跳至主要内容
临床试验/NCT03065790
NCT03065790终止不适用

Early FDG PET/CT Imaging as a Measure of Response in Patients With Non-Hodgkin Lymphoma on Lenalidomide

Abramson Cancer Center at Penn Medicine1 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2017年2月6日最近更新:
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
1
主要终点
Number of FDGmax SUV % change in FDG SUVmax

研究概览

简要总结

Adult patients with non-Hodgkin lymphoma who will be treated with lenalidomide will undergo FDG PET/CT scan as an early evaluation of response to therapy. Changes in FDG uptake will be correlated response and long term outcomes.

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

入选标准

  • Adult patients, at least 18 years of age
  • History of histologically confirmed NHL as assessed per medical record review.
  • At least one site of measurable disease (per RECIST 1.1) that is seen on CT, MRI, or FDG PET/CT.
  • Recommended to start lenalidomide.
  • Participants must be informed of the investigational nature of this study and provide written informed consent in accordance with institutional and federal guidelines prior to study-specific procedures.

排除标准

  • Females who are pregnant or breast-feeding at the time of screening will not be eligible for this study. Female participants of child-bearing potential will have a urine or serum pregnancy test at the time of the screening visit.
  • Inability to tolerate imaging procedures in the opinion of the investigator or treating physician.
  • Serious or unstable medical or psychological conditions that, in the opinion of the investigator would compromise the subject's safety or successful participation in the study.

结局指标

主要结局

Number of FDGmax SUV % change in FDG SUVmax

时间窗: 2 years

次要结局

  • Overall Survival(2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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