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Support Vector Machine Model Predicts Dose for Organs at Risk in High-Dose Rate Brachytherapy of Cervical Cancer

INTRODUCTION: This study aimed to establish a support vector machine (SVM) model to predict the dose for organs at risk (OARs) in intracavitary brachytherapy planning for cervical cancer with tandem and ovoid treatments. METHODS: Fifty patients with loco-regionally advanced cervical cancer treated w...

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Detalles Bibliográficos
Autores principales: Zhou, Ping, Li, Xiaojie, Zhou, Hao, Fu, Xiao, Liu, Bo, Zhang, Yu, Lin, Sheng, Pang, Haowen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319952/
https://www.ncbi.nlm.nih.gov/pubmed/34336640
http://dx.doi.org/10.3389/fonc.2021.619384
Descripción
Sumario:INTRODUCTION: This study aimed to establish a support vector machine (SVM) model to predict the dose for organs at risk (OARs) in intracavitary brachytherapy planning for cervical cancer with tandem and ovoid treatments. METHODS: Fifty patients with loco-regionally advanced cervical cancer treated with 200 CT-based tandem and ovoid brachytherapy plans were included. The brachytherapy plans were randomly divided into the training (N = 160) and verification groups (N = 40). The bladder, rectum, sigmoid colon, and small intestine were divided into sub-OARs. The SVM model was established using MATLAB software based on the sub-OAR volume to predict the bladder, rectum, sigmoid colon, and small intestine [Formula: see text]. Model performance was quantified by mean squared error (MSE) and δ [Formula: see text]. The goodness of fit of the model was quantified by the coefficient of determination (R(2)). The accuracy and validity of the SVM model were verified using the validation group. RESULTS: The [Formula: see text] value of the bladder, rectum, sigmoid colon, and small intestine correlated with the volume of the corresponding sub-OARs in the training group. The mean squared error (MSE) in the SVM model training group was <0.05; the R(2) of each OAR was >0.9. There was no significant difference between the [Formula: see text] -predicted and actual values in the validation group (all P > 0.05): bladder δ = 0.024 ± 0.022, rectum δ = 0.026 ± 0.014, sigmoid colon δ = 0.035 ± 0.023, and small intestine δ = 0.032 ± 0.025. CONCLUSION: The SVM model established in this study can effectively predict the [Formula: see text] for the bladder, rectum, sigmoid colon, and small intestine in cervical cancer brachytherapy.