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Cancer Therapy Guided by Mutation Tests: Current Status and Perspectives
Svetlana N Aleksakhina1,2, Evgeny N Imyanitov1,2
1Department of Tumor Growth Biology, N.N. Petrov Institute of Oncology, 197758 Saint-Petersburg, Russia.
International Journal of Molecular Sciences
|October 23, 2021
Summary
Genomic testing guides cancer drug selection, improving patient outcomes. Tailored treatments based on specific genetic alterations in tumors are becoming standard care for many cancers.
Area of Science:
- Oncology
- Genomics
- Pharmacology
Background:
- Cancer drug efficacy is often linked to a patient's genetic makeup.
- Specific genetic alterations (e.g., EGFR, BRAF, HER2) influence treatment strategies.
- Tumor genomic profiling provides actionable insights for personalized medicine.
Purpose of the Study:
- To review the role of genetic testing in tailoring cancer drug administration.
- To highlight the impact of genomic alterations on treatment selection across various cancer types.
- To emphasize the growing importance of agnostic genomic testing in oncology.
Main Methods:
- Review of current literature on cancer genomics and targeted therapies.
- Analysis of genetic testing requirements for common cancers like lung, colorectal, and breast cancer.
- Discussion of multilocus assays and agnostic testing approaches.
Main Results:
- Genetic alterations such as EGFR, BRAF, HER2, ALK, MET, and KRAS mutations/amplifications necessitate specific drug choices.
- Tumor mutation burden and DNA repair deficiencies are key genomic characteristics.
- Genomically tailored treatments have significantly improved outcomes for many cancer patients.
Conclusions:
- Personalized cancer therapy guided by genetic testing is revolutionizing patient care.
- Comprehensive genomic profiling across all tumor types is increasingly adopted.
- Targeted treatments based on specific genomic events offer substantial benefits in cancer treatment.
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