# Carfilzomib in multiple myeloma: unraveling cardiac toxicities - from mechanisms to diagnosis and management

**Authors:** Yi Gao, Di Zhou, Xue Bai, Yunjie Wang, Chenchen Wang, Lintao Bi

PMC · DOI: 10.3389/fphar.2025.1570017 · Frontiers in Pharmacology · 2025-03-27

## TL;DR

This paper reviews carfilzomib's use in treating multiple myeloma and explores its cardiovascular side effects and management.

## Contribution

The paper provides a detailed overview of carfilzomib's cardiotoxic mechanisms and management strategies.

## Key findings

- Carfilzomib causes heart failure, hypertension, arrhythmia, and ischemic heart disease.
- Recommendations are provided for evaluating and managing cardiac events during treatment.

## Abstract

The survival rates of patients with hematological malignancies such as multiple myeloma have improved with advances in cancer treatment. However, the risk of cardiovascular disease associated with novel therapeutic agents, including proteasome inhibitors (PIs), is becoming increasingly evident. PIs act on proteasome peptidases, leading to cell cycle arrest or apoptosis. Carfilzomib (CFZ), an intravenously administered irreversible PI, exhibits pronounced cardiovascular toxicity that is characterized by heart failure, hypertension, arrhythmia, and ischemic heart disease (IHD). This review focuses on CFZ, details its applications in treating multiple myeloma, presents its potential mechanisms of cardiotoxicity and the incidence of cardiotoxic events, and provides recommendations for the evaluation and management of adverse cardiac events during the early treatment of patients with this drug.

## Linked entities

- **Chemicals:** Carfilzomib (PubChem CID 11556711)
- **Diseases:** multiple myeloma (MONDO:0009693), heart failure (MONDO:0005252), arrhythmia (MONDO:0007263), ischemic heart disease (MONDO:0024644)

## Full-text entities

- **Diseases:** hypertension (MESH:D006973), cardiovascular disease (MESH:D002318), multiple myeloma (MESH:D009101), IHD (MESH:D017202), hematological malignancies (MESH:D019337), cancer (MESH:D009369), arrhythmia (MESH:D001145), heart failure (MESH:D006333), cardiac toxicities (MESH:D066126)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11983411/full.md

## References

90 references — full list in the complete paper: https://tomesphere.com/paper/PMC11983411/full.md

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Source: https://tomesphere.com/paper/PMC11983411