Efficient detection and post-surgical monitoring of colon cancer with a multi-marker DNA methylation liquid biopsy.
Shengnan JinDewen ZhuFanggui ShaoShiliang ChenYing GuoKuan LiYourong WangRongxiu DingLingjia GaoWen MaTong LuDandan LiZhengzheng ZhangSuili CaiXue LiangHuayu SongLing JiJinlei LiZhihai ZhengFeizhao JiangXiaoli WuJu LuanHuxiang ZhangZhengquan YangCharles R CantorChang XuChunming DingPublished in: Proceedings of the National Academy of Sciences of the United States of America (2021)
Multiplex assays, involving the simultaneous use of multiple circulating tumor DNA (ctDNA) markers, can improve the performance of liquid biopsies so that they are highly predictive of cancer recurrence. We have developed a single-tube methylation-specific quantitative PCR assay (mqMSP) that uses 10 different methylation markers and is capable of quantitative analysis of plasma samples with as little as 0.05% tumor DNA. In a cohort of 179 plasma samples from colorectal cancer (CRC) patients, adenoma patients, and healthy controls, the sensitivity and specificity of the mqMSP assay were 84.9% and 83.3%, respectively. In a head-to-head comparative study, the mqMSP assay also performed better for detecting early-stage (stage I and II) and premalignant polyps than a published SEPT9 assay. In an independent longitudinal cohort of 182 plasma samples (preoperative, postoperative, and follow-up) from 82 CRC patients, the mqMSP assay detected ctDNA in 73 (89.0%) of the preoperative plasma samples. Postoperative detection of ctDNA (within 2 wk of surgery) identified 11 of the 20 recurrence patients and was associated with poorer recurrence-free survival (hazard ratio, 4.20; P = 0.0005). With subsequent longitudinal monitoring, 14 patients (70%) had detectable ctDNA before recurrence, with a median lead time of 8.0 mo earlier than seen with radiologic imaging. The mqMSP assay is cost-effective and easily implementable for routine clinical monitoring of CRC recurrence, which can lead to better patient management after surgery.
Keyphrases
- end stage renal disease
- circulating tumor
- ejection fraction
- newly diagnosed
- free survival
- dna methylation
- high throughput
- chronic kidney disease
- patients undergoing
- high resolution
- peritoneal dialysis
- squamous cell carcinoma
- lymph node
- young adults
- coronary artery disease
- single molecule
- radiation therapy
- circulating tumor cells
- optical coherence tomography
- locally advanced
- childhood cancer