Construction of Molecular Diagnostic Marker Model for Pancreatic Cystic Tumors Based on Pancreatic Cystic Fluid Samples

Sponsor
Zhaoshen Li (Other)
Overall Status
Recruiting
CT.gov ID
NCT05737953
Collaborator
(none)
100
1
23.6
4.2

Study Details

Study Description

Brief Summary

The goal of this observational study is to test in patients with cystic tumor of pancreas.

The main questions it aims to answer are:

Screening of molecular diagnostic markers for pancreatic cystic tumors by cfDNA methylation sequencing of pancreatic cystic fluid and proteomic assays to distinguish benign from malignant and mucinous/non-mucinous, correlate with pathological features, and find molecular features associated with the degree of malignancy.

Participants will Provide post-operative cyst fluid specimens.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: cfDNA methylation sequencing and proteome analysis

Detailed Description

Patients with pancreatic cystic tumors were divided into control, mucinous tumor and non-mucinous tumor groups, and cfDNA molecules and protein molecules that were significantly altered between different groups were found by cfDNA methylation sequencing of pancreatic cystic fluid and proteomic detection techniques. Multi-omics analysis was performed to construct a more efficient molecular diagnostic marker model. Correlating models with pathological features to find molecular features associated with the degree of malignancy.

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Construction of Molecular Diagnostic Marker Models for Pancreatic Cystic Tumors Based on cfDNA Methylation Sequencing and Proteomic Analysis of Pancreatic Cystic Fluid Samples
Actual Study Start Date :
Jul 13, 2022
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Jun 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Mucinous tumour group

Diagnostic Test: cfDNA methylation sequencing and proteome analysis
Sequencing of cfDNA methylation and proteomic analysis of two sets of capsular fluid samples

Non-mucinous tumour group

Diagnostic Test: cfDNA methylation sequencing and proteome analysis
Sequencing of cfDNA methylation and proteomic analysis of two sets of capsular fluid samples

Outcome Measures

Primary Outcome Measures

  1. Types and concentrations of cfDNA and proteins contained in the vesicular fluid [2023-11-31]

    Identification of protein and circulating gene methylation species in cyst fluid and quantification of their concentrations using mass spectrometry. Characterize cfDNA methylation and proteomics of cyst fluid in patients with pancreatic cystic neoplasm (PCN).

Secondary Outcome Measures

  1. Establishment of a diagnostic model for cystic tumors of the pancreas [2023-11-31]

    A machine learning approach was used to further screen for characteristically methylated cfDNA and proteins in PCN patients.Establishment of a diagnostic model for pancreatic cystic tumors.

  2. Establishing a model for the identification of mucus and non-mucus [2023-11-31]

    A machine learning approach was used to further screen for characteristically methylated cfDNA and proteins in PCN patients.To establish a model for the identification of mucinous and non-mucinous.

  3. Development of a progressive benign malignancy prediction model [2023-11-31]

    A machine learning approach was used to further screen for characteristically methylated cfDNA and proteins in PCN patients.Development of a progression benign malignancy prediction model.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Subjects are ≥ 18 years old, regardless of gender;

  • Preoperative imaging examination (EUS, CT, MRI) diagnosed cystic mass of pancreas and suspected cystic tumor;

  • Subjects voluntarily accepted radical resection of pancreatic cystic tumors;

  • Subjects or family members voluntarily sign the informed consent form for clinical research.

Exclusion Criteria:
  • The excised sample does not contain cystic components, or the cystic fluid cannot be collected;

  • Receive tumor-related treatment (radiotherapy, chemotherapy, immunotherapy, etc.) before operation;

  • Receive antibiotic treatment within 1 week before operation;

  • Subjects refused to accept radical resection of pancreatic cystic tumor, or had any situation that they could not accept radical resection of pancreatic cystic tumor;

  • The subjects or their families refused to sign the informed consent form for clinical research.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Changhai Hospital Shanghai Shanghai China 200433

Sponsors and Collaborators

  • Zhaoshen Li

Investigators

  • Principal Investigator: Shiyu Li, Changhai Hospital
  • Study Chair: Chengye Pan, Changhai Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Zhaoshen Li, Director of Gastroenterology Department of Changhai Hospital, Changhai Hospital
ClinicalTrials.gov Identifier:
NCT05737953
Other Study ID Numbers:
  • WKX2023-02
First Posted:
Feb 21, 2023
Last Update Posted:
Feb 21, 2023
Last Verified:
Feb 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Zhaoshen Li, Director of Gastroenterology Department of Changhai Hospital, Changhai Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 21, 2023