Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/95641
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Title: Advances in MRI-guided precision radiotherapy
Authors: Liu, C 
Li, M
Xiao, H 
Li, T 
Li, W 
Zhang, J 
Teng, X 
Cai, J 
Issue Date: Mar-2022
Source: Precision radiation oncology, Mar. 2022, v. 6, no. 1, p. 75-84
Abstract: Magnetic resonance imaging (MRI) is becoming increasingly important in precision radiotherapy owing to its excellent soft-tissue contrast and versatile scan options. Many recent advances in MRI have been shown to be promising for MRI-guided radiotherapy and for improved treatment outcomes. This paper summarizes these advances into six sections: MRI simulators, MRI-linear accelerator hybrid machines, MRI-only workflow, four-dimensional MRI, MRI-based radiomics, and magnetic resonance fingerprinting. These techniques can be implemented before, during, or after radiotherapy for various precision radiotherapy applications, such as tumor delineation, tumor motion management, treatment adaptation, and clinical decision making. For each of these techniques, this paper describes its technical details and discusses its clinical benefits and challenges.
Keywords: 4D-MRI
MR-Linac
MRI-guided radiotherapy
Publisher: John Wiley & Sons Ltd.
Journal: Precision radiation oncology 
EISSN: 2398-7324
DOI: 10.1002/pro6.1143
Rights: © 2022 The Authors. Precision Radiation Oncology published by John Wiley & Sons Australia, Ltd on behalf of Shandong Cancer Hospital & Institute.
This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
The following publication Liu, C., Li, M., Xiao, H., Li, T., Li, W., Zhang, J., ... & Cai, J. (2022). Advances in MRI‐guided precision radiotherapy. Precision Radiation Oncology, 6(1), 75-84 is available at https://doi.org/10.1002/pro6.1143.
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