BioMed Research International

BioMed Research International / 2020 / Article

Research Article | Open Access

Volume 2020 |Article ID 4340521 |

Wenming Li, Dongmin Wei, Aihemaiti Wushouer, Shengda Cao, Tongtong Zhao, Dexin Yu, Dapeng Lei, "Discovery and Validation of a CT-Based Radiomic Signature for Preoperative Prediction of Early Recurrence in Hypopharyngeal Carcinoma", BioMed Research International, vol. 2020, Article ID 4340521, 8 pages, 2020.

Discovery and Validation of a CT-Based Radiomic Signature for Preoperative Prediction of Early Recurrence in Hypopharyngeal Carcinoma

Academic Editor: Ali Gholamrezanezhad
Received02 Mar 2020
Revised28 May 2020
Accepted22 Jun 2020
Published10 Aug 2020


Purpose. In the clinical management of hypopharyngeal squamous cell carcinoma (HSCC), preoperative identification of early recurrence (≤2 years) after curative resection is essential. Thus, we aimed to develop a CT-based radiomic signature to predict early recurrence in HSCC patients preoperatively. Methods. In total, 167 HSCC patients who underwent partial surgery were enrolled in this retrospective study and divided into two groups, i.e., the training cohort () and the validation cohort (). Each individual was followed up for at least for 2 years. Radiomic features were extracted from CT images, and the radiomic signature was built with the least absolute shrinkage and selection operator (LASSO) logistic regression (LR) model. The associations of preoperative clinical factors with early recurrence were evaluated. A radiomic signature-combined model was built, and the area under the curve (AUC) was used to explore their performance in discriminating early recurrence. Results. Among the 1415 features, 335 of them were selected using the variance threshold method. Then, the SelectKBest method was further used for the selection of 31 candidate features. Finally, 11 out of 31 optimal features were identified with the LASSO algorithm. In the LR classifier, the AUCs of the training and validation sets in discriminating early recurrence were 0.83 (95% CI: 0.76-0.90) (sensitivity 0.8 and specificity 0.83) and 0.83 (95% CI: 0.67-0.99) (sensitivity 0.69 and specificity 0.71), respectively. Conclusions. Using the radiomic signature, we developed a radiomic signature to preoperatively predict early recurrence in patients with HSCC, which may serve as a potential noninvasive tool to guide personalized treatment.

1. Introduction

The incidence of hypopharyngeal squamous cell carcinoma (HSCC), one of the common head and neck squamous cell carcinomas, is relatively low among all human cancers. In China and Eastern Europe, the incidence of HSCC is relatively high due to diet habits, tobacco, and alcohol use. In the Western countries, clinicians tend to choose less expensive conservative treatment (radiotherapy and chemotherapy) due to its low incidence [1], while in China, HSCC patients typically receive comprehensive treatment with surgery [2]. A variety of surgical skills and principles have been developed, resulting in significant improvement for laryngeal function and swallowing function [3, 4].

The HSCC are commonly characterized with frequent submucosal spread and early regional lymph node metastasis. A previous clinical analysis revealed that several clinical characteristics might affect the prognosis of HSCC patients, and these characteristics include smoking, drinking, tumor size, T stage, lymph node metastasis, and resection margin [5]. Some molecular markers were found in head and neck tumors, but these markers still did not achieve a relatively high specificity and sensitivity. Thus, it is necessary to further explore other prognostic markers for better individualized treatment. The prognosis of patients with early postoperative recurrence is poor [6]. However, currently, HSCC has few prognostic markers, and the need for improved therapy for better survival of HSCC remains urgent.

With the advance in imaging techniques, the deep data mining is emerging as a new tool in the field of radiology. It may provide the clinicians with more image feature information than the traditional two-dimensional imaging model. The latest technology used for medical imaging might capture the phenotype of tumors noninvasively [7]. The most widely used imaging method is computed tomography (CT), which can quantify tissue density [8]. Recently, increasing attention is paid to using noninvasive methods rather than complex detection in clinical treatment. Medical imaging is a noninvasive, simple, and easy clinical examination technology. Clinicians can determine the tumor’s progress, metastasis, and location of the focus by evaluating the image [9]. Radiology is a mathematical description of image content that can compensate for some measures that lack strict and accurate standards [10]. Although the image texture analysis from conventional imaging techniques such as CT, MRI, and PET remains in the early stage, it has achieved favorable outcomes in the diagnosis and evaluation, as well as prediction in various types of cancer [11]. Texture analysis maximizes image information and has been used in clinical treatment. After optimizing the methods and standardizing the process of radiomics, radiomics may act as a high-potential clinical tool for tumor diagnosis and treatment. However, the role of radiomics in predicting postoperative recurrence in HSCC patients has not been further explored yet.

