| Literature DB >> 36238366 |
So Hee Park1, Dong Min Choi2, In-Ho Jung1, Kyung Won Chang1, Myung Ji Kim3, Hyun Ho Jung1, Jin Woo Chang1, Hwiyoung Kim2,4, Won Seok Chang1.
Abstract
Dose planning for Gamma Knife radiosurgery (GKRS) uses the magnetic resonance (MR)-based tissue maximum ratio (TMR) algorithm, which calculates radiation dose without considering heterogeneous radiation attenuation in the tissue. In order to plan the dose considering the radiation attenuation, the Convolution algorithm should be used, and additional radiation exposure for computed tomography (CT) and registration errors between MR and CT are entailed. This study investigated the clinical feasibility of synthetic CT (sCT) from GKRS planning MR using deep learning. The model was trained using frame-based contrast-enhanced T1-weighted MR images and corresponding CT slices from 54 training subjects acquired for GKRS planning. The model was applied prospectively to 60 lesions in 43 patients including benign tumor such as meningioma and pituitary adenoma, metastatic brain tumors, and vascular disease of various location for evaluating the model and its application. We evaluated the sCT and compared between treatment plans made with MR only (TMR 10 plan), MR and real CT (rCT; Convolution with rCT [Conv-rCT] plan), and MR and synthetic CT (Convolution with sCT [Conv-sCT] plan). The mean absolute error (MAE) of 43 sCT was 107.35 ± 16.47 Hounsfield units. The TMR 10 treatment plan differed significantly from plans made by Conv-sCT and Conv-rCT. However, the Conv-sCT and Conv-rCT plans were similar. This study showed the practical applicability of deep learning based on sCT in GKRS. Our results support the possibility of formulating GKRS treatment plans while considering radiation attenuation in the tissue using GKRS planning MR and no radiation exposure. © Korean Society of Medical and Biological Engineering 2022.Entities:
Keywords: Artificial intelligence; Deep learning; Gamma Knife radiosurgery; Neuro-oncology; Synthetic CT
Year: 2022 PMID: 36238366 PMCID: PMC9550914 DOI: 10.1007/s13534-022-00227-x
Source DB: PubMed Journal: Biomed Eng Lett ISSN: 2093-9868