RecruitingNot ApplicableNCT06429891

Research on Early Diagnosis and Clinical Transformation of Nuclide Probe Based on Bioorthogonal-gastric Cancer Mucin Target Visualization


Sponsor

Hua Zhu

Enrollment

50 participants

Start Date

Aug 20, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The symptoms of early gastric cancer are extremely insidious and most patients are identified as advanced at the time of initial diagnosis. Starting from the clinical needs, this project selects solid tumors and pathogenic glycoprotein synthesis of key glycopeptide antigen determinant mucin (MUC) family of multiple molecules as the research object. Based on the digestive system tumor research cohort established in the early stage, this project intends to verify the tumor microenvironment characteristics of the MUC family and gastric cancer treatment resistance through immunohistochemistry, COSMC gene sequencing and other technologies, and screen key MUC family proteins. Based on the discovery of differential recognition of COSMC deficient cells by antibodies, MUC1-targeted specific monoclonal antibody was developed. Further development of spatial mucinomics based on laser ablation inductively coupled plasma mass spectrometry (LA-IPC-MS) and spatial metabolome based on desorption electrospray mass spectrometry (DESI-MS) to analyze the structure and immunosuppressive mechanism of key gastric cancer glycoprotein MUC. After obtaining key targeted antibodies, with the help of biological orthogonal and click chemistry technology, the original clinical translational research based on mucin targeting was carried out, and a high-affinity nuclide conjugate drug (RDC) with "triple binding" of gastric cancer mucin was constructed and clinical translational research was carried out, which provided new ideas for the accurate diagnosis and treatment of gastric cancer in the early stage.


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This study is developing and testing a new type of nuclear medicine imaging probe designed to detect and visualize a specific protein (a mucin target) that is overexpressed in gastric (stomach) cancer cells. The goal is to improve early diagnosis of gastric cancer using advanced imaging technology. **You may be eligible if...** - You are 18 years or older - You have a solid tumor confirmed by tissue biopsy or pathology testing - You have at least one tumor that can be measured on imaging scans - Your expected survival is at least 12 weeks - You are in generally good health (ECOG 0–1) **You may NOT be eligible if...** - You have significant liver or kidney dysfunction - You are pregnant or planning to become pregnant - You cannot remain still for at least 30 minutes during the scan - You refuse to participate - You have claustrophobia or significant mental health conditions - Your doctor determines you are not suitable for this study for any other reason Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUG18F-FDG

All study participants will undergo one 18F-FDG PET/CT scan.


Locations(1)

Beijing Cancer Hospital

Beijing, Beijing Municipality, China

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NCT06429891


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