Mavacamten in the Treatment of Obstructive Hypertrophic Cardiomyopathy: from Pathophysiology To Real World Data
Randomized trials have shown that mavacamten significantly reduces left ventricular outflow tract gradients, improves symptoms and exercise capacity, and induces structural reverse remodeling with a favorable safety profile. Real-world data confirm these benefits in broader patient populations. Pharmacogenetic variability, titration protocols, and cost-effectiveness analyses have further refined its clinical use. Mavacamten represents a paradigm shift in oHCM treatment by targeting disease at its sarcomeric origin. Its integration into routine care is expanding, supported by real-world evidence. Ongoing studies will clarify its role in non-obstructive HCM, heart failure with preserved ejection fraction, pediatric populations, and early-stage disease.
Authors
- Manuel Garofalo (ORCID: https://orcid.org/0009-0007-6011-0710)
- Giorgia Panichella (ORCID: https://orcid.org/0000-0002-9049-5320)
- Mattia Zampieri (ORCID: https://orcid.org/0000-0002-1140-134X)
- Maurizio Pieroni (ORCID: https://orcid.org/0000-0002-6830-4292)
- Iacopo Olivotto
- Francesco Cappelli (ORCID: https://orcid.org/0000-0002-1622-0732)
- Angela Ilaria Fanizzi
- M Ragagnin
- Annamaria Del Franco
Institutions
- Meyer Children's Hospital (IT)
- Azienda Ospedaliero-Universitaria Careggi (IT)
- University of Florence (IT)
Publication Details
- Journal
- Current Cardiology Reports
- Published
- 2025-12-01
- DOI
- https://doi.org/10.1007/s11886-025-02316-6
- Citations
- 1
- Primary Topic
- Cardiomyopathy and Myosin Studies
- Type
- article
- Field-Weighted Citation Impact
- 1.39