跳至主要内容
临床试验/NCT00907140
NCT00907140已完成不适用

Assessment of Changes in Pattern and Magnitude of Tumor FDG Uptake During Chemoradiation as a Predictor of Response to Concurrent Radiation Therapy and Chemotherapy in Patients With Cervical Cancer

Washington University School of Medicine1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2008年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
25
试验地点
1
主要终点
The overall goal of this pilot study is to evaluate the change in cervical tumor FDG heterogeneity and SUVmax during chemoradiation.

研究概览

简要总结

Rationale: Diagnostic procedures, such as positron emission tomography (PET) using fluorodeoxyglucose (FDG), may help determine response to standard cancer therapy in patients with cervical cancer

The purpose of this study is to evaluate the change in cervical tumor heterogenity as measured by FDG-PET/CT imaging.

研究设计

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

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Biopsy-proven cervical cancer. (FIGO stage-Ib2-IVa)
  • •Able to receive chemoradiation therapy with Cisplatin.
  • •Non-pregnant status in women of childbearing potential.
  • •No other active cancer at the time of diagnosis of cervical cancer Patients cannot have received treatment for any malignancy, with the exception of non-melanoma skin cancer, in the past 5 years.
  • •Patients with distant metastatic disease are eligible provided the estimated survival of the patient is at least 1 year.
  • •Scheduled to undergo or have already undergone FDG-PET/CT imaging for clinical staging of cervical cancer at Barnes-Jewish Hospital Clinical PET Facility on a Biograph 40 PET/CT scanner
  • •Able to give informed consent

排除标准

  • •Patients with a known active malignancy other than cervical carcinoma.
  • •Pregnant and breastfeeding patients.
  • •Subjects whose tumors are not FDG avid on baseline standard of care FDG-PET/CT imaging

研究组 & 干预措施

Chemoradiation therapy

Other

干预措施: Positron Emission Tomography (Procedure)

结局指标

主要结局

The overall goal of this pilot study is to evaluate the change in cervical tumor FDG heterogeneity and SUVmax during chemoradiation.

时间窗: FDG PET/CT imaging is performed at: Baseline, 2 & 4 weeks of therapy, and 3 months after completing therapy

次要结局

  • To correlate changed in FDG heterogeneity and SUVmax with response to therapy.(5 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Farrokh Dehdashti

Co-Principal Investigator

Washington University School of Medicine

研究点 (1)

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