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A Multicenter Prospective Observational Cohort Study: Predicting Neoadjuvant Chemotherapy Response Using Pre-Treatment DCE-MRI-Based AI Models in HR+/HER2- Breast Cancer

Status: Recruiting
Location: See all (5) locations...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

This study is a multicenter, prospective, observational cohort study to evaluate the predictive performance of pre-treatment DCE-MRI-based artificial intelligence (AI) models for neoadjuvant chemotherapy benefit in HR+/HER2- breast cancer. The study plans to enroll eligible HR+/HER2- breast cancer patients receiving routine standard neoadjuvant chemotherapy and stratify participants into high-benefit and low-benefit subgroups via the established AI model based on baseline breast DCE-MRI images. All enrolled patients will undergo systematic collection of baseline clinical-pathological data, pre-treatment DCE-MRI scans, neoadjuvant chemotherapy regimens, postoperative residual cancer burden (RCB) classification, objective response rate (ORR), and long-term survival endpoints including disease-free survival (DFS) and overall survival (OS). The primary objective compares the rate of RCB 0-1 between AI-defined high-benefit patients and published historical control data; secondary analyses compare ORR, RCB 0-1 proportion, DFS and OS between AI-stratified high-benefit and low-benefit subgroups to comprehensively verify the clinical value of this imaging AI model for individualized neoadjuvant chemotherapy selection.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Female patients aged ≥ 18 years old.

• Histopathologically confirmed invasive breast carcinoma.

• Hormone receptor positive (ER and/or PR ≥1%), HER2-negative status (IHC 0-1+, or IHC 2+ with negative FISH result).

• Clinical stage II-III breast cancer per the 8th AJCC staging system, with clinical indication for neoadjuvant chemotherapy or primary surgery.

• Standard pre-treatment breast DCE-MRI performed before neoadjuvant chemotherapy, with image quality eligible for AI model analysis.

• ECOG performance status 0 or 1; adequate function of major vital organs to tolerate planned clinical treatment.

• Voluntary participation with written informed consent obtained.

Locations
Other Locations
China
Fujian Cancer Hospital
RECRUITING
Fuzhou
Fujian Provincial Hospital
RECRUITING
Fuzhou
Ningde First Hospital
RECRUITING
Ningde
The Second Affiliated Hospital of Fujian Medical University
RECRUITING
Quanzhou
Sanming Second Hospital
RECRUITING
Sanming
Contact Information
Primary
Chuangui Song, doctor
songcg1971@outlook.com
13960709993
Time Frame
Start Date: 2026-06-01
Estimated Completion Date: 2027-06-30
Participants
Target number of participants: 100
Treatments
HR+/HER2- Breast Cancer Cohort Receiving Neoadjuvant Chemotherapy
Multicenter prospective observational cohort of patients with HR+/HER2- invasive breast cancer who receive routine standard neoadjuvant chemotherapy. All participants undergo pre-treatment DCE-MRI scanning, and an MRI-based AI model is applied to stratify patients into high and low chemotherapy benefit subgroups.
Related Therapeutic Areas
Sponsors
Leads: Fujian Cancer Hospital

This content was sourced from clinicaltrials.gov