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临床试验/NCT03777384
NCT03777384进行中(未招募)不适用

EValuating the Safety Of De-escaLated Head and Neck Irradiation in HPV positivE Oropharynx Cancer in Non-smokers/Minimal Smokers

Sanford Health2 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2018年10月12日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
75
试验地点
2
主要终点
The durability of local disease control of de-escalated radiotherapy protocols in the community cancer center setting.

研究概览

简要总结

A prospective, observational study evaluating the durability of local/regional control of previously published de-escalated radiotherapy protocols for patients with P16 positive oropharynx cancers who have minimal nicotine exposure who are not current uses (< 10 pack year smoking history; < 10 year history of any nicotine product [electronic cigarette, chewing tobacco]). Quality of Life measures will also be collected.

详细描述

This is a prospective, single-site, observational study in head and neck cancer participants. The purpose of this study is to provide a systematic platform to analyze, interpret, and track radiation dose de-escalation therapy and associated participant outcomes from treatments identified by these results.

Participants will be asked to complete quality of life questionnaires at regular time points before, during, and after treatment.

研究设计

研究类型
Observational
观察模型
Case Only
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
否

入选标准

  • •Age > 18 years
  • •Histologic confirmation of tumor of the oropharynx
  • •Radiation therapy (de-escalated head and neck irradiation) decision has been made
  • •Human Papilloma Virus (HPV) associated cancer as determined by positive p16 immunohistochemistry
  • •HPV positivity is defined by p16 IHC staining of > 70% of tumor cells (strong and diffuse nuclear and cytoplasmic staining)
  • •For cases that are indeterminate or if p16 testing cannot be accurately performed, HPV positivity can be confirmed by high-risk HPV DNA Testing which covers the following HPV subtypes: 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68
  • •< 10 pack year smoking history OR < 10 year nicotine use history
  • •No current tobacco/nicotine use (including electronic cigarettes and chewing tobacco)
  • •T1-T3, N0-N2 (AJCC8) requiring definitive therapy greater than surgery alone
  • •Ability to provide informed written consent
  • •Willingness to return to Sanford Cancer Center for follow-up
  • •Life expectancy > 12 weeks
  • •ECOG performance status < 3 (Appendix B)
  • •Adequate organ function for chemotherapy and radiotherapy

排除标准

  • •Any of the following because the inclusion criteria require delivery of radiotherapy and chemotherapy which is known to be genotoxic, and is associated with mutagenic and teratogenic effects: pregnant women, nursing women, men or women of childbearing potential who are unwilling to employ adequate contraception.
  • •Prior head and neck radiotherapy
  • •Any factor precluding safe delivery of chemotherapy

结局指标

主要结局

The durability of local disease control of de-escalated radiotherapy protocols in the community cancer center setting.

时间窗: End of treatment to 5 years after end of treatment

Number of participants who remain disease free from the end of treatment to 5 years after treatment.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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