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临床试验/NCT05221372
NCT05221372招募中不适用

proSpecTive sAmpling in dRiver muTation Pulmonary Oncology Patients on Tyrosine Kinase Inhibitors

Erasmus Medical Center1 个研究点 分布在 1 个国家目标入组 1,300 人开始时间: 2017年2月2日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
1,300
试验地点
1
主要终点
Plasma concentrations of the small molecule kinase inhibitor during treatment until progression of disease

研究概览

简要总结

The study is perfomed with adult patients with non-small cell lung cancer treated with tyrosine kinase inhibitor. The objective is to collect repeated samples of blood from patients (starting) on a tyrosine kinase inhibitor, for liquid mutation testing, and pharmacokinetic analysis.

详细描述

This is an observational study in pulmonary oncology patients treated with TKI. Ideally before start of therapy, at week 4, 8 12, and then every 4-8 weeks (following the standard of care clinical pathways local guidelines) extra tubes of blood will be collected during blood withdrawal planned for standard-of-care. When a TKI switch takes place, patients receive a new study number and the blood collection will be continued following standard-of-care. Sampling will be performed during steady-state in working hours before next ingestion of TKI (the regular morning dose will need to be postponed until after blood withdrawal).

The moment of blood withdrawal after start of therapy and after last dosage of TKI will be registered.

At the time of progression the current standard of care is to perform a rebiopsy, to identify the resistance mechanism and determine the next appropriate systemic therapy for a patient. Some mechanisms can only be determined on a biopsy specimen (e.g. transformation to SCLC, MET amplification FISH). This study is observational and will not interfere with the current standard practice, therefore the treating physician is free to determine the indication for and possibility of a rebiopsy. However, when a biopsy is taken as standard of care, we will also draw an extra blood sample on the day of the biopsy (preferably during standard preprocedural coagulation status laboratory investigations) and use a portion of the biopsy for a fresh frozen specimen, as evolving molecular investigations (like RNA analysis) often need fresh non-fixed material to obtain reliable results.

Four to five core biopsies will be obtained for further analysis. Half of the obtained biopsy material will be stored in formalin according to local standard procedures, while the other half will be fresh frozen according to local standard procedures and stored for further analysis.

When the treating physician needs to take additional tissue or liquid (e.g. pleural fluid, liquor) for investigations following standard-of-care protocols, we would like to perform additional molecular and/or pharmacokinetic analysis on the residual material when applicable.

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
  • Able to understand the written informed and able to give informed consent
  • Locally advanced or metastatic NSCLC with oncogenic driver mutation
  • Treatment with TKI according to standard of care

排除标准

  • Unable to draw blood for study purposes

结局指标

主要结局

Plasma concentrations of the small molecule kinase inhibitor during treatment until progression of disease

时间窗: 10 years

Describing the plasma concentrations over time during treatment with a small molecule kinase inhibitor by sequentially measuring mean concentrations of the small molecule kinase inhibitor.

Relative presence of primary mutation and resistance mutations in plasma levels under treatment of a small molecule kinase inhibitor until progression of disease measured in variant allele frequency

时间窗: 10 years

Describing the plasma levels of primary mutations and resistance mutations under treatment by sequentially measuring cell free tumor DNA. Different techniques will be used for the plasma mutation detection (ddPCR and NGS)

次要结局

  • Correlation of mutation status in blood to (re)biopsy specimen results performed for standard-of-care.(10 years)
  • Correlation between the BMI of the patient and mean concentration of the small molecule kinase inhibitor(10 years)
  • Correlation between smoking status of the patients and mean concentration of the small molecule kinase inhibitor(10 years)
  • Overall survival(10 years)
  • Pharmacokinetics of intratumoral small molecule kinase inhibitors(10 years)
  • Time to progression or death under treatment with small molecule kinase inhibitor(10 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Anne-Marie Dingemans

MD, PhD

Erasmus Medical Center

研究点 (1)

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