An efficient and robust MRI-guided radiotherapy planning approach for targeting abdominal organs and tumours in the mouse

Zhang, Q. et al. (2017) An efficient and robust MRI-guided radiotherapy planning approach for targeting abdominal organs and tumours in the mouse. PLoS ONE, 12(4), e0176693. (doi: 10.1371/journal.pone.0176693) (PMID:28453537) (PMCID:PMC5409175)

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Introduction: Preclinical CT-guided radiotherapy platforms are increasingly used but the CT images are characterized by poor soft tissue contrast. The aim of this study was to develop a robust and accurate method of MRI-guided radiotherapy (MR-IGRT) delivery to abdominal targets in the mouse. Methods: A multimodality cradle was developed for providing subject immobilisation and its performance was evaluated. Whilst CT was still used for dose calculations, target identification was based on MRI. Each step of the radiotherapy planning procedure was validated initially in vitro using BANG gel dosimeters. Subsequently, MR-IGRT of normal adrenal glands with a size-matched collimated beam was performed. Additionally, the SK-N-SH neuroblastoma xenograft model and the transgenic KPC model of pancreatic ductal adenocarcinoma were used to demonstrate the applicability of our methods for the accurate delivery of radiation to CT-invisible abdominal tumours. Results: The BANG gel phantoms demonstrated a targeting efficiency error of 0.56 ± 0.18 mm. The in vivo stability tests of body motion during MR-IGRT and the associated cradle transfer showed that the residual body movements are within this MR-IGRT targeting error. Accurate MR-IGRT of the normal adrenal glands with a size-matched collimated beam was confirmed by γH2AX staining. Regression in tumour volume was observed almost immediately post MR-IGRT in the neuroblastoma model, further demonstrating accuracy of x-ray delivery. Finally, MR-IGRT in the KPC model facilitated precise contouring and comparison of different treatment plans and radiotherapy dose distributions not only to the intra-abdominal tumour but also to the organs at risk. Conclusion: This is, to our knowledge, the first study to demonstrate preclinical MR-IGRT in intra-abdominal organs. The proposed MR-IGRT method presents a state-of-the-art solution to enabling robust, accurate and efficient targeting of extracranial organs in the mouse and can operate with a sufficiently high throughput to allow fractionated treatments to be given.

Item Type:Articles
Additional Information:The authors received funding from Cancer Research UK (; awards C5255/A15935, C5255/A12678, C5255/A15935), the CRUK/EPSRC Cancer Imaging Centre Oxford (awards C2522/A10339, C5255/A16466), The Medical Research Council (GB) (; award MC_PC_12004) and the Kidani Memorial Trust.
Glasgow Author(s) Enlighten ID:Sansom, Professor Owen
Authors: Zhang, Q., Kersemans, V., Beech, J. S., Gilchrist, S., Kinchesh, P., Allen, P. D., Thompson, J., Gomes, A. L., D’Costa, Z., Bird, L., Tullis, I. D.C., Newman, R. G., Corroyer-Dulmont, A., Falzone, N., Azad, A., Vallis, K. A., Sansom, O. J., Muschel, R. J., Vojnovic, B., Hill, M. A., Fokas, E., and Smart, S. C.
College/School:College of Medical Veterinary and Life Sciences > School of Cancer Sciences
Journal Name:PLoS ONE
Publisher:Public Library of Science
ISSN (Online):1932-6203
Copyright Holders:Copyright © 2017 Kersemans et al.
First Published:First published in PLoS ONE 12(4):e0176693
Publisher Policy:Reproduced under a Creative Commons license

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