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Feasibility of cell-free circulating tumor DNA testing for lung cancer

  • Mariacarmela Santarpia
  • , Niki Karachaliou
  • , Maria González-Cao
  • , Giuseppe Altavilla
  • , Elisa Giovannetti
  • , Rafael Rosell
  • Medical Oncology Unit, Department of Human Pathology "G. Barresi", University of Messina, Messina, Italy.
  • Dr Rosell Oncology Institute, Quirón Dexeus University Hospital, Barcelona, Spain.

Research output: Contribution to journalArticleAcademicpeer-review

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 languageEnglish
Pages (from-to)417-30
Number of pages14
JournalBiomarkers in medicine
Volume10
Issue number4
DOIs
Publication statusPublished - 2016

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    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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