In this study, based on the CT imaging data in HSCC patients, the CT-based radiomics was employed to develop a novel model for prediction of early recurrence of HSCC in both training and validation datasets. Then, the significant imaging features were selected to generate the prediction model, for which the specificity and sensitivity were determined based on the receiver operating characteristic (ROC) curve analysis. The current study was aimed at providing a new CT-based approach for the preoperative prediction of early recurrence in HSCC patients and at achieving better individualized treatment for improved survival.

2. Material and Methods

2.1. Patients’ Characteristics

The patients were pathologically diagnosed with HSCC. None of the patients underwent preoperative radiotherapy or chemotherapy. The patients had a completely enhanced CT examination in the imaging department of our hospital two weeks before the operation. A total of 167 patients were included in this study between July 2014 and July 2017. After treatment, they were followed up every 3-6 months for electronic laryngoscopy and a neck-enhanced CT examination. The primary endpoint of this study was tumor recurrence. Recurrence was defined as the recurrence of HSCC revealed by CT or laryngoscopy. We used RadCloud (Huiying Medical Technology Co., Ltd.) to manage the imaging data, clinical data, and subsequent radiomic analysis. The training and validation datasets were separated by a random method at a ratio of 8 : 2 (133 cases in the training cohort and 34 cases in the validation cohort). And the number of random seeds was 278. This study was approved by the ethics committee of the Qilu Hospital of Shandong University.

2.2. CT Image Acquisition

All the patients received preoperative enhanced CT scans with multidetector row CT scanners (Discovery CT750HD, GE Healthcare). The scanning parameters were as follows: patient position, supine; scanning range, from the top of the nasopharynx to the entrance of the thorax; slice thickness (5 mm); reconstructed section thickness (0.625 mm); tube voltage (120 kV); tube current (250-400 mA) using automatic tube current modulation; and matrix (). The patients were injected with 1.5 mL/kg of nonionic contrast material (iopromide, Ultravist 300; Bayer) at a rate of 3.0 mL/s via the antecubital vein through a power injector.

2.3. Image Segmentation

In the cloud computing system, the volumes of interest (VOIs) of each patient were delineated manually by two independent senior radiologists. Then, the maximum cross-sectional area of delineated VOIs of the same patient was calculated and compared automatically by the system. If the discrepancy of the mentioned area was ≥5%, another radiologist was involved to delineate the VOI again, in order to reduce the discrepancy to below 5% [12]. Ultimately, 167 VOIs were segmented from 167 patient scans for subsequent analysis.

2.4. Feature Extraction

A total of 1415 quantitative imaging features were extracted from the CT images with the RadCloud platform ( These features were grouped into three groups. Group 1 (first-order statistics) consisted of 126 descriptors that quantitatively delineated the distribution of voxel intensities within the CT image through commonly used and basic metrics; group 2 (shape- and size-based features) contained 14 three-dimensional features that reflected the shape and size of the region; and group 3 (texture features) consisted of 525 textural features that could quantify heterogeneity differences between regions. These features were calculated from gray level run length and gray level cooccurrence texture matrices [13].

2.5. Feature Qualification

A large number of imaging features were computed as described above. All these extracted features were not useful for a particular task. Therefore, dimensionality reduction and the selection of task-specific features were necessary to achieve optimal performance. To reduce the redundant features, feature selection methods, including the variance threshold (), SelectKBest, and the least absolute shrinkage and selection operator (LASSO) [14], were used. For the variance threshold method, the threshold was selected at 0.8; therefore, features with eigenvalues of variance less than 0.8 were removed. The SelectKBest method, a single variable feature selection method, used the value to analyze the relationships between the features and the classification results, and all the features with a value < 0.05 were used. For the LASSO model, L1 regularization was used as the cost function, the error value of crossvalidation was 5, and the maximum number of iterations was 1000.

