Phase I Pilot Study to Evaluate the Prognostic Value of Perfusion CT for Primary Cervical Cancer
| Status: | Completed |
|---|---|
| Conditions: | Cervical Cancer, Cervical Cancer, Cancer, Women's Studies |
| Therapuetic Areas: | Oncology, Reproductive |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 11/2/2018 |
| Start Date: | August 2013 |
| End Date: | October 4, 2018 |
The investigators hope to learn whether perfusion CT is a useful way to assess primary
cervical tumor microenvironment and whether there is a relationship between pretreatment
perfusion CT measurements and primary cervical tumor size, lymph node involvement (as
assessed by standard of care pretreatment fludeoxyglucose Positron emission tomography/CT
(FDG-PET/CT)), and treatment response (as assessed by standard of care 3-month post-therapy
FDG-PET/CT).
cervical tumor microenvironment and whether there is a relationship between pretreatment
perfusion CT measurements and primary cervical tumor size, lymph node involvement (as
assessed by standard of care pretreatment fludeoxyglucose Positron emission tomography/CT
(FDG-PET/CT)), and treatment response (as assessed by standard of care 3-month post-therapy
FDG-PET/CT).
Inclusion criteria:
- >18 years old
- with biopsy-proven squamous, adenocarcinoma or adenosquamous cervical cancer
- no history of prior pelvic radiation and should be able to receive chemoradiation
- non-pregnant women who have not previously undergone a hysterectomy, as that would
have removed the cervix.
- able to give informed consent
Exclusion criteria:
- Subjects whose tumors are not FDG avid on the pre-therapy PET.
- Allergy or inability to receive iodinated CT contrast
We found this trial at
1
site
291 Campus Dr
Stanford, California 94305
Stanford, California 94305
(650) 725-3900
Principal Investigator: Elizabeth Kidd
Phone: 650-723-8843
Stanford University School of Medicine Vast in both its physical scale and its impact on...
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