Anthracycline-induced cardiorenal toxicity: from molecular mechanisms to clinical management - Scorecard - MDSpire

Anthracycline-induced cardiorenal toxicity: from molecular mechanisms to clinical management

  • By

  • Linke Jiao

  • Chao Yuan

  • Li Wang

  • Yating Zhao

  • Guoxia Zhang

  • Xinyu Yang

  • Yonghong Gao

  • Fan Yang

  • Xinye Li

  • Na An

  • Hongcai Shang

  • Yanwei Xing

  • May 12, 2026

  • 0 min

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Clinical Scorecard: Cardiorenal Toxicity Induced by Anthracyclines: Insights into Molecular Mechanisms and Clinical Strategies for Management

At a Glance

CategoryDetail
ConditionAnthracycline-induced cardiorenal toxicity
Key MechanismsDirect nephrotoxicity, cardiac dysfunction exacerbating renal injury, oxidative stress, mitochondrial dysfunction, inflammatory responses.
Target PopulationPatients receiving anthracycline therapy, particularly those with pre-existing cardiac or renal dysfunction.
Care SettingOncology clinics.

Key Highlights

  • Anthracyclines are associated with significant cardiotoxicity and nephrotoxicity.
  • The incidence of cardiotoxicity ranges from 5% to 48%, with dose-dependent patterns.
  • Renal injury occurs in approximately 12%–18% of patients receiving doxorubicin.
  • Cardiorenal interactions can exacerbate overall disease burden.
  • Dexrazoxane is the only approved cardioprotective agent, with limited renoprotective effects.

Guideline-Based Recommendations

Diagnosis

  • Monitor cardiac biomarkers and renal function tests in patients receiving anthracyclines.

Management

  • Consider the use of dexrazoxane for cardioprotection in high-risk patients.

Monitoring & Follow-up

  • Regular assessment of cardiac and renal function is essential during anthracycline therapy.

Risks

  • Increased risk of multi-organ damage in elderly patients and those with comorbidities.

Patient & Prescribing Data

Patients undergoing treatment with anthracyclines for malignancies such as breast cancer, lymphoma, and leukemia.

Individual susceptibility varies; some patients tolerate standard doses while others may develop toxicity early.

Clinical Best Practices

  • Implement monitoring strategies for early detection of cardiorenal toxicity.
  • Educate patients about the risks associated with anthracycline therapy.
  • Develop individualized treatment plans considering patient-specific risk factors.

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