2.6. Statistical Analysis

After feature qualification, a total of 335 features were significantly correlated to this subject. Based on the selected features, there were several supervised learning classifiers available for classification analysis that created models to separate or predict the data with respect to an outcome or phenotype (e.g., patient outcome or response). In this study, the radiomic-based models were constructed with logistic regression (LR), and the validation method was used to improve the effectiveness of the model. To assess the predictive performance of the model, the area under the curve (AUC) of the receiver operating characteristic (ROC) curve was used in both the training and validation datasets. Four indicators, P (), R (), F1 score (), and support (total number in test set), were used to evaluate the performance of the classifier in this study. All the statistical analyses were performed in the RadCloud platform. Figure 1 depicts the process in the radiomic workflow.

3. Results

The demographic and clinical characteristics of the patients in the training and the validation set are summarized in Supplementary Table 1 (Tab.S1). The Kaplan-Meier method was used for depicting the 5-year overall survival of the group of patients who relapsed within 24 months or not. The log rank test further demonstrated that significantly impaired survival was identified in the early recurrence group in contrast to the nonearly recurrence group as shown in Figure 2(a) (). Figure 2(b) shows the postoperative 5-year overall survival of patients in the training and the validation set, and the difference in overall survival was not significant (). A total of 335 among 1415 features were first selected using the variance threshold method. After using the SelectKBest method, the 31 most significant features were identified (Fig. S1). The final 11 optimal features were selected (Table 1) with the LASSO algorithm (Fig. S2).

Radiomic featureRadiomic classFilter

Long run high gray level emphasisGLRLMWavelet-HHH
Long run low gray level emphasisGLRLMWavelet-LHL
Long run emphasisGLRLMWavelet-HHH
Large dependence high gray level emphasisGLDMWavelet-HHH
MinimumFirst orderWavelet-LLL
SkewnessFirst orderWavelet-HLH
Total energyFirst orderSquare
Zone entropyGLSZMWavelet-LHL
Dependence varianceGLDMWavelet-LLH
Total energyFirst orderExponential
Long run high gray level emphasisGLRLMWavelet-LHH

Labels: GLDM: gray level dependence matrix; GLRLM: gray level run length matrix; GLSZM: gray level size zone matrix.

The ROC curve analyses in the training and validation sets are shown in Table 2. When training with the LR classifier, the AUC of the training set in discriminating early recurrence was 0.83 (95% CI: 0.76-0.90) with a sensitivity of 0.80 and specificity of 0.83, and the AUC of the validation set was 0.83 (95% CI: 0.67-0.99) with a sensitivity of 0.69 and specificity of 0.71 (Figure 3).We summarize these four indicators (i.e., precision, recall, F1 score, and support) for classifiers in Table 3. When training with the LR classifier, the precision, recall, F1 score, and support of the training set in discriminating early recurrence were 0.87, 0.83, 0.85, and 83, respectively, and those of the validation set were 0.79, 0.71, 0.75, and 21, respectively.

ClassifierCategoryAUC95% CISensitivitySpecificity



F1 score0.85

F1 score0.75

The recurrent risk ratio of each individual could be obtained from the RadCloud platform based on their own 11 selected radiomic signatures. Then, the cases in the training and validation cohorts were, respectively, classified into two groups, i.e., the high-risk group (with ) and the low-risk group (with ). As shown in Figure 4(a), in the training cohort, the 5-year overall survival in the high-risk group was significantly reduced than that in the low-risk group (). The similar results were observed in the validation cohort (Figure 4(b), ). Taken together, these data supported the reproducibility of the developed model in the prediction of recurrence in this study.

4. Discussion

Radiomic features, such as intensity and shape, provide amounts of information on tumor phenotypes [15]. Radiomics are recognized as a promising tool to improve predictive accuracy of the diagnosis and prognosis through quantifying phenotypic characteristics on medical imaging and the use of automated algorithms [16, 17]. A growing number of radiomic nanograms have been developed for preoperative prediction of lymph node (LN) metastasis, response to neoadjuvant chemoradiotherapy, and recurrence in malignancies [1820]. In this study, we assessed the role of CT-based radiomics in preoperative prediction of recurrence of HSCC.

