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Detection of Rare Mutations in CtDNA Using Next Generation Sequencing
Published on: August 24, 2017
Promising clinical application of ctDNA in evaluating immunotherapy efficacy
Li Li1, Jun Zhang2, Xiaoyue Jiang1
1Department of Oncology, Beijing Friendship Hospital, Capital Medical University Beijing 100050, China.
Abstract:
An increasing number of promising immunotherapies and related clinical trials have led to several major breakthroughs in multiple cancers, but a reliable and precise biomarker for evaluating efficacy and prognosis has not yet been established. As a typical representation of a liquid biopsy, circulating cell-free DNA (ctDNA) possesses the functions and advantages of tissue biopsy but its distinct advantages of convenience, real-time nature, non-invasiveness and homogeneity make it superior to tissue biopsy. Indeed, compared with routine imaging and tumor markers, ctDNA offers an earlier indication and provides more precise information. ctDNA is reportedly able to identify immunotherapy responders, evaluate efficacy and survival time, screen immune checkpoint inhibitor resistance and pseudo-progress and predict tumor recurrence and metastasis. Thus, ctDNA can act as an "Eagle Eye" by comprehensively monitoring both macro- and micro-changes in the immunotherapy process. Although ctDNA has become a research topic of interest, its limitations cannot be ignored, and improvements in its sensitivity and standardization are urgently needed. This review reveals the advantages and limitations of ctDNA as a precise biomarker and supports the feasibility of using ctDNA detection for common monitoring during immunotherapy.
Insights
Circulating cell-free DNA (ctDNA) shows promise as a non-invasive biomarker for monitoring cancer immunotherapy. While effective, improvements in ctDNA sensitivity and standardization are needed for widespread clinical use.
Area of Science:
- Oncology
- Molecular Biology
- Biomarker Discovery
Background:
- Immunotherapies have advanced cancer treatment, yet reliable biomarkers for efficacy and prognosis are lacking.
- Circulating cell-free DNA (ctDNA), a component of liquid biopsies, offers non-invasive monitoring advantages over traditional tissue biopsies.
- Existing methods like imaging and tumor markers have limitations in early detection and precision compared to ctDNA.
Purpose of the Study:
- To review the advantages and limitations of ctDNA as a biomarker in cancer immunotherapy.
- To assess the feasibility of using ctDNA for routine monitoring during immunotherapy.
- To highlight the potential of ctDNA in identifying responders, evaluating efficacy, and predicting outcomes.
Main Methods:
- Literature review of studies on ctDNA in cancer immunotherapy.
- Analysis of ctDNA's role in identifying immunotherapy responders.
- Evaluation of ctDNA's utility in monitoring treatment efficacy, resistance, and patient survival.
Main Results:
- ctDNA can identify immunotherapy responders, evaluate treatment efficacy, and predict survival time.
- It aids in screening for immune checkpoint inhibitor resistance and pseudo-progression.
- ctDNA offers earlier indications and more precise information than routine imaging and tumor markers.
- ctDNA can predict tumor recurrence and metastasis, acting as an "Eagle Eye" for monitoring.
Conclusions:
- ctDNA presents significant advantages as a non-invasive, real-time biomarker for monitoring cancer immunotherapy.
- Further improvements in ctDNA sensitivity and standardization are crucial for its broader clinical application.
- ctDNA holds strong potential for routine monitoring throughout the immunotherapy process.
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