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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06278064
Other study ID # BFHHZML20240006
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 1, 2024
Est. completion date June 30, 2025

Study information

Verified date February 2024
Source Beijing Friendship Hospital
Contact Li Min, Ph.D.
Phone +86 13552652141
Email minli@ccmu.edu.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study constitutes a case-control investigation employing a retrospective approach. Plasma samples from individuals with esophageal cancer, benign esophageal diseases, gastric cancer, benign gastric diseases, and a healthy control group were systematically collected. Advanced Data-Independent Acquisition (DIA) proteomics and single-vesicle membrane protein detection techniques were employed to quantify protein content within exosomes. Specific protein biomarkers indicative of early-stage upper gastrointestinal tumors were identified. External validation of these protein markers was conducted using Parallel Reaction Monitoring (PRM) technology on an independent validation cohort. The objective is to establish protein marker predictions for early diagnosis of upper gastrointestinal tumors and prognostication of therapeutic efficacy.


Description:

This study employs a multicenter, retrospective cohort design, collecting and analyzing plasma and tissue exosome protein data from patients with upper gastrointestinal tumors (Stage I-II), upper gastrointestinal benign diseases, and a healthy control group who have visited Beijing Friendship Hospital, and other relevant sub-center hospitals over the past five years. Concurrently, relevant clinical and pathological information is recorded. Samples from the training cohort undergo traditional quantitative exosome proteomic analysis (Data-Independent Acquisition, DIA) and single-vesicle membrane protein analysis (PBA). A comprehensive upper gastrointestinal tumor-specific exosome protein database is constructed, incorporating extensive information. Subsequently, bioinformatics methods are employed to conduct in-depth analysis of the extensive protein data, screening for proteins with high specificity for upper gastrointestinal tumors, capable of direct detection on the exosome membrane surface. By establishing and evaluating diagnostic models, we aim to quantify the diagnostic potential of these markers, providing a scientific basis for future early screening methods for upper gastrointestinal tumors. Finally, external validation of these protein markers in an independent validation cohort ensures their reliability and stability across different patient populations. The academic significance of this research lies in its thorough exploration of exosome proteomics in early cancer diagnosis, offering potential innovative breakthroughs for academic progress and clinical practice in this field.


Recruitment information / eligibility

Status Recruiting
Enrollment 562
Est. completion date June 30, 2025
Est. primary completion date December 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Confirmed diagnosis of upper gastrointestinal cancers or benign upper gastrointestinal diseases through gastroscopy and pathological examination. - Collection of plasma samples prior to surgical treatment. - Availability of complete clinical data. Exclusion Criteria: - Previous reception of anti-tumor treatments (including radiotherapy, chemotherapy, etc.) before blood collection. - Coexistence of other systemic tumors. - Absence of plasma sample collection before surgical treatment. - Incomplete clinical data. - Pregnancy status

Study Design


Intervention

Other:
Gastric Cancer
Patients diagnosed with gastric cancer, including early stage gastric and advanced gastric cancer
Esophagus Cancer
Patients diagnosed with esophagus cancer, including early esophagus gastric and advanced esophagus cancer

Locations

Country Name City State
China Beijing Friendship Hospital, Capital Medical University Beijing
China Cancer Hospital Chinese Academy of Medical Sciences Beijing
China The Fourth Hospital of Hebei Medical University Shijiazhuang Hebei

Sponsors (1)

Lead Sponsor Collaborator
Beijing Friendship Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Plasma proteins in patients with gastric cancer The outcome will be tested by Data-Independent Acquisition (DIA) proteomics technology Before receiving treatment for gastric cancer
Primary Plasma proteins in patients with esophagus cancer The outcome will be tested by Data-Independent Acquisition (DIA) proteomics technology Before receiving treatment for esophagus cancer
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