Application of Chromosomal Instability in Early Diagnosis of Biliary Tract Carcinoma
Study Details
Study Description
Brief Summary
Chromosomal instability (CIN) refers to ongoing chromosome segregation errors throughout consecutive cell divisions. CIN is a hallmark of human cancer, and it is associated with poor prognosis, metastasis, and therapeutic resistance. Analyzing CIN of the DNA extracted from cast-off cells in bile samples seems a promising method for diagnosing, monitoring, and predicting the prognosis of biliary tract carcinoma patients. CIN can be assessed using experimental techniques such as bulk DNA sequencing, fluorescence in situ hybridization (FISH), or conventional karyotyping. However, these techniques are either time-consuming or non-specific. The investigators here intend to study whether a new method named Bile Ultrasensitive Chromosomal Aneuploidy Detection (BileCAD), which is based on low-coverage whole-genome sequencing, can be used to analyze CIN and microbial infection analysis thus help diagnosing and treating biliary tract carcinoma patients.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed Description
Biliary tract carcinoma account for about 3% of all digestive system tumors, with potential high metastasis and invasion ability. Their early clinical symptoms lack specificity, and they are often found in late stage with poor prognosis. CIN results from errors in chromosome segregation during mitosis, leading to structural and numerical chromosomal abnormalities. It will generate genomic heterogeneity that acts as a substrate for natural selection. Furthermore, it is proved that tumors with aneuploidies and polyploidy resulting from whole-genome doubling are related with metastasis, treatment resistance, and decreased overall survival. It is estimated that 60%-80% of human tumors exhibit chromosomal abnormalities suggestive of CIN. CIN positively correlates with tumor stage and is enriched in relapsed as well as metastatic tumor specimens. Due to the ubiquity of CIN in cancer cells, it is a potentially way to detect CIN in the cast-off cells from the bile samples for diagnosing and monitoring biliary tract carcinoma patients. BileCAD is a new method to detecting CIN in the DNA sample from patients, including extracting DNA from bile, analyzing DNA by low-coverage whole-genome sequencing, processing the data by bio-information techniques, and finally optimizing the management of biliary tract carcinoma patients.The investigators intended to conduct a prospective study by analyzing bile samples from gallbladder cancers and cholangiocarcinoma patients and control groups that without any tumor in the Bile duct and gallbladder or other organs to compare the specificity and sensitivity of BileCAD test for diagnosing biliary tract carcinoma to other modalities, such as pathological diagnosis. At the same time, the consistency of BileCAD microbial analysis results and clinical microbial culture results was compared, so as to provide more reference for clinical diagnosis.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Biliary tract carcinoma patients Biliary tract carcinoma patients will be the experimental group to determine the sensitivity of BileCAD analysis. |
Diagnostic Test: The extracted DNA from bile samples will be analyzed by BileCAD to determine the level of CIN.
The extracted gDNA from bile sample will be analyzed by BileCAD to determine the level of CINs.
|
| Non-cancer participants Patients Non-cancer participants Patients being treated for other diseases but without any tumor will provide a negative control to provide data for determining the specificity of BileCAD analysis. |
Diagnostic Test: The extracted DNA from bile samples will be analyzed by BileCAD to determine the level of CIN.
The extracted gDNA from bile sample will be analyzed by BileCAD to determine the level of CINs.
|
Outcome Measures
Primary Outcome Measures
- Sensitivity of bile sample analysis by BileCADanalysis [12 months]
Number of patients "declared positive" with the BileCAD test among the patients suffered from biliary tract carcinoma.
- Specificity of bile sample analysis by BileCADanalysis [12 months]
Number of patients "declared negative" with the BileCAD test among the patients without cancer.
Secondary Outcome Measures
- BileCAD microbial analysis results [12 months]
Consistency of BileCAD microbial analysis results with clinical microbial culture results
- BileCAD analyzed the sensitivity of different types and locations of malignant tumors [12 months]
The tumors were classified into different types and sites and the sensitivity of BileCAD to different types and sites of malignant tumors was calculated.
Eligibility Criteria
Criteria
Inclusion Criteria:
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No systemic therapy or biliary tract surgery before the trial.
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Gallstones, bile duct space, obstructive jaundice and other suspected patients with biliary tract carcinoma.
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Male or female patients aged >= 18 years.
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Participants signed informed consent form.
Exclusion Criteria:
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Age under 18 years.
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Individuals unwilling to sign the consent form or unwilling to provide the medical record.
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Individuals unwilling to participate in this trial.
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Individuals has any active autoimmune disease or history of autoimmune disease.
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Individuals have cardiac clinical symptoms or diseases that are not well controlled.
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Individuals have uncontrolled severe cerebrovascular, pulmonary and other diseases.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Taizhou Hospital of Zhejiang Province | Taizhou | Zhejiang | China |
Sponsors and Collaborators
- Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University
Investigators
- Principal Investigator: fabiao zhang, Taizhou Hospital
Study Documents (Full-Text)
None provided.More Information
Publications
- Al-Rawi DH, Bakhoum SF. Chromosomal instability as a source of genomic plasticity. Curr Opin Genet Dev. 2022 Jun;74:101913. doi: 10.1016/j.gde.2022.101913. Epub 2022 May 5.
- Bach DH, Zhang W, Sood AK. Chromosomal Instability in Tumor Initiation and Development. Cancer Res. 2019 Aug 15;79(16):3995-4002. doi: 10.1158/0008-5472.CAN-18-3235. Epub 2019 Jul 26.
- Liu Y, Yeh MM. Bile duct dysplasia and associated invasive carcinoma: clinicopathological features, diagnosis, and practical challenges. Hum Pathol. 2023 Feb;132:158-168. doi: 10.1016/j.humpath.2022.06.012. Epub 2022 Jun 14.
- Onoyama T, Matsumoto K, Koda H, Yamashita T, Kurumi H, Kawata S, Takeda Y, Harada K, Yashima K, Isomoto H. Diagnostic usefulness of KL-6 concentration of bile in biliary tract cancer. Mol Clin Oncol. 2018 Apr;8(4):561-566. doi: 10.3892/mco.2018.1571. Epub 2018 Feb 12.
- Richardson TE, Walker JM, Abdullah KG, McBrayer SK, Viapiano MS, Mussa ZM, Tsankova NM, Snuderl M, Hatanpaa KJ. Chromosomal instability in adult-type diffuse gliomas. Acta Neuropathol Commun. 2022 Aug 17;10(1):115. doi: 10.1186/s40478-022-01420-w.
- BileCAD-330