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Clinical Trial Summary

This is a single-arm, multicentre study that aims to assess whether Radiomics combining multiparametric MRI and clinical data could be a good predictor of the responses to neoadjuvant chemotherapy in Breast Cancer.


Clinical Trial Description

Patients undergo multiparametric MRI (including T2WI, DWI and DCE-MRI) at baseline, after 2 courses of neoadjuvant chemotherapy, and prior to the surgery at least 8 weeks after the treatment procedure. Patients undergo biopsy test in one week after the baseline MRI scan to detect the biomarkers including ER, PR, Her-2 and Ki-67, which can be used to select the treatment plan referring to the NCCN clinical guidelines. After the surgery, responses to neoadjuvant chemotherapy are determined according to the histopathologically examination of the surgically resected specimens.

After completion of treatment procedure, patients are followed up for 5 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03592004
Study type Observational
Source Chinese Academy of Sciences
Contact Zhenyu Liu, Doctor
Phone 8613466358609
Email zhenyu.liu@ia.ac.cn
Status Recruiting
Phase
Start date July 18, 2018
Completion date June 1, 2022

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