Circulating free plasma tumor DNA in patients with advanced gastric cancer receiving systemic chemotherapy

被引:28
作者
Costa Normando, Savia Raquel [1 ]
Delgado, Pamela de Oliveira [1 ]
Soares Barbosa Rodrigues, Ana Katherine [2 ]
David Filho, Waldec Jorge [1 ]
Affonso Fonseca, Fernando Luiz [1 ]
Silva Melo Cruz, Felipe Jose [1 ,2 ]
del Giglio, Auro [1 ,2 ]
机构
[1] ABC Fdn, Sch Med, Discipline Hematol & Oncol, Santo Andre, Brazil
[2] IBCC, Sao Paulo, Brazil
关键词
Gastric cancer; Circulating free plasma tumorDNA; Total cell-free circulating DNA; Liquid biopsy;
D O I
10.1186/s12907-018-0079-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundAdvanced gastric cancers are usually associated with incurable conditions for which systemic treatments are indicated. Recent studies suggest that circulating cell-free plasma DNA of tumour origin (tDNA) is a promising non-invasive biomarker that can be used to predict the prognosis and monitor the efficacy of systemic treatments in patients with certain types of cancer. We conducted a pilot study to analyse the potential role of tDNA as a biomarker in patients with advanced gastric cancer.MethodsWe included 30 patients with locally advanced unresectable or metastatic gastric cancer. We obtained samples (10mL of total blood) from each patient every 3 months and performed concomitant CT until disease progression or death. Total cell-free circulating DNA (cfDNA) samples were measured using GeneQuant RNA/DNA Calculator-Amersham Pharmacia Biotech (Biochrom) Ltd. The cfDNA was used to evaluate the ALU DNA sequences 247 and 115. The level of tDNA was calculated from the ratio of the expression of ALU DNA sequences and the concentration of total cell-free DNA. We utilized the RECIST criteria 1.1 to evaluate the tumour response.ResultsPatients with advanced gastric cancer had significantly higher concentrations of cfDNA compared with normal controls (p=0.00015), which allowed us to conclude that the cfDNA in the patients originated from the tumour. We did not find any significant correlation between the level of tDNA and OS or tumour response. However, after the first cycles of chemotherapy (at 3 months), we observed that patients with lower tDNA levels had significantly longer DFS compared with those with higher levels (Cox Regression p=0.0228).ConclusionsAt 3 months after the beginning of chemotherapy, the tDNA levels are correlated with DFS in patients with advanced gastric cancer who receive systemic chemotherapy. tDNA may be a specific, non-invasive and cost effective new biomarker for these patients.
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