Assessing Response to Treatment in Non-Hodgkin's Lymphoma Patients Using 64Cu-DOTA-Rituximab PET/CT



Status:Withdrawn
Conditions:Lymphoma
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:January 2012
End Date:December 2015

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Rituximab is an antibody targeted against the CD20 antigen found primarily on B-cells.
Therefore, an imaging agent targeting CD20 expression may provide a more accurate evaluation
of extent of disease and response to therapy than the current standard of care, F-18 FDG
PET/CT.

The main purpose of the study is to investigate a new PET/CT imaging probe for detection and
follow up of lymphoma. Following are the 3 aims of the study: a) Phase I testing in lymphoma
patients of Cu-64 labelled Rituxan for defining normal tracer biodistribution, stability,
pharmacokinetics and radiation dosimetry; b) comparison of Cu-64 Rituxan and F-18 FDG PET/CT
in lymphoma patients; c) evaluation of changes in uptake of Cu-64 Rituxan in response to
rituximab-based treatment in CD20-positive B-cell NHL


Inclusion Criteria:

- Patients must have a diagnosis of CD20-positive B-cell NHL and a staging 18F FDG
PET/CT prior to the 64Cu-DOTA-Rituximab PET/CT

- Patients must understand and voluntarily sign an Informed Consent form after the
contents have been fully explained to them

- Patients must be scheduled for rituximab-based therapy

- Patients must be older than 18-year-old

Exclusion Criteria:

- Patients who cannot complete a PET/CT scan

- Pregnant women

- Patients participating in other research protocols will be excluded from this study
We found this trial at
1
site
875 Blake Wilbur Dr
Stanford, California 94305
(650) 498-6000
Stanford University Cancer Institute The Stanford Cancer Institute (SCI) focuses the world-class expertise of more...
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Stanford, CA
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