TY - JOUR
T1 - Multi-Organ Omics-Based Prediction for Adaptive Radiation Therapy Eligibility in Nasopharyngeal Carcinoma Patients Undergoing Concurrent Chemoradiotherapy
AU - Lam, Sai Kit
AU - Zhang, Yuanpeng
AU - Zhang, Jiang
AU - Li, Bing
AU - Sun, Jia Chen
AU - Liu, Carol Yee Tung
AU - Chou, Pak Hei
AU - Teng, Xinzhi
AU - Ma, Zong Rui
AU - Ni, Rui Yan
AU - Zhou, Ta
AU - Peng, Tao
AU - Xiao, Hao Nan
AU - Li, Tian
AU - Ren, Ge
AU - Cheung, Andy Lai Yin
AU - Lee, Francis Kar Ho
AU - Yip, Celia Wai Yi
AU - Au, Kwok Hung
AU - Lee, Victor Ho Fun
AU - Chang, Amy Tien Yee
AU - Chan, Lawrence Wing Chi
AU - Cai, Jing
N1 - Funding Information:
This research was partly supported by research grants of Innovation and Technology Fund (ITS/080/19), the Innovation and Technology Commission, and Project of Strategic Importance Fund (P0035421), The Hong Kong Polytechnic University, The Government of the Hong Kong Special Administrative Region.
Publisher Copyright:
Copyright © 2022 Lam, Zhang, Zhang, Li, Sun, Liu, Chou, Teng, Ma, Ni, Zhou, Peng, Xiao, Li, Ren, Cheung, Lee, Yip, Au, Lee, Chang, Chan and Cai.
PY - 2022/1/31
Y1 - 2022/1/31
N2 - Purpose: To investigate the role of different multi-organ omics-based prediction models for pre-treatment prediction of Adaptive Radiotherapy (ART) eligibility in patients with nasopharyngeal carcinoma (NPC). Methods and Materials: Pre-treatment contrast-enhanced computed tomographic and magnetic resonance images, radiotherapy dose and contour data of 135 NPC patients treated at Hong Kong Queen Elizabeth Hospital were retrospectively analyzed for extraction of multi-omics features, namely Radiomics (R), Morphology (M), Dosiomics (D), and Contouromics (C), from a total of eight organ structures. During model development, patient cohort was divided into a training set and a hold-out test set in a ratio of 7 to 3 via 20 iterations. Four single-omics models (R, M, D, C) and four multi-omics models (RD, RC, RM, RMDC) were developed on the training data using Ridge and Multi-Kernel Learning (MKL) algorithm, respectively, under 10-fold cross validation, and evaluated on hold-out test data using average area under the receiver-operator-characteristics curve (AUC). The best-performing single-omics model was first determined by comparing the AUC distribution across the 20 iterations among the four single-omics models using two-sided student t-test, which was then retrained using MKL algorithm for a fair comparison with the four multi-omics models. Results: The R model significantly outperformed all other three single-omics models (all p-value<0.0001), achieving an average AUC of 0.942 (95%CI: 0.938-0.946) and 0.918 (95%CI: 0.903-0.933) in training and hold-out test set, respectively. When trained with MKL, the R model (R_MKL) yielded an increased AUC of 0.984 (95%CI: 0.981-0.988) and 0.927 (95%CI: 0.905-0.948) in training and hold-out test set respectively, while demonstrating no significant difference as compared to all studied multi-omics models in the hold-out test sets. Intriguingly, Radiomic features accounted for the majority of the final selected features, ranging from 64% to 94%, in all the studied multi-omics models. Conclusions: Among all the studied models, the Radiomic model was found to play a dominant role for ART eligibility in NPC patients, and Radiomic features accounted for the largest proportion of features in all the multi-omics models.
AB - Purpose: To investigate the role of different multi-organ omics-based prediction models for pre-treatment prediction of Adaptive Radiotherapy (ART) eligibility in patients with nasopharyngeal carcinoma (NPC). Methods and Materials: Pre-treatment contrast-enhanced computed tomographic and magnetic resonance images, radiotherapy dose and contour data of 135 NPC patients treated at Hong Kong Queen Elizabeth Hospital were retrospectively analyzed for extraction of multi-omics features, namely Radiomics (R), Morphology (M), Dosiomics (D), and Contouromics (C), from a total of eight organ structures. During model development, patient cohort was divided into a training set and a hold-out test set in a ratio of 7 to 3 via 20 iterations. Four single-omics models (R, M, D, C) and four multi-omics models (RD, RC, RM, RMDC) were developed on the training data using Ridge and Multi-Kernel Learning (MKL) algorithm, respectively, under 10-fold cross validation, and evaluated on hold-out test data using average area under the receiver-operator-characteristics curve (AUC). The best-performing single-omics model was first determined by comparing the AUC distribution across the 20 iterations among the four single-omics models using two-sided student t-test, which was then retrained using MKL algorithm for a fair comparison with the four multi-omics models. Results: The R model significantly outperformed all other three single-omics models (all p-value<0.0001), achieving an average AUC of 0.942 (95%CI: 0.938-0.946) and 0.918 (95%CI: 0.903-0.933) in training and hold-out test set, respectively. When trained with MKL, the R model (R_MKL) yielded an increased AUC of 0.984 (95%CI: 0.981-0.988) and 0.927 (95%CI: 0.905-0.948) in training and hold-out test set respectively, while demonstrating no significant difference as compared to all studied multi-omics models in the hold-out test sets. Intriguingly, Radiomic features accounted for the majority of the final selected features, ranging from 64% to 94%, in all the studied multi-omics models. Conclusions: Among all the studied models, the Radiomic model was found to play a dominant role for ART eligibility in NPC patients, and Radiomic features accounted for the largest proportion of features in all the multi-omics models.
KW - adaptive radiotherapy
KW - dosiomics
KW - multiomics approach
KW - nasopharyngeal carcinoma
KW - radiomics
UR - http://www.scopus.com/inward/record.url?scp=85124712569&partnerID=8YFLogxK
U2 - 10.3389/fonc.2021.792024
DO - 10.3389/fonc.2021.792024
M3 - Journal article
AN - SCOPUS:85124712569
SN - 2234-943X
VL - 11
JO - Frontiers in Oncology
JF - Frontiers in Oncology
M1 - 792024
ER -