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. 2018 Apr;10(Suppl 7):S838-S845.
doi: 10.21037/jtd.2018.04.08.

The role of liquid biopsy in predicting post-operative recurrence of non-small cell lung cancer

Affiliations

The role of liquid biopsy in predicting post-operative recurrence of non-small cell lung cancer

Hengrui Liang et al. J Thorac Dis. 2018 Apr.

Abstract

Background: Radical resection is the cornerstone for patients with early stage of non-small cell lung cancer (NSCLC). However, fatal disease recurs in about 30-70% of resected cases. The circulating tumor cells (CTCs) is one of the main causes of recurrence of cancer. Circulating tumor DNA (ctDNA) is also a potential predictive biomarker of recurrence in patients with early stage NSCLC. A meta-analysis was conducted to identify the prognostic value of the CTCs and ctDNA in predicting the disease recurrence after surgery of NSCLC patients.

Methods: Electronic databases were comprehensively searched for eligible studies. A random effects model was used. The primary endpoint was the hazards ratio (HR) for the disease-free survival (DFS) between CTCs/ctDNA positive and negative groups. The relative risks (RR) of one and two-year recurrence rate between CTCs/ctDNA positive and negative groups were also calculated.

Results: A total of 5 studies involving 351 patients were included, in which 3 were studies on CTCs and 2 were ctDNA. Our result revealed that positive peripheral blood CTCs (HR, 3.37; 95% CI: 2.28-4.96; P<0.001) and ctDNA (HR, 8.15; 95% CI: 2.11-31.50; P=0.002) indicated poor prognosis for DFS. One (68% vs. 18.2%; RR 3.28; P<0.001) and two (76% vs. 44%; RR 1.80; P=0.06) years recurrence rate were higher in CTCs positive group compared with the negative group, respectively. The same result was also observed in ctDNA positive versus negative groups of 1 (77.9% vs. 8.3%; RR 9.05; P=0.001) and 2 (85.6% vs. 8.3%; RR 9.63; P<0.001) years recurrence rate.

Conclusions: Both postoperative CTCs and ctDNA are promising predictive biomarkers of early tumor recurrence in NSCLC patients. In addition, detection based on ctDNA seems to be more sensitive than CTCs.

Keywords: Non-small cell lung cancer (NSCLC); circulating tumor DNA (ctDNA); circulating tumor cell (CTC); recurrence.

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Conflict of interest statement

Conflicts of Interest: The authors have no conflicts of interest to declare.

Figures

Figure 1
Figure 1
Flow diagram detailing the search strategy and identification of studies.
Figure 2
Figure 2
The correlation of CTCs/ctDNA with tumor recurrence in post-operative NSCLC patients. CTCs, circulating tumor cells; ctDNA, circulating tumor DNA; NSCLC, non-small cell lung cancer.
Figure 3
Figure 3
The correlation of CTCs/ctDNA with one-year recurrence rate. CTCs, circulating tumor cells; ctDNA, circulating tumor DNA.
Figure 4
Figure 4
The correlation of CTCs/ctDNA with two-year recurrence rate. CTCs, circulating tumor cells; ctDNA, circulating tumor DNA.

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