstruction, functional capacity, and symptoms. Mavacamten is primarily metabolized by CYP2C19 (cytochrome P450 2C19), and CYP2C19 metabolizer phenotype has an effect on mavacamten exposure. Therefore, this approach has also been demonstrated to provide a favorable safety profile irrespective of patients' CYP2C19 metabolizer status. The dose-titration strategy includes additional considerations for the potential onset of systolic dysfunction in the context of intercurrent illness, and for the potential of drug-drug interactions with inhibitors and substrates of cytochrome P450 enzymes. This posology is reflected in the mavacamten US prescribing information.

Indexed as

Cardiomyopathy, HypertrophicBenzylaminesCytochrome P-450 CYP2C19Dose-Response Relationship, DrugEchocardiographyHumansStroke VolumeTreatment OutcomeUracilVentricular Function, LeftBenzylaminesCYP2C19 protein, humanCytochrome P-450 CYP2C19MYK-461Uracilechocardiogramindividualized dosingleft ventricular ejection fractionleft ventricular outflow tract gradientmavacamtenobstructive hypertrophic cardiomyopathy

Identifiers

PMID39206723
PMCPMC11646538

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Registered trials

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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.