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Cardiovascular Complications of Novel Anti-Cancer Immunotherapy: Old Problems from New Agents?
Woo Baek Chung1, Jong Chan Youn1, Ho Joong Youn2
1Division of Cardiology, Department of Internal Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Abstract:
Many novel anti-cancer therapies have dramatically improved outcomes of various cancer patients. However, it also poses a risk for cardiovascular complications as well. For the novel anti-cancer agent with which physicians does not have enough clinical experiences to determine the characteristics of cardiovascular complications, it is important to assess risk factors for cardiotoxicity before starting anti-cancer therapy. High-risk patient should be consulted to cardiologist before initiating anti-cancer therapy and pre-emptive cardiac function monitoring plan might be prepared in advance. The biomarkers, electrocardiography and echocardiography are useful tools for the detection of subclinical cardiotoxicity during anti-cancer therapy. This review article tried to suggest the cardiac function monitoring strategies for newly encountered potential cardiotoxic anti-cancer agents and to summarize the cardiovascular complications of novel anti-cancer immunotherapies including immune checkpoint inhibitor (ICI) and chimeric antigen receptor (CAR) T-cell therapy. ICIs can cause fatal myocarditis, which usually occurs early after initiation, and prompt treatment with high-dose corticosteroid is necessary. CAR T-cell therapy can cause cytokine release syndrome, which may result in circulatory collapse. Supportive treatment as well as tocilizumab, an anti-interleukin-6 receptor antibody are cornerstones of treatment.
Insights
Novel cancer therapies can cause heart problems. Early risk assessment and monitoring are crucial for patients receiving new anti-cancer treatments, especially immune checkpoint inhibitors (ICIs) and CAR T-cell therapy, to prevent cardiotoxicity.
Area of Science:
- Cardio-oncology
- Translational medicine
- Immunotherapy
Background:
- Novel anti-cancer therapies offer improved patient outcomes but carry risks of cardiovascular complications.
- Limited clinical experience with new anti-cancer agents necessitates proactive assessment of cardiotoxicity risk factors.
- Cardiovascular complications can arise from advanced cancer treatments, impacting patient safety and treatment efficacy.
Purpose of the Study:
- To propose cardiac function monitoring strategies for novel, potentially cardiotoxic anti-cancer agents.
- To review cardiovascular complications associated with novel anti-cancer immunotherapies, including immune checkpoint inhibitors (ICIs) and chimeric antigen receptor (CAR) T-cell therapy.
- To emphasize the importance of pre-treatment risk assessment and cardiologist consultation for high-risk patients.
Main Methods:
- Review of current literature on cardiotoxicity associated with novel anti-cancer therapies.
- Analysis of cardiovascular complications from immune checkpoint inhibitors (ICIs) and CAR T-cell therapy.
- Discussion of diagnostic tools such as biomarkers, electrocardiography, and echocardiography for detecting subclinical cardiotoxicity.
Main Results:
- Immune checkpoint inhibitors (ICIs) can induce potentially fatal myocarditis, requiring early, high-dose corticosteroid treatment.
- CAR T-cell therapy is associated with cytokine release syndrome, which can lead to circulatory collapse, managed with supportive care and tocilizumab.
- Biomarkers, ECG, and echocardiography are vital for monitoring cardiac function and detecting subclinical cardiotoxicity during treatment.
Conclusions:
- Proactive cardiac risk assessment and tailored monitoring plans are essential for patients undergoing novel anti-cancer therapies.
- Early detection and prompt intervention are critical for managing cardiotoxicity, particularly myocarditis from ICIs and cytokine release syndrome from CAR T-cell therapy.
- Collaboration between oncologists and cardiologists is vital to optimize patient care and mitigate cardiovascular risks associated with modern cancer treatments.
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