Neoadjuvant Therapy Study Guided by Drug Screening in Vitro Patient-derived Tumor-like Cell Clusters for Human Epidermal Growth Factor Receptor 2 (HER2) Negative Early Breast Cancer Patients
概览
- 阶段
- 1 期
- 干预措施
- neoadjuvant chemotherapy upon in vitro PTC drug sensitivity screening for triple negative breast cancer
- 疾病 / 适应症
- HER2-negative 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
- 4年前
概览
简要总结
Neoadjuvant treatment is an important treatment for early breast cancer patients. Patients with triple negative subtype who achieved pCR after neoadjuvant treatment would have longer survival. The neoadjuvant treatment for her2 negative patient was chemotherapy with combined drugs. However, not all patients benefit from chemotherapy but suffer from chemotherapy-related side effects. It was unknown for a patient who could benefit from which drug before chemotherapy. 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 method for selection of chemotherapy for her2 negative participants.
详细描述
Neoadjuvant chemotherapy for breast cancer could make unresectable breast cancer be resectable and improve breast conservation rate. Patients with triple negative subtype who achieved pCR after neoadjuvant treatment would have longer survival. The neoadjuvant treatment for her2 negative patient was chemotherapy with combined drugs. However, not all patients benefit from chemotherapy but suffer from chemotherapy-related side effects. It was unknown for a patient who could benefit from which drug before chemotherapy. 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 negative early breast cancer participants. 46 participants will be included. All of them will received in vitro drug sensitivity screening upon PTC before neoadjuvant therapy. 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.
研究者
入排标准
入选标准
- •invasive breast cancer
- •HER2 negative
- •T2 or node positive
- •Eastern Cooperative Oncology Group(ECOG) 0-1
排除标准
- •inflammatory breast cancer
- •Severe chronic disease
研究组 & 干预措施
Neoadjuvant therapy base on PTC drug screening for triple negative early breast cancer
Patients with triple negative subtype will receive neoadjuvant chemotherapy based on PTC drug screening.
干预措施: neoadjuvant chemotherapy upon in vitro PTC drug sensitivity screening for triple negative breast cancer
Neoadjuvant therapy base on PTC drug screening for luminal like early breast cancer
Patients with luminal like subtype will receive neoadjuvant chemotherapy based on PTC drug screening.
干预措施: neoadjuvant chemotherapy upon in vitro PTC drug sensitivity screening for luminal like breast cancer
结局指标
主要结局
pathological complete response(pCR)
时间窗: up to 24 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 24 weeks)