Evaluation of the diagnostic value of YiDiXie™-SS and YiDiXie™-HS in uroepithelial carcinoma

Abstract

Background: Uroepithelial carcinoma is a serious threat to human health and causes heavy economic burden. Enhanced CT is widely used in screening or preliminary diagnosis of uroepithelial tumors. However, false-positive results of enhanced CT will bring unnecessary mental pain, expensive examination costs, physical injuries, and other adverse consequences; while false-negative results of enhanced CT bring delayed treatment, and patients will thus have to bear the adverse consequences of poor prognosis, high treatment costs, poor quality of life, and short survival period. There is an urgent need to find convenient, cost-effective and non-invasive diagnostic methods to reduce the false-negative and false-positive rates of enhanced CT in uroepithelial tumors. The aim of this study was to evaluate the diagnostic value of YiDiXie™-SS and YiDiXie™-HS in uroepithelial carcinoma. Patients and methods: 319 subjects (malignant group, n=240; benign group, n=79) were finally included in this study. Remaining serum samples from the subjects were collected and tested by applying the YiDiXie™ all-cancer detection kit to evaluate the sensitivity and specificity of YiDiXie™-SS and YiDiXie™-HS. Results: The sensitivity of YiDiXie™-SS in enhanced CT-positive patients was 96.3% (95% CI: 96.3% - 98.3%; 158/164)and its specificity was 64.3% (95% CI: 38.8% - 83.7%; 9/14). This means that the application of YiDiXie™-SS reduces the false-positive rate of urological enhanced CT by 64.3% (95% CI: 38.8% - 83.7%; 9/14) with essentially no increase in malignancy leakage. The sensitivity of YiDiXie™-HS in enhanced CT-negative patients was 85.5% (95% CI: 75.9% - 91.7%; 65/76)and its specificity was 84.6% (95% CI: 73.9% - 91.4%; 55/65). This means that the application of YiDiXie™-HS reduces the false-negative rate of urological enhanced CT by 85.5% (95% CI: 75.9% - 91.7%; 65/76). Conclusion: YiDiXie™-SS substantially reduces the rate of urological enhanced CT false positives with essentially no increase in delayed treatment of malignancies. YiDiXie™-HS substantially reduces the false negative rate of urological enhanced CT. YiDiXie™-SS and YiDiXie™-HS have an important diagnostic value in uroepithelial carcinoma, and are expected to solve the problems of "high false-positive rate of urological enhanced CT" and "high false-negative rate of urological enhanced CT" in uroepithelial carcinoma. Clinical Research Registration Number:ChiCTR2200066840. Keywords: Uroepithelial carcinoma, Enhanced CT, False-positive, False-negative, YiDiXie™-SS, YiDiXie™-HS

Competing Interest Statement

The authors have declared no competing interest.

Clinical Trial

ChiCTR2200066840

Funding Statement

This work was supported by Shenzhen High-level Hospital Construction Fund, Clinical Research Project of Peking University Shenzhen Hospital (LCYJ2020002, LCYJ2020015, LCYJ2020020, LCYJ2017001).

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Ethics committee of Peking University Shenzhen Hospital gave ethical approval for this work.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

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I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

All data produced in the present study are contained in the manuscript.

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