Why the study?
Targeted therapies in NSCLC carry drug-specific safety profiles not fully captured in clinical trials, and the real range and frequency of cardiotoxicity remain unknown.
What is the current knowledge regarding cardiotoxicity related to targeted therapies in oncogene-addicted NSCLC?
What is the current knowledge regarding cardiotoxicity related to targeted therapies in oncogene-addicted NSCLC?
This review highlights the emerging issue of cardiotoxicity associated with targeted therapies in NSCLC, emphasizing the need for careful management and prevention strategies in clinical practice.
Raises awareness for cardiotoxicity monitoring in targeted NSCLC therapy; leaves open standardized prevention strategies.
The treatment of Non Small Cell Lung Cancer (NSCLC) has been revolutionised by the introduction of targeted therapies. With the improvement of response and frequently of overall survival, however, a whole new set of adverse events emerged. In fact, due to the peculiar mechanism of action of each one of the tyrosine kinase inhibitors and other targeted therapies, every drug has its own specific safety profile. In addition, this safety profile could not fully emerge from clinical trials data, as patients in clinical practice usually have more comorbidities and frailties. Cardiotoxicity is a well-known and established adverse event of anti-cancer therapies. However, only recently it has become a central topic for targeted therapies in NSCLC, due to the unknown real range and frequency. Management of this toxicity begins with prevention, and must balance the need of continuing an effective anticancer treatment versus low risk of even fatal events and the preservation of long-term quality of life. The aim of this review is to summarise the current knowledge focusing on currently used targeted therapies in NSCLC.
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Torresan et al. (2025) studied this question.
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