TY - GEN
T1 - MR-radiomic biopsy for estimation of malignancy grade in parotid gland cancer
AU - Kamezawa, H.
AU - Arimura, H.
AU - Yasumatsu, R.
AU - Ninomiya, K.
N1 - Funding Information:
This research was supported by JSPS KAKENHI Grant Number JP 17K15808. The authors express their gratitude to all members of the Arimura Laboratory (http://www.shs.kyushu-u.ac.jp/~arimura) for valuable comments and helpful discussions.
Publisher Copyright:
© COPYRIGHT SPIE. Downloading of the abstract is permitted for personal use only.
PY - 2020
Y1 - 2020
N2 - We have developed a magnetic resonance (MR) image-based radiomic biopsy approach for estimation of malignancy grade in parotid gland cancer (PGC). Preoperative T1- and T2-weighted MR images of 39 PGC patients with 20 highand 19 intermediate-/low-malignancy grades were employed. High- versus intermediate-/low-malignancy grades were estimated using MR-radiomic biopsy approaches, i.e. 972 hand-crafted feature and transfer learning of five pre-trained deep learning (DL) architectures (AlexNet, GoogLeNet, VGG-16, ResNet-101, DenseNet-201). The 39 patients were divided into 70% for training datasets and 30% for test datasets. The hand-crafted features were extracted from cancer regions in T1- and T2-weighted MR images. Three features were selected as a radiomic signature by using a least absolute shrinkage and selection operator (LASSO), whose coefficients of three features were used for constructing the radiomic score (Rad-score). The two grade malignancy was estimated by using an optimal cut-off value of Rad-score. On the other hand, last three layers of the DL architectures were replaced with new three layers for the estimation task. The DL architectures were fine-tuned with training datasets and were evaluated with test datasets. The performances of the MR-radiomic biopsy approaches were assessed by using the accuracy and the area under the receiver operating characteristic curve (AUC). The VGG-16 demonstrated the best performance (accuracy=85.4%, AUC=0.906), but the other approaches showed worse performances (Rad-score: 83.3%, 0.830, AlexNet: 84.4%, 0.915, GoogLeNet: 84.9%, 0.884, ResNet-101: 84.9%, 0.918, DenseNet-201: 84.4%, 0.869) than the VGG-16. The VGG-16-based MR-radiomic biopsy could be feasible for the malignancy grade estimation of PGC.
AB - We have developed a magnetic resonance (MR) image-based radiomic biopsy approach for estimation of malignancy grade in parotid gland cancer (PGC). Preoperative T1- and T2-weighted MR images of 39 PGC patients with 20 highand 19 intermediate-/low-malignancy grades were employed. High- versus intermediate-/low-malignancy grades were estimated using MR-radiomic biopsy approaches, i.e. 972 hand-crafted feature and transfer learning of five pre-trained deep learning (DL) architectures (AlexNet, GoogLeNet, VGG-16, ResNet-101, DenseNet-201). The 39 patients were divided into 70% for training datasets and 30% for test datasets. The hand-crafted features were extracted from cancer regions in T1- and T2-weighted MR images. Three features were selected as a radiomic signature by using a least absolute shrinkage and selection operator (LASSO), whose coefficients of three features were used for constructing the radiomic score (Rad-score). The two grade malignancy was estimated by using an optimal cut-off value of Rad-score. On the other hand, last three layers of the DL architectures were replaced with new three layers for the estimation task. The DL architectures were fine-tuned with training datasets and were evaluated with test datasets. The performances of the MR-radiomic biopsy approaches were assessed by using the accuracy and the area under the receiver operating characteristic curve (AUC). The VGG-16 demonstrated the best performance (accuracy=85.4%, AUC=0.906), but the other approaches showed worse performances (Rad-score: 83.3%, 0.830, AlexNet: 84.4%, 0.915, GoogLeNet: 84.9%, 0.884, ResNet-101: 84.9%, 0.918, DenseNet-201: 84.4%, 0.869) than the VGG-16. The VGG-16-based MR-radiomic biopsy could be feasible for the malignancy grade estimation of PGC.
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U2 - 10.1117/12.2549462
DO - 10.1117/12.2549462
M3 - Conference contribution
AN - SCOPUS:85082578949
T3 - Progress in Biomedical Optics and Imaging - Proceedings of SPIE
BT - Medical Imaging 2020
A2 - Chen, Po-Hao
A2 - Deserno, Thomas M.
PB - SPIE
T2 - Medical Imaging 2020: Imaging Informatics for Healthcare, Research, and Applications
Y2 - 16 February 2020 through 17 February 2020
ER -