Perfusion CT as a Predictor of Treatment Response in Patients With Rectal Cancer



Status:Completed
Conditions:Colorectal Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:9/9/2018
Start Date:November 2011
End Date:July 2018

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A research study of rectal cancer perfusion (how blood flows to the rectum over time). We
hope to learn whether perfusion characteristics of rectal masses may be predictive of
response to treatment and whether rectal perfusion characteristics can be used to follow
response to treatment.

Recent advances in computed tomography (CT) technology have made CT perfusion imaging
feasible for the assessment of tumor perfusion in solid tumors of the abdomen. CT perfusion
has shown promising results in serving as a noninvasive method of predicting response to
therapy in cancer patients. CT perfusion parameters have also been found to correlate with
immunohistologic markers of angiogenesis in a number of solid tumors, suggesting a possible
role for CT perfusion as a noninvasive biomarker of tumor angiogenesis. The goals of the
investigators study are twofold: first, to determine the relationship between baseline CT
perfusion characteristics of rectal cancers and their response to treatment, and second, to
determine if perfusion CT can be used to subsequently monitor tumor response to treatment.
The investigators hope to enroll those patients with locally advanced rectal cancer
undergoing standard CT for pre-treatment planning, integrating CT perfusion imaging into the
current abdomen/pelvis imaging protocol with close clinical and radiologic follow-up after
treatment to determine response to therapy and time to disease progression.

Inclusion Criteria:

- Patients with suspected or biopsy-proven, locally advanced rectal cancer will be
eligible for enrollment.

- Patients must be 18 years or older. Patients must not be pregnant and, if of
child-bearing age, must take precautions not to become pregnant.

- No life expectancy restrictions.

- ECOG and Karnofsky Performance Status will not be employed.

- Patients with renal failure are ineligible for this study (GFR must be > 60)

- Ability to understand and willingness to sign a written informed consent document.

Exclusion Criteria:

- Patients who have undergone prior treatment for rectal cancer are ineligible for
enrollment.

- No restrictions regarding use of other investigational agents.

- Patients with severe contrast allergy are ineligible.

- Patients who are pregnant or are trying to become pregnant are excluded from this
study.

- Patients who are cancer survivors or HIV-positive will not be excluded.
We found this trial at
1
site
291 Campus Dr
Stanford, California 94305
(650) 725-3900
Stanford University School of Medicine Vast in both its physical scale and its impact on...
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mi
from
Stanford, CA
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