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临床试验/NCT05522881
NCT05522881招募中不适用

The Registry Study of Genetic Alterations of Oropharyngeal Cancer in Taiwan

National Health Research Institutes, Taiwan7 个研究点 分布在 1 个国家目标入组 410 人开始时间: 2022年11月25日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
410
试验地点
7
主要终点
To enroll a total of 300 patients with OPSCC who fit the criteria of this study in the enrolled period

研究概览

简要总结

We will use the next-generation sequencing (NGS) technology to identify genomic alterations of Taiwanese HPV positive and negative oropharyngeal squamous cell carcinoma (OPSCC) for novel biomarker development and the study design of potential clinical trials or translational research.

详细描述

In the past decade, next-generation sequencing (NGS) technology has enabled cancer genome sequencing in screening and searching for new cancer genes in an efficient manner. This massive sequencing technique not only help to identify new altered genes for novel biomarker development, but also reveal gene alterations sensitive or resistant to specific therapies. Because the difference of genomic profiling between Taiwanese HPV positive and negative OPSCC is not clear yet, we propose this multi-center research project to address this issue. In this study, we will collect tumor tissues and clinical information from patients with OPSCC and create a platform for data storage and sharing.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Other

入排标准

年龄范围
20 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Ages 20 and above
  • Pathological reported as squamous cell carcinoma of head and neck
  • Available p16 immunohistochemical staining status (restricted to the OPSCC subgroup)
  • Participants have both archival tumor tissues from the primary head and neck SCC and from the first recurrent tumor (for the recurrence subgroup)
  • Recurrence status is defined as the reappearance of the disease occurring more than 6 months following curative surgery and/or chemoradiotherapy in the recurrence subgroup
  • Willingness to provide archival or newly obtained tumor tissues for current study proposal
  • Life expectancy more than 3 months
  • Patients fully understand the protocol with the willingness to have regular follow-up

排除标准

  • Inability to cooperate by providing a complete medical history
  • No available tumor tissues for genetic testing
  • Undesirable compliance
  • Having a known additional malignancy that is progressing or has required active treatment within the past 3 years. Participants with basal cell carcinoma of the skin, squamous cell carcinoma of the skin, or carcinoma in situ (e.g., cervical carcinoma in situ) that have undergone potentially curative therapy are not excluded

结局指标

主要结局

To enroll a total of 300 patients with OPSCC who fit the criteria of this study in the enrolled period

时间窗: 5 years of proposed observation period

To enroll a total of 300 patients with OPSCC who fit the criteria of this study in the enrolled period

次要结局

  • To compare the difference of the genetic and molecular profiles among patients with HPV positive and negative OPSCC(5 years of proposed observation period)
  • To compare the difference of genetic and molecular profiles between early (stage I and II) and advanced stage (stage III and IV) of HPV positive OPSCC(5 years of proposed observation period)
  • To perform next generation sequencing analysis of OPSCC tumor tissues(5 years of proposed observation period)
  • Collect clinical data of OPSCC(5 years of proposed observation period)

研究者

发起方
National Health Research Institutes, Taiwan
申办方类型
Other
责任方
Sponsor

研究点 (7)

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