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临床试验/NCT05136014
NCT05136014Unknown不适用

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

Central Hospital, Nancy, France1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2021年11月1日最近更新:
适应症

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

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

发起方
Central Hospital, Nancy, France
申办方类型
Other
责任方
Principal Investigator
主要研究者

SEITLINGER Joseph

Principal Investigator

Central Hospital, Nancy, France

研究点 (1)

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