Evaluation of combined detection of multigene mutation and SDC2/SFRP2 methylation in stool specimens for colorectal cancer early diagnosis

• DOI: 10.1007/s00384-022-04170-2
• Publication Date: 2022-05-02T09:02:36Z
• Authors: Jie Lin; Lijing Zhang; Mengshi Chen; Juan Chen; Yijuan Wu; Tao Wang; Yan Lu; Zhaofen Ba; Xiaowei Cheng; Rongrong Xu; Tian Tian; Aijuan Sun; Tiantian Zhang; Minghong Chen
• Keywords: Adenoma; Proto-Oncogene Proteins B-raf; 0301 basic medicine; Membrane Proteins; DNA Methylation; Sensitivity and Specificity; 3. Good health; Proto-Oncogene Proteins p21(ras); Feces; 03 medical and health sciences; 0302 clinical medicine; Mutation; Biomarkers, Tumor; Humans; Syndecan-2; Colorectal Neoplasms; Early Detection of Cancer

Molecular diagnostics of colorectal cancer (CRC) can be used as an auxiliary approach for patients recommended for colonoscopy, providing more CRC supplemental diagnosis options. This study investigated whether combined detection of KRAS/BRAF/APC mutation and SDC2/SFRP2 methylation can serve as auxiliary diagnostics in clinical management.KRAS/BRAF/APC mutation and SDC2/SFRP2 methylation in stool samples from healthy donors, patients with CRC, advanced adenoma (AA), non-advanced adenoma (NAA), or other gastroenterological diseases were evaluated using quantitative PCR (qPCR) or methylation-specific quantitative PCR (MSP). Test accuracy was determined by evaluating the tests' sensitivity, specificity, positive/negative predictive value (PPV/NPV), or positive/negative likelihood ratio (PLR/NLR).The combined fecal KRAS/BRAF/APC mutation and SFRP2/SDC2 methylation detection test achieved a sensitivity of 88.57% with a PPV of 93.64% and a PLR of 7.10 for CRC patients. In comparison, the corresponding parameters for multigene mutation were 46.67%, 92.59%, and 36.26 and 83.81%, 93.94%, and 7.47, for DNA methylation, separately. The sensitivity of the combined test, gene mutation test, and DNA methylation test approach was 75%, 28.26%, and 72.83%. Furthermore, the specificity of this approach in the NAA group was 79.49%. Meanwhile, the overall diagnostic specificity for the combined test in NAA, healthy control, and interference groups was 88.42%. In addition, the sensitivity of the combined detection method increased with the disease stage in CRC patients and elevated along with the lesion size (≥ 1 cm) in AA patients.Combined detection of fecal KRAS/BRAF/APC mutation and SFRP2/SDC2 methylation has potential application value for the auxiliary diagnosis of CRC and AA.