In total, 1415 radiomic features were extracted for CT images of each patient. Then, the LASSO Cox regression model and SelectKBest method were applied, leading to identification of the 11 most significant features. Further, the sensitivity and specificity of the predictive model dependent on the 11 features were assessed by calculating the AUC, suggesting that CT-based radiomic features could sensitively recognize individuals who were vulnerable to relapse. Our survival analysis demonstrated that patients with a high risk of recurrence as estimated by the model had worse prognoses than those with low risk, suggesting the clinical value of our established predictive model. Likewise, the predictive role of CT radiomic signature was also evaluated in other types of malignancies, such as hepatocellular carcinoma [21, 22], gastric cancer [23], and non-small cell lung cancer [24]. Apart from that, CT-based radiomics have also been proven as prognostic biomarkers in breast cancer [25] and hepatocellular carcinoma [26] as well as HNSCC. Taken together, we tentatively believe that the CT-based radiomic signature is emerging as a promising noninvasive approach to evaluation of patients with malignancy, including HSCC. There is a debate on which imaging tool has superior performance in terms of radiomics, CT or MRI. MRI is superior to CT in better soft tissue contrast and imaging quality, while CT can provide finer spatial resolution and less obvious artifacts caused by motion during scanning [27]. For HSCC, motion artifact is less evident than other parts of the body, such as the chest. And it has been reported that MRI can potentially serve as the prognostic biomarker for HNSCC patients [28, 29], mainly nasopharyngeal carcinoma and oral cavity and oropharyngeal squamous cell carcinomas. Thus, we think that MRI may be an alternative modality used for predicting recurrence of HSCC in our further study.

Liao et al. performed radiomic feature analysis of positron emission tomography (PET) images in a cohort of 80 oropharyngeal and hypopharyngeal cancer patients and found that PET images might predict recurrence of these cancers [30]. The PET-based radiomics showed a benefit in preoperatively predicting recurrence, with a similar AUC value to that in our study. However, a significant advantage of CT over PET in cost makes CT a more promising modality than PET in the radiomic-based recurrence prediction of HSCC. Our study appeared more convincing because our study had a relatively larger sample size (167 HSCC cases) than that in the study by Liao et al. (40 cases). Mo et al. also developed a CT radiomic-based model, showing a well discriminative performance in stratifying the risk of early progression (recurrence or metastasis) among113 patients with HSCC [31]. Compared to our models, they developed models including both radiomic and clinical variables, making it more comprehensive and clinically rational. Their model was applied in HSCC patients with chemoradiotherapy, while our model was developed in HSCC patients with surgery and postoperative radiotherapy.

Our research has several limitations. Firstly, because it is a retrospective study from a single hospital, the selection bias exists. Secondly, we selected the CT image data only in this imaging analysis; it is difficult to comprehensively evaluate the estimation without other imaging data. Additionally, it is one-sided to analyze radiomic features from the largest cross-sectional area of the tumor rather than the whole tumor. Thirdly, the sample sizes are relatively small, while a larger prospective cohort is needed to validate our findings from the current study.

In conclusion, we primarily identified the predictive role of CT-based radiomics in the preoperative prediction of early recurrence of patients with HSCC, and our radiomic signature may have potential as a noninvasive tool for the pretreatment evaluation of patients with HSCC. However, a future well-designed, larger prospective study is needed to validate our findings.


CT:Computed tomography
HSCC:Hypopharyngeal squamous cell carcinoma
LASSO:Least absolute shrinkage and selection operator
LR:Logistic regression
AUC:Area under the curve.

Data Availability

The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions.

Conflicts of Interest

The authors declare that they have no conflicts of interest.


This work was supported by the new technology development fund for clinical application of the Qilu Hospital of Shandong University, Jinan, Shandong, China [grant numbers 2018-2 and 2019-16].

Supplementary Materials

Table S1: clinical characteristics of the patients. Figure S1: SelectKBest method was used for preliminarily selecting radiomic features potentially associated with early recurrence of HSCC using data of the training cohort. Figure S2: LASSO algorithm for feature selection. (a) LASSO path, (b) MSE path, and (c) coefficients in the LASSO model. Eleven features that correspond to the optimal alpha value were selected in the LASSO model. (Supplementary Materials)


