Deep learning based automatic internal gross target volume delineation from 4D-CT of hepatocellular carcinoma patients

被引:2
|
作者
Yang, Zhen [1 ]
Yang, Xiaoyu [1 ]
Cao, Ying [1 ]
Shao, Qigang [1 ]
Tang, Du [1 ]
Peng, Zhao [1 ]
Di, Shuanhu [2 ]
Zhao, Yuqian [2 ]
Li, Shuzhou [1 ,3 ]
机构
[1] Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Dept Oncol, Changsha, Peoples R China
[2] Cent South Univ, Sch Automat, Changsha, Peoples R China
[3] Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Dept Oncol, Changsha 410008, Hunan, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
4D-CT; automated delineation; deep learning; hepatocellular carcinoma; internal gross target volume; STEREOTACTIC BODY RADIOTHERAPY; CONFORMAL RADIATION-THERAPY; INDUCED LIVER-DISEASE;
D O I
10.1002/acm2.14211
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
BackgroundThe location and morphology of the liver are significantly affected by respiratory motion. Therefore, delineating the gross target volume (GTV) based on 4D medical images is more accurate than regular 3D-CT with contrast. However, the 4D method is also more time-consuming and laborious. This study proposes a deep learning (DL) framework based on 4D-CT that can achieve automatic delineation of internal GTV.MethodsThe proposed network consists of two encoding paths, one for feature extraction of adjacent slices (spatial slices) in a specific 3D-CT sequence, and one for feature extraction of slices at the same location in three adjacent phase 3D-CT sequences (temporal slices), a feature fusion module based on an attention mechanism was proposed for fusing the temporal and spatial features. Twenty-six patients' 4D-CT, each consisting of 10 respiratory phases, were used as the dataset. The Hausdorff distance (HD95), Dice similarity coefficient (DSC), and volume difference (VD) between the manual and predicted tumor contour were computed to evaluate the model's segmentation accuracy.ResultsThe predicted GTVs and IGTVs were compared quantitatively and visually with the ground truth. For the test dataset, the proposed method achieved a mean DSC of 0.869 +/- 0.089 and an HD95 of 5.14 +/- 3.34 mm for all GTVs, with under-segmented GTVs on some CT slices being compensated by GTVs on other slices, resulting in better agreement between the predicted IGTVs and the ground truth, with a mean DSC of 0.882 +/- 0.085 and an HD95 of 4.88 +/- 2.84 mm. The best GTV results were generally observed at the end-inspiration stage.ConclusionsOur proposed DL framework for tumor segmentation on 4D-CT datasets shows promise for fully automated delineation in the future. The promising results of this work provide impetus for its integration into the 4DCT treatment planning workflow to improve hepatocellular carcinoma radiotherapy.
引用
收藏
页数:12
相关论文
共 50 条
  • [21] A Survey on Automatic Delineation of Radiotherapy Target Volume based on Machine Learning
    Tao, Zhenchao
    Lyu, Shengfei
    DATA INTELLIGENCE, 2023, 5 (03) : 841 - 856
  • [22] Inter-observer and intra-observer reliability for lung cancer target volume delineation in the 4D-CT era
    Louie, Alexander V.
    Rodrigues, George
    Olsthoorn, Jason
    Palma, David
    Yu, Edward
    Yaremko, Brian
    Ahmad, Bela
    Aivas, Inge
    Gaede, Stewart
    RADIOTHERAPY AND ONCOLOGY, 2010, 95 (02) : 166 - 171
  • [23] Inter-observer and intra-observer reliability for lung cancer target volume delineation in the 4D-CT era
    Rodrigues, George
    Louie, Alexander
    Olsthoorn, Jason
    Palma, David
    Yu, Edward
    Yaremko, Brian
    Ahmad, Belal
    Aivas, Inge
    Gaede, Stewart
    JOURNAL OF THORACIC ONCOLOGY, 2009, 4 (09) : S532 - S533
  • [24] To Study the Feasibility and Potential Benefit of Defining the Internal Gross Tumor Volume (ITV) for Hepatocellular Carcinoma (HCC) Applying the Contrast-Enhanced 4D-CT Obtained by Deformable Registration Technology
    Gong, G.
    Hua, X.
    Yong, Y.
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2014, 90 : S837 - S838
  • [25] Inter-observer and Intra-observer Reliability for Lung Cancer Target Volume Delineation in the 4D-CT Era
    Louie, A. V.
    Rodrigues, G.
    Olsthoorn, J.
    Palma, D.
    Yu, E.
    Yaremko, B.
    Ahmad, B.
    Aivas, I.
    Gaede, S.
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2009, 75 (03): : S472 - S473
  • [26] Comparison of CT and integrated PET-CT-based gross tumor volume delineation for radiotherapy in patients with pancreatic carcinoma
    Liu, N.
    Yuan, Z.
    Xu, Y.
    Zhu, L.
    Zhang, Bailin
    You, Jinqiang
    Sun, Jian
    Yang, Chengwen
    Zhao, Lujun
    JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (15)
  • [27] Semiautomatic technique for defining the internal gross tumor volume of lung tumors close to liver/spleen cupola by 4D-CT
    Mancosu, Pietro
    Sghedoni, Roberto
    Bettinardi, Valentino
    Aquilina, Mark Anthony
    Navarria, Piera
    Cattaneo, Giovanni Mauro
    Di Muzio, Nadia
    Cozzi, Luca
    Scorsetti, Marta
    MEDICAL PHYSICS, 2010, 37 (09) : 4572 - 4576
  • [28] An evaluation of an automated 4D-CT contour propagation tool to define an internal gross tumour volume for lung cancer radiotherapy
    Gaede, Stewart
    Olsthoorn, Jason
    Louie, Alexander V.
    Palma, David
    Yu, Edward
    Yaremko, Brian
    Ahmad, Belal
    Chen, Jeff
    Bzdusek, Karl
    Rodrigues, George
    RADIOTHERAPY AND ONCOLOGY, 2011, 101 (02) : 322 - 328
  • [29] Advances in gross tumor target volume determination in radiotherapy for patients with hepatocellular carcinoma
    Meng, Kangning
    Gong, Guanzhong
    Liu, Rui
    Du, Shanshan
    Yin, Yong
    FRONTIERS IN ONCOLOGY, 2024, 14
  • [30] Automated delineation of nasopharynx gross tumor volume for nasopharyngeal carcinoma by plain CT combining contrast-enhanced CT using deep learning
    Wang, Xuetao
    Yang, Geng
    Zhang, Yiwen
    Zhu, Lin
    Xue, Xiaoguang
    Zhang, Bailin
    Cai, Chunya
    Jin, Huaizhi
    Zheng, Jianxiao
    Wu, Jian
    Yang, Wei
    Dai, Zhenhui
    JOURNAL OF RADIATION RESEARCH AND APPLIED SCIENCES, 2020, 13 (01) : 568 - 577