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Updated: Feb 11, 2026

Nerve Excitability Assessment in Chemotherapy-induced Neurotoxicity
Published on: April 26, 2012
Pharmacogenetics of Chemotherapy-Induced Cardiotoxicity
Vivian Y Chang1,2, Jessica J Wang3
1Department of Pediatrics, Division of Hematology/Oncology, University of California, Los Angeles, 10833 Le Conte Avenue, Los Angeles, CA, 90095, USA.
Purpose Of Review:
The goal of this review is to summarize current understanding of pharmacogenetics and pharmacogenomics in chemotherapy-induced cardiotoxicity.
Recent Findings:
Most of the studies rely on in vitro cytotoxic assays. There have been several smaller scale candidate gene approaches and a handful of genome-wide studies linking genetic variation to susceptibility to chemotherapy-induced cardiotoxicity. Currently, pharmacogenomic testing of all childhood cancer patients with an indication for doxorubicin or daunorubicin therapy for RARG rs2229774, SLC28A3 rs7853758, and UGT1A6*4 rs17863783 variants is recommended. There is no recommendation regarding testing in adults. There is clear evidence pointing to the role of pharmacogenetics and pharmacogenomics in cardiotoxicity susceptibility to chemotherapeutic agents. Larger scale studies are needed to further identify susceptibility markers and to develop pharmacogenomics-based risk profiling to improve quality of life and life expectancy in cancer survivors.
Insights
Pharmacogenetics and pharmacogenomics help understand chemotherapy-induced cardiotoxicity. Genetic testing is recommended for children receiving specific chemotherapy, but more research is needed for adults.
Area of Science:
- Pharmacology
- Genetics
- Oncology
Background:
- Chemotherapy-induced cardiotoxicity is a significant concern for cancer patients.
- Understanding genetic predispositions can personalize treatment and mitigate risks.
Purpose of the Study:
- To review current knowledge on pharmacogenetics and pharmacogenomics in chemotherapy-induced cardiotoxicity.
- To highlight the role of genetic variations in susceptibility to cardiotoxic effects of chemotherapy.
Main Methods:
- Review of existing literature, including in vitro cytotoxic assays, candidate gene studies, and genome-wide association studies.
- Analysis of current recommendations for pharmacogenomic testing in specific patient populations.
Main Results:
- Genetic variations influence susceptibility to chemotherapy-induced cardiotoxicity.
- Pharmacogenomic testing is recommended for pediatric patients receiving doxorubicin or daunorubicin therapy, targeting specific gene variants (RARG rs2229774, SLC28A3 rs7853758, UGT1A6*4 rs17863783).
- No specific testing recommendations currently exist for adult patients.
Conclusions:
- Pharmacogenetics and pharmacogenomics play a clear role in cardiotoxicity susceptibility.
- Larger studies are essential to identify more susceptibility markers and develop risk profiling for improved outcomes in cancer survivors.
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