Abstract

BackgroundThe rabbit VX2 lung cancer model is a large animal model useful for preclinical lung cancer imaging and interventional studies. However, previously reported models had issues in terms of invasiveness of tumor inoculation, control of tumor aggressiveness and incidence of complications.PurposeWe aimed to develop a minimally invasive rabbit VX2 lung cancer model suitable for imaging and transbronchial interventional studies.MethodsNew Zealand white rabbits and VX2 tumors were used in the study. An ultra-thin bronchoscope was inserted through a miniature laryngeal mask airway into the bronchus. Different numbers of VX2 tumor cells were selectively inoculated into the lung parenchyma or subcarinal mediastinum to create a uniform tumor with low incidence of complications. The model was characterized by CT, FDG-PET, and endobronchial ultrasound (EBUS). Liposomal dual-modality contrast agent was used to evaluate liposome drug delivery system in this model.ResultsBoth peripheral and mediastinal lung tumor models were created. The tumor making success rate was 75.8% (25/33) in the peripheral lung tumor model and 60% (3/5) in the mediastinal tumor model. The group of 1.0×106 of VX2 tumor cells inoculation showed a linear growth curve with less incidence of complications. Radial probe EBUS visualized the internal structure of the tumor and the size measurement correlated well with CT measurements (r2 = 0.98). Over 7 days of continuous enhancement of the lung tumor by liposomal contrast in the lung tumor was confirmed both CT and fluorescence imaging.ConclusionOur minimally invasive bronchoscopic rabbit VX2 lung cancer model is an ideal platform for lung cancer imaging and preclinical bronchoscopic interventional studies.

Highlights

  • Lung cancer is the leading cause of cancer-related death in the Western world accounting for 28% of all cancer deaths

  • Our minimally invasive bronchoscopic rabbit VX2 lung cancer model is an ideal platform for lung cancer imaging and preclinical bronchoscopic interventional studies

  • Recent clinical trials suggest that annual low dose x-ray computed tomography (CT) screening increases the incidence of lung cancer cases while decreasing the number of mortality [1]

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Summary

Introduction

Lung cancer is the leading cause of cancer-related death in the Western world accounting for 28% of all cancer deaths. Liposomebased contrast agents have shown to successfully accumulate in tumors and provide prolonged signal enhancement of target lesions [4] These are most suitable for applications which require longitudinal and repeated imaging such as image-guided surgical interventions. For successful clinical translation and validation of new imaging and endobronchial intervention tools, a reproducible lung cancer model in a larger animal is required. This type of model should provide a comparable setting to that of a human in order to allow for evaluation of the changes in both the objective tumor and the surrounding tissues and organs pre, during and posttreatment. Previously reported models had issues in terms of invasiveness of tumor inoculation, control of tumor aggressiveness and incidence of complications.

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