# Reversible Heart Failure After Anthracycline and Alkylating Agent Chemotherapy

**Authors:** Amresh Gul, Zahid Khan

PMC · DOI: 10.7759/cureus.99997 · Cureus · 2025-12-24

## TL;DR

A patient with breast cancer developed heart failure after chemotherapy but showed significant recovery with proper treatment.

## Contribution

This case highlights reversible heart failure following anthracycline and alkylating agent chemotherapy, emphasizing potential for recovery with medical therapy.

## Key findings

- The patient's left ventricular ejection fraction dropped to 39% after chemotherapy.
- With guideline-directed medical therapy, her ejection fraction improved to 45% at six months and 50-55% at 12 months.
- The case demonstrates that chemotherapy-induced heart failure can be reversible with optimized treatment.

## Abstract

Cardiotoxicity, including chemotherapy-induced heart failure (HF), remains a significant and well-recognised complication in modern oncologic practice. As cancer therapies evolve, treatment-related comorbidities continue to pose persistent challenges to patient outcomes and long-term survivorship. Among these, cytostatic-induced cardiotoxicity is particularly concerning due to its multifactorial and complex pathophysiology, involving oxidative stress, mitochondrial dysfunction, and direct myocardial injury. A comprehensive understanding of these mechanisms is essential for developing targeted preventive strategies and evidence-based therapeutic interventions.

We report a case of a 41-year-old Caucasian female who developed chemotherapy-induced cardiomyopathy, or heart failure with reduced ejection fraction (HFrEF), following treatment for right-sided breast cancer. Baseline echocardiogram showed normal biventricular function; however, her left ventricular ejection fraction (LVEF) declined to 39% following dual anthracycline-based chemotherapy, specifically doxorubicin and cyclophosphamide, for breast cancer. The patient was subsequently managed with guideline-directed medical therapy (GDMT). At six- and 12-month follow-up, her LVEF improved to 45% and 50-55%, respectively, demonstrating favourable cardiac recovery under optimised pharmacologic management.

## Linked entities

- **Chemicals:** doxorubicin (PubChem CID 31703), cyclophosphamide (PubChem CID 2907)
- **Diseases:** heart failure (MONDO:0005252), breast cancer (MONDO:0004989)

## Full-text entities

- **Diseases:** cancer (MESH:D009369), mitochondrial dysfunction (MESH:D028361), breast cancer (MESH:D001943), cardiomyopathy (MESH:D009202), Cardiotoxicity (MESH:D066126), HF (MESH:D006333)
- **Chemicals:** doxorubicin (MESH:D004317), Anthracycline (MESH:D018943), cyclophosphamide (MESH:D003520)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12830059/full.md

## References

14 references — full list in the complete paper: https://tomesphere.com/paper/PMC12830059/full.md

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Source: https://tomesphere.com/paper/PMC12830059