Predicting Tumor Metastasis by Employing a Target Organ/Primary Lesion Fusion Radiomics Model: a Prospective Observational Trial

Status: Recruiting
Location: See all (2) locations...
Study Type: Observational
SUMMARY

A pre-metastatic target organ/primary lesion fusion radiomics model was developed based on the soil-seed theory to predict comman tumor metastasis in retrospective settings. To prospectively verify the performance of the target organ/primary lesion fusion radiomics model in predicting tumor metastasis patterns (brain metastasis in lung cancer, liver metastasis in colorectal cancer, lung metastasis in breast cancer), we designed this prospective observational trial.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
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• ECOG performance status score 0-2;

• Histologically or cytologically confirmed stage III-IV NSCLC;

• If the baseline pathology is adenocarcinoma, driver gene testing (at least EGFR/ALK/ROS1/KRAS/MET) should be performed;

• Complete imaging data of baseline stage (contrast-enhanced MR For lung cancer, contrast-enhanced MR/CT for colorectal cancer, and chest CT for breast cancer);

• No target organ metastasis on baseline imaging (no brain/liver/lung metastasis for lung cancer/colorectal cancer/breast cancer, respectively);

• Patients received at least one systemic therapy (chemotherapy, targeted therapy, immunotherapy, etc.) and received regular follow-up;

• Regular follow-up during and after treatment;

• Life expectancy ≥6 months;

Locations
Other Locations
China
Fudan University Shanghai Cancer Center
RECRUITING
Shanghai
Fudan University Shanghai Cancer Center
RECRUITING
Shanghai
Contact Information
Primary
Xiao Chu
chuxiao@sibs.ac.cn
15821383376
Time Frame
Start Date: 2024-01-01
Estimated Completion Date: 2027-12
Participants
Target number of participants: 166
Treatments
High risk group
This is a observational study, patients will be assigned to high-risk or low-risk groups (according to a radiomics model) by the investigators. Both the patients and the treating physicians will be blinded to this procedure. No interventions excluding standard treatment procedure executed by the treating physicians.
Low risk group
This is a observational study, patients will be assigned to high-risk or low-risk groups (according to a radiomics model) by the investigators. Both the patients and the treating physicians will be blinded to this procedure. No interventions excluding standard treatment procedure executed by the treating physicians.
Sponsors
Leads: Fudan University

This content was sourced from clinicaltrials.gov