Postoperative Circulating Tumor DNA Can Predict High Risk Patients with Colorectal Cancer Based on Next-Generation Sequencing

被引:6
作者
Lee, Chul Seung [1 ]
Kim, Hoon Seok [2 ,3 ]
Schageman, Jeoffrey [4 ]
Lee, In Kyu [1 ]
Kim, Myungshin [2 ,3 ]
Kim, Yonggoo [2 ,3 ]
机构
[1] Catholic Univ Korea, Coll Med, Dept Surg, Seoul St Marys Hosp, Seoul 06591, South Korea
[2] Catholic Univ Korea, Coll Med, Dept Lab Med, Seoul St Marys Hosp, Seoul 06591, South Korea
[3] Catholic Univ Korea, Coll Med, Catholic Genet Lab Ctr, Seoul St Marys Hosp, Seoul 06591, South Korea
[4] Thermo Fisher Sci, Austin, TX 78701 USA
关键词
circulating tumor DNA; colorectal cancer; next-generation sequencing; CELL-FREE DNA; APC MUTATIONS; COLON-CANCER; ADJUVANT THERAPY; RECURRENCE; RESISTANCE; LANDSCAPE; SURVIVAL; EFFICACY; INVASION;
D O I
10.3390/cancers13164190
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Circulating tumor DNA (ctDNA) is a minimally invasive biomarker useful for monitoring minimum residual disease, recurrence, and treatment response in colorectal cancer (CRC). We analyzed circulating tumor DNA from patients with CRC to evaluate analytical and clinical performances using next-generation sequencing (NGS). It is clear that postoperative circulating tumor DNA detection provides valuable information to determine whether a patient might at high risk of disease recurrence or have a persistent tumor lesion. The NGS assay not only showed excellent analytical performance, but also shows a state-of-art diagnostic option in patient-oriented precision medicine. The objective of this study was to characterize circulating tumor DNA (ctDNA) mutations in colorectal cancer (CRC) patients and evaluate their prognostic values during treatment. Forty-nine patients with CRC planned for operation were enrolled. A total of 115 plasma samples were collected pre-operation, post-operation, and post-chemotherapy. ctDNA analysis was performed using next-generation sequencing (NGS) including 14 genes. In 22 (44.9%) out of 49 patients, at least one mutation (40 total mutations) was detected in the initial plasma sample. The median sum of variant allele frequency was 0.74% (range: 0.10-29.57%). TP53 mutations were the most frequent (17 of 49 patients, 34.7%), followed by APC (18.4%), KRAS (12.2%), FBXW7 (8.2%), NRAS (2.0%), PIK3CA (2.0%), and SMAD4 (2.0%). After surgery, five (14.3%) out of 35 patients harbored ctDNA mutation. All five patients experienced relapse or metastasis during follow-up. It was noteworthy that all three patients with persistent ctDNA relapsed after R0 resection. After chemotherapy, ctDNA analysis was performed for 31 patients, all of which were ctDNA-negative. Analytical and clinical performances of NGS to utilize ctDNA in CRC were determined. Results revealed that postoperative ctDNA might serve as a marker for identifying risk of recurrence, thus contributing to patient-oriented treatment strategies.
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页数:11
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