  1. K. D. Shield, J. Ferlay, A. Jemal et al., “The global incidence of lip, oral cavity, and pharyngeal cancers by subsite in 2012,” CA: a Cancer Journal for Clinicians, vol. 67, no. 1, pp. 51–64, 2017. View at: Publisher Site | Google Scholar
  2. T. Jin, X. Li, D. Lei et al., “Preservation of laryngeal function improves outcomes of patients with hypopharyngeal carcinoma,” European Archives of Oto-Rhino-Laryngology, vol. 272, no. 7, pp. 1785–1791, 2015. View at: Publisher Site | Google Scholar
  3. A. Bozec, D. Culié, G. Poissonnet, and O. Dassonville, “Current role of primary surgical treatment in patients with head and neck squamous cell carcinoma,” Current Opinion in Oncology, vol. 31, no. 3, pp. 138–145, 2019. View at: Publisher Site | Google Scholar
  4. C.-T. Cheng, C. Y. Lin, S. Hung-Chun Cheng et al., “Survival benefit of surgical approach for advanced oropharyngeal and hypopharyngeal cancer: a retrospective analysis,” Head & Neck, vol. 39, no. 10, pp. 2104–2113, 2017. View at: Publisher Site | Google Scholar
  5. A. Eskander, M. Mifsud, J. Irish et al., “Overview of surgery for laryngeal and hypopharyngeal cancer in Ontario, 2003-2010,” Head & Neck, vol. 39, no. 8, pp. 1559–1567, 2017. View at: Publisher Site | Google Scholar
  6. R. B. Smith, “Surgery in the management of laryngeal and hypopharyngeal carcinoma,” International Journal of Radiation Oncology • Biology • Physics, vol. 69, no. 2, pp. S28–S30, 2007. View at: Publisher Site | Google Scholar
  7. K. M. Panth, R. T. H. Leijenaar, S. Carvalho et al., “Is there a causal relationship between genetic changes and radiomics-based image features? An in vivo preclinical experiment with doxycycline inducible GADD34 tumor cells,” Radiotherapy and Oncology, vol. 116, no. 3, pp. 462–466, 2015. View at: Publisher Site | Google Scholar
  8. C. Parmar, R. T. H. Leijenaar, P. Grossmann et al., “Radiomic feature clusters and prognostic signatures specific for lung and head & neck cancer,” Scientific Reports, vol. 5, no. 1, article 11044, 2015. View at: Publisher Site | Google Scholar
  9. C. M. Chiesa-Estomba, O. Echaniz, E. Larruscain, J. A. Gonzalez-Garcia, J. A. Sistiaga-Suarez, and M. Graña, “Radiomics and texture analysis in laryngeal cancer. Looking for new frontiers in precision medicine through imaging analysis,” Cancers, vol. 11, no. 10, article 1409, 2019. View at: Publisher Site | Google Scholar
  10. R. L. Hesketh, A. X. Zhu, and R. Oklu, “Radiomics and circulating tumor cells: personalized care in hepatocellular carcinoma,” Diagnostic and Interventional Radiology, vol. 21, no. 1, pp. 78–84, 2015. View at: Publisher Site | Google Scholar
  11. H. Peng, D. Dong, M. J. Fang et al., “Prognostic value of deep learning PET/CT-based radiomics: potential role for future individual induction chemotherapy in advanced nasopharyngeal carcinoma,” Clinical Cancer Research, vol. 25, no. 14, pp. 4271–4279, 2019. View at: Publisher Site | Google Scholar
  12. P. Lambin, E. Rios-Velazquez, R. Leijenaar et al., “Radiomics: extracting more information from medical images using advanced feature analysis,” European Journal of Cancer, vol. 48, no. 4, pp. 441–446, 2012. View at: Publisher Site | Google Scholar
  13. V. Kumar, Y. Gu, S. Basu et al., “Radiomics: the process and the challenges,” Magnetic Resonance Imaging, vol. 30, no. 9, pp. 1234–1248, 2012. View at: Publisher Site | Google Scholar
  14. B. Zhang, J. Tian, D. Dong et al., “Radiomics features of multiparametric MRI as novel prognostic factors in advanced nasopharyngeal carcinoma,” Clinical Cancer Research, vol. 23, no. 15, pp. 4259–4269, 2017. View at: Publisher Site | Google Scholar
  15. P. Lambin, R. T. H. Leijenaar, T. M. Deist et al., “Radiomics: the bridge between medical imaging and personalized medicine,” Nature Reviews Clinical Oncology, vol. 14, no. 12, pp. 749–762, 2017. View at: Publisher Site | Google Scholar
  16. J. J. M. van Griethuysen, A. Fedorov, C. Parmar et al., “Computational radiomics system to decode the radiographic phenotype,” Cancer Research, vol. 77, no. 21, pp. e104–e107, 2017. View at: Publisher Site | Google Scholar
