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 (OS-TUMOVASC)
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.
研究概览
研究类型
注册 (预期的)
联系人和位置
学习地点
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Lorraine
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Vandoeuvre-lès-Nancy、Lorraine、法国、54500
- Seitlinger
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
描述
Inclusion Criteria:
- 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
Exclusion Criteria:
- Refusal to participate
- Hepatitis
- HIV
- Legal guardianship
- Guardianship
- Inability to give informed information to the patient
- Pregnant women-
学习计划
研究是如何设计的?
设计细节
队列和干预
团体/队列 |
干预/治疗 |
|---|---|
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General cohorte
patient with non-small cell lung cancer undergoing surgical resection in the thoracic surgery department of the Nancy CHRU
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collection of a fragment of healthy and tumorous lung tissue taken as part of the operating theatre procedure and normally destined to be destroyed
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Evaluation of the in vitro efficacy of osimertinib in a patient-derived organoid model alone or in combination
大体时间:from day 0 to day 30
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Cell viability test
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from day 0 to day 30
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Identify non-responders to osimertinib in vitro
大体时间:from day 0 to day 30
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Cell viability test
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from day 0 to day 30
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (预期的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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