Prediction of Neoadjuvant Therapy Efficacy and Prognosis for Breast Cancer Based on Multimodal Data

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-80
SponsorYunnan Cancer Hospital

About this trial

This study aims to develop a multimodal deep learning model integrating MRI, ultrasound, digital pathology and clinical information based on multicenter retrospective data. To externally validate the model in an independent prospective cohort, and evaluate its accuracy in predicting pathological complete response (pCR), 3-year and 5-year disease-free survival (DFS). To establish visual tools such as nomograms, assisting clinicians in identifying patients with chemoresistance and facilitating individualized de-escalation or escalation treatment strategies.

Eligibility criteria

Qualifiers

Histopathologically confirmed invasive breast cancer;

Planned to receive a full course of neoadjuvant therapy;

Complete baseline imaging data (MRI/ultrasound/mammography) and core needle pathology results available.

Disqualifiers

Previous history of ipsilateral breast cancer or chest radiotherapy;

Distant metastasis (Stage IV);

Poor image quality or missing clinical data exceeding 20%.

Trial design

Treatments tested in this trial

  • To explore the value of a multimodal deep learning model integrating MRI, ultrasound, digital pathology and clinical information in predicting pCR and long-term prognosis.

Treatment groups

1,800 Participants
are divided into 1 treatment group

Locations

This trial has no locations

Sponsors and collaborators