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临床试验/NCT04264468
NCT04264468Unknown不适用

Correlation Between Molecular Typing and Neoadjuvant Chemotherapy in Breast Cancer Patients Based on Mammaprint/Blueprint Test

Zhejiang Cancer Hospital1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2019年5月14日最近更新:
适应症

试验速览

阶段
不适用
入组人数
150
试验地点
1
主要终点
Recurrence Score variation after neoadjuvant chemotherapy

研究概览

简要总结

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.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Retrospective

入排标准

年龄范围
25 Years 至 80 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Pathologically confirmed new breast cancer (invasive cancer)
  • Clinical stage II-III
  • Aged 25-80
  • At least 6 months of follow-up data, clinical diagnosis and treatment information and personal information available for follow-up are complete
  • Complete biological samples required for the study: fresh/frozen tissues/white tablets/wax blocks meeting the requirements of the experiment (before neoadjuvant chemotherapy)
  • Tumor markers and imaging data were complete
  • Neoadjuvant chemotherapy is commonly recommended by the standard NCCN guidelines

排除标准

  • Subjects refuse to participate
  • First diagnosis of stage I or IV breast cancer
  • Pathological diagnosis of concurrent (or previous) other malignant tumors
  • Prehistory breast cancer
  • Younger than 25 or older than 80
  • Clinical diagnosis and treatment information or biological samples required by the research institute do not meet the needs of the experiment

结局指标

主要结局

Recurrence Score variation after neoadjuvant chemotherapy

时间窗: 6 months

The recurrence score of each subtype

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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