Key result
Pharmacogenomic data predicting breast cancer therapy cardiotoxicity remain scarce, focusing primarily on anthracycline and HER2 genes.
Why the study?
Data on single-nucleotide polymorphisms related to breast cancer treatment-induced cardiotoxicity are emerging but remain scarce, retrospective, and heterogeneous.
Can pharmacogenomics predict cardiotoxicity in patients receiving breast cancer therapies?
Can pharmacogenomics predict cardiotoxicity in patients receiving breast cancer therapies?
Pharmacogenomics holds potential for predicting cardiotoxicity in breast cancer patients, but current evidence remains scarce and heterogeneous.
Answers are grounded in this paper and cite their sources.
Data scarcity precludes clinical use of pharmacogenomics for cardiotoxicity prediction; leaves open need for standardized prospective studies.
Pharmacogenomics is an emerging field in oncology, one that could provide valuable input on identifying patients with inherent risk of toxicity, thus allowing for treatment tailoring and personalization on the basis of the clinical and genetic characteristics of a patient. Cardiotoxicity is a well-known side effect of anthracyclines and anti-HER2 agents, although at a much lower incidence for the latter. Data on single-nucleotide polymorphisms related to cardiotoxicity are emerging but are still scarce, mostly being of retrospective character and heterogeneous. A literature review was performed, aiming to describe current knowledge in pharmacogenomics and prediction of cardiotoxicity related to breast cancer systemic therapies and radiotherapies. Most available data regard genes encoding various enzymes related to anthracycline metabolism and HER2 polymorphisms. The available data are presented, together with the challenges and open questions in the field.
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Altena et al. (2022) conducted a review in Cardiotoxicity in breast cancer therapies. Pharmacogenomics was evaluated. Pharmacogenomic data for predicting cardiotoxicity from breast cancer therapies remain scarce and heterogeneous, primarily focusing on genes related to anthracycline metabolism and HER2 polymorphisms.
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