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临床试验/NCT04750122
NCT04750122
招募中
1 期

Neoadjuvant Therapy Study Guided by Drug Screening in Vitro Patient-derived Tumor-like Cell Clusters for HER2 Positive Early Breast Cancer Patients

Peking University People's Hospital1 个研究点 分布在 1 个国家目标入组 46 人2021年3月28日

概览

阶段
1 期
干预措施
neoadjuvant chemotherapy upon in vitro PTC drug sensitivity screenning
疾病 / 适应症
HER2-positive Early Breast Cancer
发起方
Peking University People's Hospital
入组人数
46
试验地点
1
主要终点
pathological complete response(pCR)
状态
招募中
最后更新
5年前

概览

简要总结

Neoadjuvant treatment is an important treatment for early breast cancer patients. Patients with her2 enriched subtype who achieved pCR after neoadjuvant treatment would have longer survival. The neoadjuvant treatment for her2 positive patients include chemotherapy and targeted therapy. Although the pCR rate was high to 60% after use of trastuzumab and pertuzumab, but the adverse reaction of combined chemotherapy could not be negligible. Some studies have attempted chemotherapy-free treatment for her2 positive patients during neoadjuvant therapy. But, which patient could be exempted from chemotherapy and which drug could be omitted are still unknow before treatment. Drug sensitivity screening in vitro was a promising method for choosing chemotherapy. But there was no method could select effective drugs accurately for breast cancer patients until now.

Previously, investigators developed a patient-derived tumor-like cell clusters in vitro culture technology. Feasibility for guiding clinical treatment by drug sensitivity screening based on this technology have been explored by preliminary exploration with a well corresponding. And the results have been published. This study will explore whether drug screening in vitro patient-derived tumor-like cell clusters from breast cancer tissue could be a metheod for omitting chemotherapy for her2 positive participants.

详细描述

Neoadjuvant chemotherapy for breast cancer could make unresectable breast cancer be resectable and improve breast conservation rate. Patients with her2 enriched subtype who achieved pCR after neoadjuvant treatment would have longer survival. The neoadjuvant treatment for her2 positive patients include chemotherapy and targeted therapy. Although the pCR rate was high to 60% after use of trastuzumab and pertuzumab, but the adverse reaction of combined chemotherapy could not be negligible. Based on the application of dual targeted drugs, some studies have attempted chemotherapy-free treatment for her2 positive patients during neoadjuvant therapy. But, which patient could be exempted from chemotherapy and which drug could be omitted are still unknow before treatment. Drug sensitivity screening in vitro was a promising method for choosing chemotherapy. But there was no method could select effective drugs accurately for breast cancer participants until now. Previously, investigators developed a patient-derived tumor-like cell clusters(PTC) in vitro culture technology. It is a cell cluster including tumor cells, mesenchymal cells and lymphocytes, which simulates the tumor microenvironment in vitro. In the preliminary exploration, investigators included 35 early breast cancer participants, the corresponding between in vitro drug sensitivity screening based on this technology and clinical treatment results was well. The results have been published. This study will focus on her2 positive early breast cancer participants. 46 participants will be included. All of them will received in vitro drug sensitivity screenning upon PTC before neoadjuvant therapy. All participants will received trastuzumab and pertuzumab. The choice of chemotherapy drugs is determined based on the PTC drug sensitivity results. If single-agent chemotherapy is effective in vitro, this drug will be the chemotherapy regimen for the corresponding participants. This study expects that the pCR rate could achieve 60% in the case of chemotherapy downgrading after in vitro drug sensitivity screening.

注册库
clinicaltrials.gov
开始日期
2021年3月28日
结束日期
2026年12月31日
最后更新
5年前
研究类型
Interventional
研究设计
Single Group
性别
Female

研究者

责任方
Sponsor

入排标准

入选标准

  • invasive breast cancer
  • HER2 positive
  • T2 or node positive

排除标准

  • inflammatory breast cancer
  • Severe chronic disease

研究组 & 干预措施

Neoadjuvant therapy base on PTC drug screenning

Patients will receive neoadjuvant therapy including trastuzumab, pertuzumab, and chemotherapy based on PTC drug screening.

干预措施: neoadjuvant chemotherapy upon in vitro PTC drug sensitivity screenning

结局指标

主要结局

pathological complete response(pCR)

时间窗: up to 12 weeks

ypT0/is, ypN0

次要结局

  • event-free survival (EFS)(5 years)
  • invasive disease-free survival(IDFS)(5 years)
  • objective response rate(up to 12 weeks)

研究点 (1)

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