  17. Z. Liu, S. Wang, D. Dong et al., “The applications of radiomics in precision diagnosis and treatment of oncology: opportunities and challenges,” Theranostics, vol. 9, no. 5, pp. 1303–1322, 2019. View at: Publisher Site | Google Scholar
  18. Y. Q. Huang, C. H. Liang, L. He et al., “Development and validation of a radiomics nomogram for preoperative prediction of lymph node metastasis in colorectal cancer,” Journal of Clinical Oncology, vol. 34, no. 18, pp. 2157–2164, 2016. View at: Publisher Site | Google Scholar
  19. Z. Liu, X. Y. Zhang, Y. J. Shi et al., “Radiomics analysis for evaluation of pathological complete response to neoadjuvant chemoradiotherapy in locally advanced rectal cancer,” Clinical Cancer Research, vol. 23, no. 23, pp. 7253–7262, 2017. View at: Publisher Site | Google Scholar
  20. H. Park, Y. Lim, E. S. Ko et al., “Radiomics signature on magnetic resonance imaging: association with disease-free survival in patients with invasive breast cancer,” Clinical Cancer Research, vol. 24, no. 19, pp. 4705–4714, 2018. View at: Publisher Site | Google Scholar
  21. Y. Zhou, L. He, Y. Huang et al., “CT-based radiomics signature: a potential biomarker for preoperative prediction of early recurrence in hepatocellular carcinoma,” Abdominal Radiology, vol. 42, no. 6, pp. 1695–1704, 2017. View at: Publisher Site | Google Scholar
  22. Q. Y. Shan, H. T. Hu, S. T. Feng et al., “CT-based peritumoral radiomics signatures to predict early recurrence in hepatocellular carcinoma after curative tumor resection or ablation,” Cancer Imaging, vol. 19, no. 1, p. 11, 2019. View at: Publisher Site | Google Scholar
  23. W. Zhang, M. Fang, D. Dong et al., “Development and validation of a CT-based radiomic nomogram for preoperative prediction of early recurrence in advanced gastric cancer,” Radiotherapy and Oncology, vol. 145, pp. 13–20, 2020. View at: Publisher Site | Google Scholar
  24. Q. Li, J. Kim, Y. Balagurunathan et al., “CT imaging features associated with recurrence in non-small cell lung cancer patients after stereotactic body radiotherapy,” Radiation Oncology, vol. 12, no. 1, p. 158, 2017. View at: Publisher Site | Google Scholar
  25. O. Weaver and J. W. T. Leung, “Biomarkers and imaging of breast cancer,” American Journal of Roentgenology, vol. 210, no. 2, pp. 271–278, 2018. View at: Publisher Site | Google Scholar
  26. L. Cozzi, N. Dinapoli, A. Fogliata et al., “Radiomics based analysis to predict local control and survival in hepatocellular carcinoma patients treated with volumetric modulated arc therapy,” BMC Cancer, vol. 17, no. 1, p. 829, 2017. View at: Publisher Site | Google Scholar
  27. D. W. Tshering Vogel and H. C. Thoeny, “Cross-sectional imaging in cancers of the head and neck: how we review and report,” Cancer Imaging, vol. 16, no. 1, p. 20, 2016. View at: Publisher Site | Google Scholar
  28. Y. Yuan, J. Ren, Y. Shi, and X. Tao, “MRI-based radiomic signature as predictive marker for patients with head and neck squamous cell carcinoma,” European Journal of Radiology, vol. 117, pp. 193–198, 2019. View at: Publisher Site | Google Scholar
  29. L. Zhang, H. Zhou, D. Gu et al., “Radiomic nomogram: pretreatment evaluation of local recurrence in nasopharyngeal carcinoma based on MR imaging,” Journal of Cancer, vol. 10, no. 18, pp. 4217–4225, 2019. View at: Publisher Site | Google Scholar
  30. K. Y.-K. Liao, C.-C. Chiu, W.-C. Chiang et al., “Radiomics features analysis of PET images in oropharyngeal and hypopharyngeal cancer,” Medicine, vol. 98, no. 18, article e15446, 2019. View at: Publisher Site | Google Scholar
  31. X. Mo, X. Wu, D. Dong et al., “Prognostic value of the radiomics-based model in progression-free survival of hypopharyngeal cancer treated with chemoradiation,” European Radiology, vol. 30, no. 2, pp. 833–843, 2020. View at: Publisher Site | Google Scholar

Copyright © 2020 Wenming Li et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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