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Clinical Trial Summary

This study prospectively included 150 breast cancer patients (30 patients in the first stage and 120 patients in the second stage) who were treated with the commonly used neoadjuvant chemotherapy recommended by NCCN, received surgical treatment after neoadjuvant chemotherapy, and evaluated the efficacy according to the surgical pathological response.Based on the technical analysis of Mammaprint in patients with pathologic complete response (pCR), partial response and no response, we analyzed the characteristic genes related to breast cancer in tumor tissues and evaluated the accuracy and sensitivity of Mammaprint test in the efficacy of neoadjuvant chemotherapy.A new model for predicting NCT effect of breast cancer with combined risk genes and clinical parameters was established based on the clinical characteristic parameters of patients to study the accuracy and sensitivity of Mammaprint monitoring for prognosis determination of breast cancer patients.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Breast Neoplasms
  • Evaluation of the Value of Mammaprint Test Gene Variation in the Prediction of Neoadjuvant Chemotherapy for Breast Cancer

NCT number NCT04264468
Study type Observational
Source Zhejiang Cancer Hospital
Contact Xing fei Yu, doctoral degree
Phone +86-13588164600
Email yuxf1177@zjcc.org.cn
Status Recruiting
Phase
Start date May 14, 2019
Completion date March 1, 2021