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临床试验/NCT05192642
NCT05192642已完成不适用

Comparative Effectiveness Study of Real-world Control of TRK Fusion Positive Cancer With Patients From Larotrectinib (Vitrakvi) Clinical Trials

Bayer1 个研究点 分布在 1 个国家目标入组 368 人开始时间: 2021年12月3日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
Bayer
入组人数
368
试验地点
1
主要终点
Overall survival (OS)

研究概览

简要总结

This is an observational study in which patient data from the past of adult people with solid tumors harboring NTRK gene fusion are studied. This study will focus on 5 tumor types which have been at the late stage or have spread to other parts of the body. These 5 tumor types are:

  • Non-small-cell-lung cancer
  • Colorectal cancer (located in the intestine)
  • Thyroid cancer
  • Sarcomas (located in the connective tissue like bones or body fat)
  • Salivary gland carcinoma

In some people with cancer, the cancer cells have specific changes in their building plans (genes) called NTRK gene fusion. NTRK stands for neurotrophic tyrosine receptor kinase, the specific gene that is changed. Due to this change in the gene, an altered protein known as a TRK fusion protein is made, which can cause cancer cells to grow and survive. While NTRK is the gene, TRK (tropomyosin receptor kinase) is the name of the protein. The specific cancer is therefore also called TRK fusion-positive cancer.

The study drug, larotrectinib works by blocking the altered TRK fusion protein. Larotrectinib is already available in the US, Europe, and in other countries and is approved for doctors to prescribe to patients with TRK fusion cancer.

The main purpose of this study is to learn more about how well larotrectinib works in adults with TRK fusion-positive cancer compared to other treatments. Researchers will compare how long participants who received larotrectninib lived to how long participants who received other treatments lived. To do this, larotrectinib data from past clinical studies will be compared with data on other treatments gathered from different health data sources. The data will cover the time between January 2013 and end of August 2022.

Besides this data collection, no further tests or examinations are planned and no visits are required in this study.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

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

  • Diagnosis of advanced stage of disease or metastatic disease.

排除标准

  • Patients involved in TRK inhibitor clinical trials will be excluded from RW control cohort.

研究组 & 干预措施

Larotrectinib clinical trial cohort

干预措施: Larotrectinib(Vitrakvi, BAY2757556) (Drug)

RW external comparator cohort

干预措施: Data on other treatments (Drug)

结局指标

主要结局

Overall survival (OS)

时间窗: Retrospective analysis from January 2013 to August 2022

次要结局

  • Overall Treatment patterns(Retrospective analysis from January 2013 to August 2022)

研究者

发起方
Bayer
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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