跳至主要内容
临床试验/NCT02613312
NCT02613312终止不适用

Chemotherapy Followed by Surgery and Neoadjuvant Hemothoracic Intensity Modified Radiation Therapy (IMRT) for Patients With Malignant Pleural Mesothelioma

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2016年3月18日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
Mayo Clinic
入组人数
8
试验地点
1
主要终点
Overall Survival (OS)

研究概览

简要总结

The purpose of this study is to determine the response rate and overall survival in patients that have been diagnosed with mesothelioma and will undergo chemotherapy, surgery and intensity modified radiation therapy (IMRT) as part of their standard of care.

详细描述

The investigators will consent patients that have been diagnosed with mesothelioma and will undergo chemotherapy followed by surgery and then IMRT as their standard of care. The investigators will collect data from past and future medical records as well as data regarding their health status for their lifetime by reviewing life status, treatment status and CT scans.

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

入选标准

  • Subject provides informed consent
  • Subject is >18 years of age
  • Subject is deemed competent for making medical decisions
  • Subject is scheduled to undergo chemotherapy followed by surgery and then IMRT
  • Subject is a surgical candidate
  • A negative pregnancy test is required in women of child-bearing potential, as standard of care.

排除标准

  • Subject is <18 years old.

结局指标

主要结局

Overall Survival (OS)

时间窗: 2 years

OS is defined as the length of time from study enrollment to death by any cause. Survival status of patients will be monitored every 6 months

次要结局

  • Progression free survival (PFS) as evidenced by CT scan review(2 years)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dennis Wigle

Principal Investigator

Mayo Clinic

研究点 (1)

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