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临床试验/NCT02045186
NCT02045186终止不适用

Monitoring of Oral HPV Infection in HPV-positive Oropharyngeal Squamous Cell Carcinoma During and After Chemoradiotherapy (CRT)

UNC Lineberger Comprehensive Cancer Center2 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2013年12月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
1
试验地点
2
主要终点
Proportion of patients with HPV-positive OPSCC undergoing CRT who are clear of their oral HPV infection at each time-point

研究概览

简要总结

The purpose of this research study is to determine whether and when patients with human papilloma virus positive squamous cell cancer of the oropharynx treated with radiation and chemotherapy clear their human papilloma virus infection.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ≥ 18 years of age (no upper age limit)
  • AnyT, AnyN, M0 squamous cell carcinoma of the oropharynx
  • Biopsy proven squamous cell carcinoma that is HPV positive via standard pathological assessment of tumor tissues in pathology department at the treating institution
  • Scheduled for definitive CRT as primary treatment of their oropharynx cancer

排除标准

  • Prior history of radiation therapy to the head and neck
  • Prior history of mucosal head and neck cancer.
  • Not willing or able to comply with study specific procedures

结局指标

主要结局

Proportion of patients with HPV-positive OPSCC undergoing CRT who are clear of their oral HPV infection at each time-point

时间窗: 2 years post-CRT of last enrolled patient

次要结局

  • Time to HPV clearance for patients with HPV-positive OPSCC undergoing CRT(2 years post-CRT of last enrolled patient)
  • Number of aneuploidy cells as measured by FISH (Florescent in-situ hybridization) and the mRNA copy number for HPV E6 and HPV E7 at each time-point(2 years post-CRT of last enrolled patient)
  • Clinical outcomes of interest (local control, loco-regional control, distant metastasis-free survival, and overall survival (OS)) in patients with HPV-positive OPSCC undergoing CRT(2 years post-CRT of last enrolled patient)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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