HPB
Michael A. Turner, MD
Surgery resident
University of California, San Diego
San Diego, California, United States
Disclosure: Disclosure information not submitted.
Nude mice received surgical orthotopic implantation (SOI) of human pancreatic-cancer cell-line BxPC-3 expressing green fluorescent protein (GFP)s. An anti-carcinoembryonic antigen-related cell adhesion molecule (CEACAM) monoclonal antibody (6G5j) was conjugated to IR700DX (6G5j-IR700DX). Three weeks after SOI, 16 mice received 50μg 6G5j-IR700DX via tail-vein injection 24 hours before surgery and were randomized to two groups: FGS-only (n=8) and FGS + PIT (n=8). All tumors were imaged with the Pearl Trilogy Imaging system and resected under the guidance of the FLARE Imaging System with merged 700 nm and bright-light channels (Figure). The FGS + PIT group received PIT of the surgical bed at an intensity of 150 mW/cm2 for 30 min. Mice were sacrificed 4 weeks after initial surgery and tumors were imaged with a Dino-Lite digital microscope, excised, and weighed.
Results:
6G5j-IR700DX brightly illuminated the orthotopic pancreatic tumors for FGS and PIT. The local recurrence rate was 100.0 % for FGS-only and 50.0 % for the combination of FGS + PIT (p = 0.077). The metastatic recurrence rate was 100.0 % for FGS-only and 25.0 % for FGS + PIT (p = 0.007). The average total recurrent tumor weight was 2370.3 ± 1907.8 mg for FGS-only and 705.5 ± 1200.0 mg for FGS + PIT (p = 0.039).
Conclusions:
FGS and adjuvant PIT can be combined by using a single antibody-fluorophore conjugate (6G5j-IR700DX). In this study, FGS combined with PIT could significantly reduce the frequency of metastatic recurrence and the total weight of recurrent tumors of pancreatic cancer.