PMID- 36212472 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20221012 IS - 2234-943X (Print) IS - 2234-943X (Electronic) IS - 2234-943X (Linking) VI - 12 DP - 2022 TI - Synthetic CT generation for MRI-guided adaptive radiotherapy in prostate cancer. PG - 969463 LID - 10.3389/fonc.2022.969463 [doi] LID - 969463 AB - Current MRI-guided adaptive radiotherapy (MRgART) workflows require fraction-specific electron and/or mass density maps, which are created by deformable image registration (DIR) between the simulation CT images and daily MR images. Manual density overrides may also be needed where DIR-produced results are inaccurate. This approach slows the adaptive radiotherapy workflow and introduces additional dosimetric uncertainties, especially in the presence of the magnetic field. This study investigated a method based on a conditional generative adversarial network (cGAN) with a multi-planar method to generate synthetic CT images from low-field MR images to improve efficiency in MRgART workflows for prostate cancer. Fifty-seven male patients, who received MRI-guided radiation therapy to the pelvis using the ViewRay MRIdian Linac, were selected. Forty-five cases were randomly assigned to the training cohort with the remaining twelve cases assigned to the validation/testing cohort. All patient datasets had a semi-paired DIR-deformed CT-sim image and 0.35T MR image acquired using a true fast imaging with steady-state precession (TrueFISP) sequence. Synthetic CT images were compared with deformed CT images to evaluate image quality and dosimetric accuracy. To evaluate the dosimetric accuracy of this method, clinical plans were recalculated on synthetic CT images in the MRIdian treatment planning system. Dose volume histograms for planning target volumes (PTVs) and organs-at-risk (OARs) and dose distributions using gamma analyses were evaluated. The mean-absolute-errors (MAEs) in CT numbers were 30.1 +/- 4.2 HU, 19.6 +/- 2.3 HU and 158.5 +/- 26.0 HU for the whole pelvis, soft tissue, and bone, respectively. The peak signal-to-noise ratio was 35.2 +/- 1.7 and the structural index similarity measure was 0.9758 +/- 0.0035. The dosimetric difference was on average less than 1% for all PTV and OAR metrics. Plans showed good agreement with gamma pass rates of 99% and 99.9% for 1%/1 mm and 2%/2 mm, respectively. Our study demonstrates the potential of using synthetic CT images created with a multi-planar cGAN method from 0.35T MRI TrueFISP images for the MRgART treatment of prostate radiotherapy. Future work will validate the method in a large cohort of patients and investigate the limitations of the method in the adaptive workflow. CI - Copyright (c) 2022 Hsu, Han, Leeman, Hu, Mak and Sudhyadhom. FAU - Hsu, Shu-Hui AU - Hsu SH AD - Department of Radiation Oncology, Brigham and Women's Hospital and Dana-Farber Cancer Institute, Boston, MA, United States. FAU - Han, Zhaohui AU - Han Z AD - Department of Radiation Oncology, Brigham and Women's Hospital and Dana-Farber Cancer Institute, Boston, MA, United States. FAU - Leeman, Jonathan E AU - Leeman JE AD - Department of Radiation Oncology, Brigham and Women's Hospital and Dana-Farber Cancer Institute, Boston, MA, United States. FAU - Hu, Yue-Houng AU - Hu YH AD - Department of Radiation Oncology, Brigham and Women's Hospital and Dana-Farber Cancer Institute, Boston, MA, United States. FAU - Mak, Raymond H AU - Mak RH AD - Department of Radiation Oncology, Brigham and Women's Hospital and Dana-Farber Cancer Institute, Boston, MA, United States. FAU - Sudhyadhom, Atchar AU - Sudhyadhom A AD - Department of Radiation Oncology, Brigham and Women's Hospital and Dana-Farber Cancer Institute, Boston, MA, United States. LA - eng GR - R21 EB026086/EB/NIBIB NIH HHS/United States PT - Journal Article DEP - 20220923 PL - Switzerland TA - Front Oncol JT - Frontiers in oncology JID - 101568867 PMC - PMC9539763 OTO - NOTNLM OT - MRI-guided therapy OT - adaptive radiotherapy OT - deep learning OT - prostate radiotherapy OT - synthetic CT COIS- JL has received research funding from ViewRay and NH TherAguix. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. EDAT- 2022/10/11 06:00 MHDA- 2022/10/11 06:01 PMCR- 2022/01/01 CRDT- 2022/10/10 04:12 PHST- 2022/06/15 00:00 [received] PHST- 2022/08/26 00:00 [accepted] PHST- 2022/10/10 04:12 [entrez] PHST- 2022/10/11 06:00 [pubmed] PHST- 2022/10/11 06:01 [medline] PHST- 2022/01/01 00:00 [pmc-release] AID - 10.3389/fonc.2022.969463 [doi] PST - epublish SO - Front Oncol. 2022 Sep 23;12:969463. doi: 10.3389/fonc.2022.969463. eCollection 2022.