Head-to-head comparison of the diagnostic value of fecal and serum carcinoembryonic antigen for colorectal cancer detection.
2/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
with and without mechanical homogenization.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
In conclusion, fCEA is inferior to sCEA as a non-invasive biomarker for CRC detection.
OpenAlex 토픽 ·
Colorectal Cancer Screening and Detection
Radiopharmaceutical Chemistry and Applications
Intraperitoneal and Appendiceal Malignancies
This study aimed to conduct a head-to-head comparison of the diagnostic value of serum carcinoembryonic antigen (sCEA) and fecal CEA (fCEA) for colorectal cancer (CRC) detection.
- p-value p < .001
- p-value p = .067
- Sensitivity 85%
- Specificity 36.2%
APA
Xianzhe Li, Zitong Zhao, et al. (2026). Head-to-head comparison of the diagnostic value of fecal and serum carcinoembryonic antigen for colorectal cancer detection.. International journal of cancer. https://doi.org/10.1002/ijc.70435
MLA
Xianzhe Li, et al.. "Head-to-head comparison of the diagnostic value of fecal and serum carcinoembryonic antigen for colorectal cancer detection.." International journal of cancer, 2026.
PMID
41957956 ↗
Abstract 한글 요약
This study aimed to conduct a head-to-head comparison of the diagnostic value of serum carcinoembryonic antigen (sCEA) and fecal CEA (fCEA) for colorectal cancer (CRC) detection. Fecal and serum samples from 80 CRC cases at various tumor stages and 100 controls free of colorectal neoplasms at screening colonoscopy were randomly selected from two ongoing large prospective CRC detection studies (IDA and BLITZ) for CEA measurements. Fecal samples were processed using two methods: with and without mechanical homogenization. Diagnostic performance (area under the curve value [AUC], sensitivity) of fCEA and sCEA was compared individually and in combination with fecal immunochemical test (FIT). The fCEA concentrations obtained using both sample processing methods were highly correlated in both CRC cases and controls, but neither correlated with sCEA. The sCEA concentrations demonstrated significantly greater differences between the CRC and control group compared to fCEA concentrations. The diagnostic performance of fCEA obtained with both fecal sample processing methods was significantly lower than that of sCEA (AUC: 0.62 and 0.57 vs. 0.83, both p < .001; sensitivity at 85% specificity: 36.2% and 26.2% vs. 52.5%, p = .067 and .002). Algorithms combining sCEA with fCEA did not significantly improve the diagnostic performance compared to sCEA alone. Combining FIT with sCEA improved diagnostic performance over FIT alone. However, combining FIT with fCEA showed no improvement. In conclusion, fCEA is inferior to sCEA as a non-invasive biomarker for CRC detection. Combination of FIT with sCEA demonstrates greater potential for CRC screening than combination of FIT with fCEA.
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