Skip to main content

A CT based radiomics analysis to predict the CN0 status of thyroid papillary carcinoma: a two- center study

Abstract

Objectives

To develop and validate radiomics model based on computed tomography (CT) for preoperative prediction of CN0 status in patients with papillary thyroid carcinoma (PTC).

Methods

A total of 548 pathologically confirmed LNs (243 non-metastatic and 305 metastatic) two distinct hospitals were retrospectively assessed. A total of 396 radiomics features were extracted from arterial-phase CT images, where the strongest features containing the most predictive potential were further selected using the least absolute shrinkage and selection operator (LASSO) regression method. Delong test was used to compare the AUC values of training set, test sets and cN0 group.

Results

The Rad-score showed good discriminating performance with Area Under the ROC Curve (AUC) of 0.917(95% CI, 0.884 to 0.950), 0.892 (95% CI, 0.833 to 0.950) and 0.921 (95% CI, 868 to 0.973) in the training, internal validation cohort and external validation cohort, respectively. The test group of CN0 with a AUC of 0.892 (95% CI, 0.805 to 0.979). The accuracy was 85.4% (sensitivity = 81.3%; specificity = 88.9%) in the training cohort, 82.9% (sensitivity = 79.0%; specificity = 88.7%) in the internal validation cohort, 85.4% (sensitivity = 89.7%; specificity = 83.8%) in the external validation cohort, 86.7% (sensitivity = 83.8%; specificity = 91.3%) in the CN0 test group.The calibration curve demonstrated a significant Rad-score (P-value in H-L test > 0.05). The decision curve analysis indicated that the rad-score was clinically useful.

Conclusions

Radiomics has shown great diagnostic potential to preoperatively predict the status of cN0 in PTC.

Key Points

  • Radiomics has shown great diagnostic potential to preoperatively predict the status of cN0 in PTC.

  • Retrospective two-center study showed that radiomics has provides greater diagnostic confidence.

Introduction

Cervical LN postoperative metastasis has been associated with local recurrence and distant metastasis, negatively affecting patient survival [1,2,3]. Therapeutically, central neck LN dissection (CND) has been recommended for patients with lymph node involvement [4,5,6]. European Thyroid Association (ETA) and the Korean Society of Thyroid Radiology (KSThR) divides lymph nodes into three groups according to US features, including suspicious, indeterminate LNs and benign LNs. We defined indeterminate LNs and benign LNs as clinically node-negative (cN0). For clinically node-negative (cN0) patients, American Thyroid Association (ATA) and Asian guidelines are controversial on whether to perform prophylactic central neck dissection(pCND). However, we found that some lymph nodes diagnosed as cN0 confirmed by ultrasound were pathologically proved as metastatic lymph nodes. The risk of surgical complications such as hypoparathyroidism and recurrent laryngeal nerve injury may occur after performing pCND [3, 7,8,9,10]. There may be a risk of postoperative recurrence without pCND [11]. Whether to implement preventive central neck dissection (pCND) depends on the authenticity of cN0. Therefore, we need to find a way to improve the authenticity of cN0 state detection. As a non-invasive examination, imaging is an effective alternative examination method.

Traditional imaging plays a key role in the preoperative assessment of cervical LN metastasis for PTC patients. Preoperative neck ultrasound (US) for cervical LNs has been recommended for all patients undergoing thyroidectomy [2, 4,5,6]. In a meta-analysis, CT demonstrated a higher sensitivity of 62% than US (51%) and there was no difference in specificity in detecting LN metastasis, but the performance was still unsatisfactory [8, 12]. In summary, the limited sensitivity of traditional imaging for cervical LN metastasis may cause many patients to be misdiagnosed as cN0.

Radiomics is a method that extracts large amount of features from radiographic medical images using algorithms of data characterization, and made some positive result in preoperative evaluation of LN metastasis of variety of cancers [13,14,15,16,17,18]. Up to now, there is no relevant study about preoperatively predicting the authenticity of cN0 status by radiomics model based on CT images.

Therefore, the purpose of this study is to establish a radiomics model based on arterial CT images of LNs to predict LN status and explore if the model can be used for detecting cervical LN metastasis of clinical LN negative (cN0) patients in PTC.

Materials and methods

Patients/lymph node

Ethics license was received from the Science Ethics Committee. This study is a retrospective study and informed consents were waived. This work complied with the Declaration of Helsinki.

Patients were selected from a cohort who was consecutively treated in two independent centers. The study was conducted between January 2015 and February 2019 in Center #1, and from December 2016 to December 2019 in Center #2.

Inclusion criteria

Patients: a)patients who were diagnosed with PTC by paraffin-based pathologic examination and underwent enhanced CT examination before preoperative within one month; b)the number of central neck lymph nodes dissected were ≥ 4;

Lymph node: (a) all dissected central neck LNs were confirmed (i.e. metastasis/no metastasis) by paraffin-based pathologic examination; (b) the short diameter of the lymph node (for each selected LN) should be greater than 3.0 mm, less than 10 mm in CT imaging. c). For lymph nodes in the cN0 group, we selected the indeterminateand benign lymph node group according to the European Thyroid Association (ETA) and the Korean Society of Thyroid Radiology (KSThR) guidelines (Fig. 1).

