Evaluation of the Response to Tyrosine Kinase Inhibitors in Localized Non-small Cell Lung Cancer (NSCLC) Patients With EGFR Mutation in a Patient-derived Organoid Model
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 200
- 试验地点
- 1
- 主要终点
- Evaluation of the in vitro efficacy of osimertinib in a patient-derived organoid model alone or in combination
研究概览
简要总结
Lung cancer is a major public health problem and remains the leading cause of cancer mortality worldwide. Moreover, in France, it is the 3rd most common cancer in terms of incidence. Its prognosis remains poor despite the emergence of new therapies, notably the Epithelial Growth Factor Receptor (EGFR) specific tyrosine kinase inhibitors which can be used in patients with adenocarcinoma presenting an activating mutation of EGFR.
In addition, a number of questions remain regarding the use of these molecules, including the possibility of combining them with other therapies such as chemotherapy or radiotherapy. In addition, the duration of treatment with tyrosine kinase inhibitors is a matter of debate, mainly in localised forms (ADAURA trial). For this reason, we have proposed tests using TKIs on an in vitro platform based on organoid formation from tumour biopsies of NSCLC patients. This model will allow to test different molecules, in particular osimertinib which is a third generation tyrosine kinase inhibitor. In this way, it will be possible to evaluate in vitro responder patients within a timeframe compatible with the timeframe proposed by the INCA (4-6 weeks).
For non-responders, it will also be possible to screen them in vitro and seek the ideal alternative therapy. This model therefore aims to develop personalised medicine in thoracic oncology and could be used as a decision aid during multidisciplinary consultation meetings.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •age 18 years or older
- •patient affiliated to a social security scheme
- •having given their agreement to participate in the study
- •with non small cell lung cancer of any stage undergoing surgical resection at the Nancy University Hospital
排除标准
- •Refusal to participate
- •Hepatitis
- •Legal guardianship
- •Guardianship
- •Inability to give informed information to the patient
- •Pregnant women-
结局指标
主要结局
Evaluation of the in vitro efficacy of osimertinib in a patient-derived organoid model alone or in combination
时间窗: from day 0 to day 30
Cell viability test
次要结局
- Identify non-responders to osimertinib in vitro(from day 0 to day 30)
研究者
SEITLINGER Joseph
Principal Investigator
Central Hospital, Nancy, France
