Application of Circulating Tumor DNA as a Biomarker for Non-Small Cell Lung Cancer

Jialiang Yang, Yan Hui, Yanxiang Zhang, Minghui Zhang, Binbin Ji, Geng Tian, Yangqiang Guo, Min Tang, Lianxing Li, Bella Guo, Tonghui Ma

Research output: Contribution to journalReview articlepeer-review

26 Scopus citations

Abstract

Background: Non-small cell lung cancer (NSCLC) is one of the most prevalent causes of cancer-related death worldwide. Recently, there are many important medical advancements on NSCLC, such as therapies based on tyrosine kinase inhibitors and immune checkpoint inhibitors. Most of these therapies require tumor molecular testing for selecting patients who would benefit most from them. As invasive biopsy is highly risky, NSCLC molecular testing based on liquid biopsy has received more and more attention recently. Objective: We aimed to introduce liquid biopsy and its potential clinical applications in NSCLC patients, including cancer diagnosis, treatment plan prioritization, minimal residual disease detection, and dynamic monitoring on the response to cancer treatment. Method: We reviewed recent studies on circulating tumor DNA (ctDNA) testing, which is a minimally invasive approach to identify the presence of tumor-related mutations. In addition, we evaluated potential clinical applications of ctDNA as blood biomarkers for advanced NSCLC patients. Results: Most studies have indicated that ctDNA testing is critical in diagnosing NSCLC, predicting clinical outcomes, monitoring response to targeted therapies and immunotherapies, and detecting cancer recurrence. Moreover, the changes of ctDNA levels are associated with tumor mutation burden and cancer progression. Conclusion: The ctDNA testing is promising in guiding the therapies on NSCLC patients.

Original languageEnglish
Article number725938
JournalFrontiers in Oncology
Volume11
DOIs
StatePublished - 5 Aug 2021
Externally publishedYes

Keywords

  • circulating tumor DNA
  • immunotherapies
  • liquid biopsy
  • molecular testing
  • non-small cell lung cancer
  • therapeutic response

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