Abstract
Tumor tissue genotyping is used routinely for lung cancer to identify specific targetable oncogenic alterations, including EGFR mutations and ALK rearrangements. However, tumor tissue from a single biopsy is often insufficient for molecular testing, may offer a limited evaluation because of tumor heterogeneity and can be difficult to obtain. Cell-free circulating tumor DNA has been widely investigated as a potential surrogate for tissue biopsy for noninvasive assessment of tumor-related genomic alterations. New techniques have improved EGFR mutations detection in ctDNA, thus supporting the use of this liquid biopsy for predicting response to EGFR tyrosine kinase inhibitors (TKIs) and monitoring the emergence of resistance. The serial evaluation of ctDNA during treatment is feasible and can be used to track tumor changes in real time and for a wide range of clinically useful applications.
| Original language | English |
|---|---|
| Pages (from-to) | 417-30 |
| Number of pages | 14 |
| Journal | Biomarkers in medicine |
| Volume | 10 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 2016 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Biomarkers, Tumor
- Carcinoma, Non-Small-Cell Lung
- DNA, Neoplasm
- Drug Resistance, Neoplasm
- Humans
- Lung Neoplasms
- Mutation
- Protein Kinase Inhibitors
- Receptor Protein-Tyrosine Kinases
- Receptor, Epidermal Growth Factor
- Journal Article
- Review
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