Peritoneal cell-free DNA as a sensitive biomarker for detection of peritoneal metastasis in colorectal cancer: a prospective diagnostic study: A prospective diagnostic study

被引:5
|
作者
Yuan, Zixu [1 ]
Chen, Wenle [2 ]
Liu, Duo [1 ]
Qin, Qiyuan [1 ]
Grady, William M. [3 ]
Fichera, Alessandro [4 ]
Wang, Huaiming [1 ]
Hou, Ting [5 ]
Lv, Xinze [5 ]
Li, Chanhe [5 ]
Wang, Hui [1 ]
Cai, Jian [6 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 6, Guangdong Inst Gastroenterol, Dept Colorectal Surg,Dept Gen Surg,Guangdong Prov, 26 Yuancun Erheng Rt, Guangzhou 510655, Peoples R China
[2] Zhongshan Municipal Peoples Hosp, Dept Colorectal Surg, Zhongshan, Peoples R China
[3] Fred Hutchinson Canc Res Ctr, Clin Res Div, Seattle, WA USA
[4] Baylor Univ, Med Ctr, Colon & Rectal Surg, Dallas, TX USA
[5] Burning Rock Biotech, Guangzhou, Peoples R China
[6] Shenzhen Univ, Shenzhen Peoples Hosp 2, Affiliated Hosp 1, Dept Colorectal Surg, 3002 Sungang West Rd, Shenzhen, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Peritoneal metastasis; Colorectal cancer; Cell-free DNA; NGS; Driver mutations; HYPERTHERMIC INTRAPERITONEAL CHEMOTHERAPY; CYTOREDUCTIVE SURGERY; GENOME; CARCINOMATOSIS; DISCOVERY;
D O I
10.1186/s13148-023-01479-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The detection of peritoneal metastasis (PM) is limited by current imaging tools. In this prospective study, we aimed to evaluate the sensitivity and specificity of peritoneal cell-free DNA (cfDNA) for diagnosis of PM.Methods Colorectal cancer (CRC) patients with/without PM were enrolled. The cfDNA experimental personnel and statists were blinded to the diagnosis of PM. Ultradeep sequencing covering large genomic regions (35000X, Next-generation sequencing) of cfDNA in peritoneal lavage fluid (FLD) and matched tumor tissues was performed.Results A total of 64 cases were recruited prospectively and 51 were enrolled into final analysis. In training cohort, 100% (17/17) PM patients obtained positive FLD cfDNA, comparing to 5/23 (21.7%) in patients without PM. Peritoneal cfDNA had a high sensitivity of 100% and specificity of 77.3% for diagnosis of PM (AUC: 0.95). In validation group of 11, 5/6 (83%) patients with PM obtained positive FLD cfDNA, comparing to 0/5 in non-PM (P = 0.031) with a sensitivity of 83.3% and specificity of 100%. Positive FLD cfDNA was associated with poor recurrence-free survival (P = 0.013) and was preceding radiographic evidence of recurrence.Conclusions Peritoneal cfDNA is a promising sensitive biomarker for earlier detection of PM in CRC than current radiological tools. It can potentially guide selection for targeted therapies and serve as a surrogate instead of laparoscopic explore in the future.
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页数:14
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