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Clinical Trials in China / NCT06649565
Recruiting Observational

Prospective Validation and Application of an Artificial Intelligence-based Model for Evaluating the Efficacy of Breast Cancer Patients After Neoadjuvant Therapy

NCT06649565 · tracked via the Priya Life Science China tracker
Sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Phase
Observational
Started
2024-01-01
Last updated
2024-10-18

Condition(s) studied

Breast Cancer

Investigational drug(s) / intervention(s)

no intervention

no intervention: no intervention

Study summary

Breast cancer has become the world's number one cancer. While its therapeutic efficacy is increasing, how to achieve non-invasive evaluation of the efficacy of neoadjuvant therapy (NAT) for breast cancer patients and thus avoid surgery has become a bottleneck problem that needs to be broken through in clinical diagnosis and treatment. Existing non-invasive evaluation strategies are limited to single-center, single-modality modeling, and have problems such as low performance and poor versatility. Therefore, in the early stage of this study, multi-modality breast cancer patient data from multiple centers across the country were collected and the establishment of an artificial intelligence (AI) efficacy prediction model was preliminarily completed. On this basis, this project intends to further improve the multi-center prospective validation study of the prediction model. The research results will help solve the scientific problem of non-invasive judgment of NAT efficacy in breast cancer patients and provide a new paradigm for the research of high-performance AI diagnosis and treatment auxiliary systems applicable to multiple centers.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Patients who were treated in the above research centers between January 1, 2024 and October 31, 2025; * ≥18 years old, female, ECOG score ≤2; * Pathological biopsy confirmed invasive breast cancer; * AJCC (8th edition) stage I-III; * MRI imaging data before and after neoadjuvant therapy; * Planned mastectomy or breast-conserving surgery after neoadjuvant therapy, and postoperative pathological information obtained. Exclusion Criteria: * Bilateral breast cancer, multiple lesions, or occult breast cancer; * Poor MRI data quality; * Patients who had received other anti-tumor treatments before enrollment; * Patients with other malignant tumors

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Sanhuan Cancer Hospital, Chaoyang District, Beijing(Cancer Hospital, Chinese Academy of Medical Sciences, close medical alliance) Beijing Beijing Municipality Recruiting
Cancer Hospital, Chinese Academy of Medical Sciences Beijing Beijing Municipality Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06649565 on ClinicalTrials.gov ↗ ← All trials in China