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Cardiotoxicity of Targeted Therapies in Hematologic Malignancies: From Molecular Mechanisms to Clinical Management
Mengmeng Lin1, Shanshan Shi2, Chong Zhang3
1Department of Clinical Pharmacy, Key Laboratory of Clinical Cancer Pharmacology and Toxicology Research of Zhejiang Province, School of Medicine, Affiliated Hangzhou First People's Hospital, Westlake University, 261 Huansha Road, Hangzhou, Zhejiang, 310006, China.
Opinion Statement:
The therapeutic landscape of hematologic malignancies has been transformed over the past decade by the shift from conventional chemotherapy to targeted therapies, including proteasome, tyrosine kinase, and epigenetic regulators. Although these agents have significantly improved patient survival outcomes, this progress is tempered by the emergence of distinct cardiovascular toxicities that threaten both patient quality of life and long-term prognosis. Current clinical management is limited by the lack of standardized adverse event reporting mechanisms in trials and the operational complexity of existing risk stratification tools. In this context, a streamlined, personalized surveillance strategy is warranted. Comprehensive baseline cardiovascular assessment is paramount, with the frequency and modality of subsequent monitoring tailored specifically to the agent's mechanism of action and the patient's underlying risk profile. Crucially, when cardiotoxicity arises, the utilization of multidisciplinary cardio-oncology teams is indicated to manage the cardiac condition therapeutically, thereby avoiding the premature discontinuation of life-saving oncologic therapy. The ultimate goal remains maximizing the potent antitumor efficacy of these targeted therapies while rigorously protecting cardiovascular function.
Insights
Targeted therapies for blood cancers improve survival but can cause heart problems. Personalized monitoring and cardio-oncology teams are essential for managing these cardiovascular toxicities while continuing cancer treatment.
Area of Science:
- Cardio-oncology
- Hematologic Malignancies
- Cardiovascular Toxicology
Background:
- The treatment of hematologic malignancies has shifted towards targeted therapies, improving survival rates.
- These novel agents, including proteasome inhibitors, tyrosine kinase inhibitors, and epigenetic regulators, are associated with significant cardiovascular toxicities.
- Current management strategies for these toxicities are hindered by inconsistent adverse event reporting and complex risk stratification tools.
Purpose of the Study:
- To advocate for a streamlined, personalized surveillance strategy for cardiovascular toxicities in patients receiving targeted cancer therapies.
- To emphasize the importance of comprehensive baseline cardiovascular assessment and tailored monitoring based on treatment specifics and patient risk.
- To highlight the critical role of multidisciplinary cardio-oncology teams in managing emergent cardiotoxicity and preventing treatment interruptions.
Main Methods:
- Review of current literature and clinical practices in cardio-oncology.
- Analysis of challenges in managing cardiovascular adverse events associated with targeted cancer therapies.
- Proposal of a personalized surveillance and management framework.
Main Results:
- The shift to targeted therapies necessitates a proactive approach to managing cardiovascular complications.
- Personalized monitoring, informed by drug mechanisms and patient risk, is crucial for early detection of cardiotoxicity.
- Multidisciplinary cardio-oncology teams are vital for effective management of cardiac issues, ensuring continuity of cancer care.
Conclusions:
- A personalized, risk-stratified surveillance approach is essential for patients undergoing targeted therapy for hematologic malignancies.
- Early detection and proactive management of cardiovascular toxicities by cardio-oncology teams can optimize oncologic outcomes and patient quality of life.
- Balancing the benefits of potent antitumor therapies with the protection of cardiovascular function is paramount.
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