PROJECT SUMMARY/ABSTRACT
The failure of surgery to provide a long-disease free survival interval to patients with resected pancreatic
cancer is related to the inability to recognize occult tumor foci at metastatic or locoregional sites. For
surgery to be effective, there is a critical need for real-time detection of small, sub-clinical metastases (if
present) and for visualization of the tumor’s invisible infiltration along the boundaries of the planned
resection. The overall objective of this application is to clinically validate the use of a fluorescently labeled
anti-EGFR antibody, panitumumab-IRDye800CW (pan800), for the intraoperative detection of low-volume
(1-3 mm3) pancreatic cancer tumor foci in vivo. The central hypothesis is that Near InfraRed (NIR)
intraoperative imaging with pan800 will enable ultrasensitive detection of tumor deposits that would
otherwise escape detection using current imaging technology and surgical inspection/palpation. In the
proposed study, patients with pancreatic adenocarcinoma eligible for surgery will undergo infusion of
pan800 2-5 days prior to surgery and NIR cameras will be used intraoperatively to detect 1-3 mm³ tumor
foci. The following two specific aims will be pursued: 1) Determine the diagnostic accuracy of pan800
intraoperative fluorescent imaging to detect radiographically occult (i.e., unseen by the radiologist)
pancreatic adenocarcinoma metastases; and 2) Determine the efficacy of pan800 fluorescent imaging to
identify visibly occult (i.e., unseen by the surgeon) residual tumor foci at the post-surgical resection bed in
vivo or at the margin of the resected specimen ex vivo. Under the first aim, the sensitivity and specificity of
this intraoperative imaging modality to identify small, sub-radiologic peritoneal metastases will be
documented. For the second aim, the incremental yield of this modality over conventional bright-field
inspection in identifying otherwise invisible tumor foci at the resection bed or specimen margin will be
demonstrated. The repurposing of readily available therapeutic EGFR antibodies to surgical imaging agents
is not only safe and cost effective, but also highly innovative, in the applicant’s opinion, as it can challenge
the status quo related to intraoperative pancreatic cancer detection, which has not fundamentally changed
over several decades. The proposed research is significant because it will build upon the previously
demonstrated efficacy of pan800 to detect pancreatic cancer in vivo, providing new opportunities for its
continued development as a tool to enhance intraoperative staging, support decision making, increase the
likelihood of complete tumor resection, and eventually improve clinical outcomes for patients with this highly
lethal malignancy.