AI Article Synopsis

  • Cardiovascular adverse events (CVAEs) are a significant concern for patients undergoing Carfilzomib (CFZ) therapy for multiple myeloma (MM), but there are no established protocols for assessing cardiovascular risk.* -
  • A study evaluated the European Myeloma Network (EMN) protocol to identify key predictors of CVAEs in 116 MM patients, which included baseline assessments like blood pressure and echocardiography.* -
  • The study found five significant predictors of CVAEs and developed a risk score that successfully classified patients into low- and high-risk groups, with 44.9% experiencing CVAEs, highlighting the need for a targeted management approach.*

Article Abstract

Cardiovascular adverse events (CVAEs) are linked to Carfilzomib (CFZ) therapy in multiple myeloma (MM); however, no validated protocols on cardiovascular risk assessment are available. In this prospective study, the effectiveness of the European Myeloma Network protocol (EMN) in cardiovascular risk assessment was investigated, identifying major predictors of CVAEs. From January 2015 to March 2020, 116 MM patients who had indication for CFZ therapy underwent a baseline evaluation (including blood pressure measurements, echocardiography and arterial stiffness estimation) and were prospectively followed. The median age was 64.53 ± 8.42 years old, 56% male. Five baseline independent predictors of CVAEs were identified: office systolic blood pressure, 24-h blood pressure variability, left ventricular hypertrophy, pulse wave velocity value and global longitudinal strain. The resulting 'CVAEs risk score' distinguished a low- and a high-risk group, obtaining a negative predicting value for the high-risk group of 90%. 52 patients (44.9%) experienced one or more CVAEs: 17 (14.7%) had major and 45 (38.7%) had hypertension-related events. In conclusion, CVAEs are frequent and a specific management protocol is crucial. The EMN protocol and the risk score proved to be useful to estimate the baseline risk for CVAEs during CFZ therapy, allowing the identification of higher-risk patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8036868PMC
http://dx.doi.org/10.3390/cancers13071631DOI Listing

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