TY - JOUR T1 - A Patient-Derived Orthotopic Xenograft Model of Gastroesophageal-Junction Adenocarcinoma Translated to the Clinic by Tumor-Targeting Fluorescent Antibodies to Carcinoembryonic-Antigen-Related Cell-Adhesion Molecules JF - In Vivo JO - In Vivo SP - 1959 LP - 1963 DO - 10.21873/invivo.12463 VL - 35 IS - 4 AU - MICHAEL A. TURNER AU - SIAMAK AMIRFAKHRI AU - HIROTO NISHINO AU - THINZAR M. LWIN AU - THOMAS J. SAVIDES AU - TONY R. REID AU - BERNHARD B. SINGER AU - ROBERT M. HOFFMAN AU - MICHAEL BOUVET Y1 - 2021/07/01 UR - http://iv.iiarjournals.org/content/35/4/1959.abstract N2 - Background/Aim: During surgical resection of gastroesophageal-junction (GEJ) adenocarcinoma, the margin status is often difficult to visualize resulting in high recurrence rates. The aim of the present study was to develop a labelling technique that would allow improved visualization of GEJ tumor margins for surgeons to reduce recurrence rates in a patient-like model. Materials and Methods: A patient GEJ tumor was obtained from an endoscopic biopsy and implanted subcutaneously in a nude mouse. A patient-derived orthotopic xenograft (PDOX) model was established by implanting tumor fragments grown from a subcutaneous model to the cardia of the stomach of nude mice. CC1/3/5-SAB, an antibody to carcinoembryonic-antigen-related cell-adhesion molecules, was conjugated with infrared dye IRDye800 to create SAB-IR800. Forty-eight hours after i.v. injection of SAB-IR800, GEJ-PDOX mice were imaged. Results: Fluorescence imaging with SAB-IR800 brightly visualized the GEJ adenocarcinoma demonstrating specific targeting. In the PDOX model, injection of SAB-IR800 (50 μg) resulted in a tumor to background ratio of 1.78 at 48 hours and 1.86 at 72 hours. Conclusion: PDOX models of GEJ tumors can be established from patients by endoscopic biopsy without undergoing surgical resection. GEJ PDOX models should be useful for developing novel diagnostics and therapeutics for this recalcitrant disease. ER -