跳至主要内容
临床试验/NCT02149641
NCT02149641已完成不适用

Phase II Study of Parotid Sparing IMRT for Nasopharyngeal Cancer

Royal Marsden NHS Foundation Trust1 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2006年2月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
42
试验地点
1
主要终点
the incidence of ≥G2 xerostomia at 1 year using the subjective component LENTSOMA

研究概览

简要总结

In the treatment of nasopharyngeal cancers, to determine the incidence of high grade (≥G2) subjective xerostomia at 1 year.

详细描述

The purpose of this study was to determine the feasibility in delivering induction chemotherapy and concomitant chemotherapy with IMRT in the treatment of locally advanced nasopharyngeal cancers and to determine the incidence of high grade (≥G2) subjective xerostomia at 1 year.

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
16 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • nasopharyngeal cancers

排除标准

  • Patients <16 years old or with a previous malignancy other than non-melanomatous skin cancer were excluded

结局指标

主要结局

the incidence of ≥G2 xerostomia at 1 year using the subjective component LENTSOMA

时间窗: 12 months

次要结局

  • Acute radiation toxicities(0-3 months)
  • loco-regional disease-free survival (LRDFS), progression-free survival (PFS) and overall survival (OS)(2 years)
  • chemotherapy compliance and toxicities(0-12 weeks)
  • Late radiation toxicities(3-24 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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