Breast Cancer Organoids
Conditions
Keywords
Drug sensitivity experiment, Resistance mechanism research
Brief summary
Based on the breast cancer organ platform, this experiment establishes a drug sensitivity test method that is closer to the body tumor in breast cancer, provides a basis for the accurate treatment of breast cancer, and discusses the possible mechanism of breast cancer drug resistance.
Interventions
Toremifene citrate tablets
Trastuzumab Injection
Doxorubicin Hydrochloride Injection
Epirubicin hydrochloride injection
Fluorouracil injection
Paclitaxel injection
Gemcitabine injection
Cisplatin injection
Recombinant Human Endostatin Injection
Pirarubicin hydrochloride injection
Pyrrolidine tablets
Ixapilone Injection
Tamoxifen citrate tablets
Vinorelbine tartrate injection
Carboplatin injection
Methotrexate injection
Eribulin mesylate injection
Anastrozole tablets
Letrozole tablets
Exemestane tablets
Fulvestrant injection
Olapani pill
Bevacizumab injection
Apatinib mesylate tablets
Pattozumab injection
Capecitabine tablets
Ear particles
Aidi Injection
Cyclophosphamide injection
Sponsors
Study design
Eligibility
Inclusion criteria
Patients with breast cancer and the largest tumor diameter ≥ 3cm No previous chemotherapy regimen age 18-65 years old Can obtain the tumor tissue specimens required for culture Heart, liver, kidney and bone marrow hematopoietic function is good Know and sign the informed consent form
Exclusion criteria
Pregnant or lactating women Also suffering from other cancer patients There are serious uncontrolled medical diseases or acute infections Those who are known to be allergic to this study drug or a variety of previous drugs The patient cannot understand the purpose of the study or disagree with the requirements of the study. Other investigators believe that patients who are not suitable for this study group
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Detection of cell viability | 8 weeks before neoadjuvant chemotherapy | 1\. The organ-like organ was assayed for cell viability using CellTiter Glo 3D reagent, and the curve was used to obtain a half-inhibitory concentration range. The dose was adjusted according to the half-inhibition concentration range to obtain an accurate half-inhibitory concentration. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Detection of in vitro model drug sensitivity | 8 weeks before neoadjuvant chemotherapy | 2\. In vitro model drug sensitivity: sensitive and insensitive |
| Clinical efficacy assessment according to RECIST criteria | 8 weeks before neoadjuvant chemotherapy | Clinical efficacy evaluation according to RECIST criteria: imaging ultrasonography, histological pathology. |
Countries
China