This phase I/II trial tests how well second window imaging using indocyanine green (ICG) (TumorGlow [trademark] central nervous system [CNS]) identifies tumor tissue from normal tissue in patients during surgery for brain or spine (nervous system) tumors. In addition to primary brain tumors, many other types of cancers spread to the brain and may require surgery to remove. Near infrared (NIR) imaging uses wavelengths in the infrared range to directly visualize tissue. ICG is a dye that causes tumor tissue to glow when used with the NIR imaging system. Using ICG with NIR imaging during surgery may improve identification of tumor tissue from normal tissue resulting in improved resection of the tumor in patients with nervous system tumors.
Additional locations may be listed on ClinicalTrials.gov for NCT05746104.
Locations matching your search criteria
United States
Pennsylvania
Philadelphia
University of Pennsylvania/Abramson Cancer CenterStatus: Active
Contact: John Young K. Lee
Phone: 215-200-3012
PRIMARY OBJECTIVES:
I. To optimize same day dosing and timing of indocyanine green (ICG) for visualization of contrast-enhancing brain tumors by measuring tumor near-infrared (NIR) signal. (Part 1)
II. To determine the effect a tumor fluorophore has in surgical decision-making during brain tumor surgery. (Part 2)
III. To calculate true positives, by correlating “equivocal tissue” specimens which are positive in NIR with pathology. (Part 2)
SECONDARY OBJECTIVES:
I. To evaluate safety and toxicity, including review of vital signs and any reported or observed adverse events (AEs). (Part 1)
II. Using the recorded changes in resection decision based on NIR fluorescence after white light, to evaluate the pathological efficacy of changes in resection decision to no changes in decision. (Part 2)
III. Of all resected specimens, to compare the test accuracy of the surgeon’s identification of “likely tumor” and “unlikely tumor” under white light to the accuracy of “fluorescent” and “non-fluorescent” under NIR. (Part 2)
IV. To evaluate safety and toxicity, including review of vital signs and any reported or observed adverse events (AEs). (Part 2)
OUTLINE:
Patients receive ICG intravenously (IV) at induction of anesthesia prior to standard of care surgery and undergo NRI imaging on study. Patients also receive ICG injection at resected tissue margin and NRI imaging for further inspection and may undergo additional resection of remaining tumor tissue on study.
Lead OrganizationUniversity of Pennsylvania/Abramson Cancer Center
Principal InvestigatorJohn Young K. Lee