Pharmacogenetics for severe adverse drug reactions induced by molecular-targeted therapy

Chihiro Udagawa1, Hitoshi Zembutsu2

  • 1Department of Genetic Medicine and Services, National Cancer Center Hospital, Tokyo, Japan.

Cancer Science
|August 12, 2020
PubMed

Insights

Predicting severe adverse drug reactions (ADRs) from molecular-targeted cancer therapy is crucial. Pharmacogenetics helps identify genetic variants linked to drug toxicity, improving patient treatment selection.

Area of Science:

  • Oncology
  • Pharmacogenetics
  • Drug Safety

Background:

  • Molecular-targeted drugs offer precise cancer cell attack with fewer adverse drug reactions (ADRs).
  • Despite their precision, these drugs can cause severe, potentially life-threatening ADRs.
  • Predicting patient risk for ADRs is increasingly important for safe molecular-targeted therapy.

Purpose of the Study:

  • To review current research on genetic variants and severe ADRs in molecular-targeted cancer therapy.
  • To highlight the role of pharmacogenetics in understanding drug toxicity.
  • To inform personalized therapeutic strategies based on genetic profiles.

Main Methods:

  • Literature review of studies reporting genetic variants and molecular-targeted drug-induced severe ADRs in oncology.
  • Analysis of existing data on genotype-phenotype correlations for drug toxicity.
  • Synthesis of findings to provide an overview of current knowledge.

Main Results:

  • Genetic variants are associated with specific severe ADRs in patients receiving molecular-targeted drugs.
  • Pharmacogenetics offers insights into individual susceptibility to drug toxicity.
  • The relationship between genetic profiles and ADR risk is complex and under active investigation.

Conclusions:

  • Identifying genetic variants can aid in predicting patients at risk for severe ADRs.
  • Pharmacogenetics is a key tool for optimizing molecular-targeted therapy selection.
  • Further research is needed to fully elucidate genotype-specific ADR risks in oncology.

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