Fig. 1
figure 1

The workflow of LNs enrollment

Study deign

In this study, thelymph nodes were from two centers: lymph nodesfrom center 1were divided into two cohorts according to the proportion of 7:3, one cohorts was used to established a radiomics prediction model we called radiomics score (Rad-score), one cohortswas used as an internal validation group; lymph nodesfrom center 2 were used as external validation group; Then the Rad-score is used to diagnose LN metastasis in cN0 goup. The CN0 group was additionally selected from Center 1.

CT protocol

All patients underwent contrast-enhanced neck CT, within one month before operation. The details of the CT protocol are indicated in the supplemental data (Appendix 1).

Radiomics analysis based on CT images

Image segmentation

Arterial phase CT images were retrieved from PACS and then exported to an open-source software (ITK-SNAP 3.8.0; www.itksnap.org) for segmentation. A total of 402 ROIs from were manually delineated into arterial phase CT images, by two independent readers, to evaluate the inter-observer reproducibility of the feature extraction. Three months after the initial segmentation, 50 ROIs from were selected randomly to be re-delineated by the same radiologist to analyze the intra-observer reproducibility of the feature extraction.

Radiomic feature extraction

A total of 396 radiomics features were automatically generated using AK software (Artificial Intelligence Kit, AK, GE Healthcare, China), which included a first order histogram, high order texture and morphological features (Supplemental Data, Appendix 2).

Feature selection and Modeling

In order to ensure repeatability and robustness of the model, features with ICC > 0.75 in both inter- and intra-reader agreement assessments were considered stable and remained for subsequently analysis. The remaining radiomics features were normalized by z-score method, and the abnormal numbers were replaced by a median value. In order to reduce overfitting of the model, high-dimensions of features were pre-selected with Kruskal-Wallis test. Thereafter, the least absolute shrinkage and selection operator (LASSO) regression with 10-fold cross-validation was repeated by a hundred times to select the most useful predictive radiomics features with non-zero coefficient in the training cohort. Upon conclusion of these steps, a Rad-score was calculated for each LN by linear combination of the selected features that were weighted with their respective coefficients. Then, the radiomics score formula derived from the training set was applied to internal validation group (from center #1) and external validation group (from center #2).

Performance evaluation in cN0 PTC patients

The performance of the Rad-score was tested in an independent validation cohort composed of cN0 PTC patients. We selected some lymph nodes with N1 and N0 by postoperative paraffin pathology, but whosepreoperative clinical stage was cN0in Center #1. All lymph nodes were identified on CT images by thyroid surgeons. All the central LNs of all patients were manually depicted as ROI by reader 1 according to the above mentioned criteria. Then extract the specified features of each ROI and use Rad-score for diagnosis LNs status.

Statistical analysis

Statistical analysis was conducted with R software (version 3.4.1; http://www.Rproject.org). Statistical tests were 2-sided, and a P-value of < 0.05 indicated statistical significance. The names of the R packages used for analyses were as follow: ICC was calculated using “lme4” package. LASSO regression analysis was performed using the “glmnet” package. Multivariate logistic regression were performed using the “rms” package. ROC curves were plotted using the “pROC” package. Delong test was used to compare the AUC values of training set, test sets and cN0 group. Decision curve analysis was performed using the “dca. R” package. Calibration curve and Hosmer-Lemeshow test were conducted using the “ModelGood” package.

Results

Baseline characteristics

The process of patient recruitment is illustrate in Fig. 1. According to the inclusion criteria, 133 PTC patients (male, n = 41; female, n = 92) in Center #1 (China-Japan union hospital of Jilin University) and 38 PTC patients (male, n = 9; female, n = 29) in Center #2 (The People’s Hospital of Bao’an) were selected. The clinical characteristics of these patients are shown in Table 1, while the baseline characteristics of the total enrolled LNs (n = 548) are presented in Table 2.

Table 1 Patient characteristics in Hospital 1 and Hospital 2
Table 2 Lymph node characteristics

Statistical analysis

Receiver operating characteristic (ROC) curves were plotted to evaluate the diagnostic performance of the radiomics score in both training and testing sets. Area under the ROC curve (AUC) with 95% confidence interval (CI), specificity, sensitivity, and accuracy were calculated. DeLong test was used to compare the differences of AUC values between different models in the training and testing set. To evaluate whether the models were well-calibrated or not, calibration curves were plotted in both training and testing sets. Decision curve analysis (DCA) was conducted to determine the clinical usefulness of the models by quantifying the net benefits at different threshold probabilities in both training and testing sets.

Development of the Radiomics Model

A total of 82 radiomics features, with ICC > 0.75 for both intra- and inter-observer reproducibility, were selected for further analysis. A number of radiomics features (n = 14) remained upon Kruskal-Wallis test and LASSO regression (Fig. 2), while 8 features were retained after multivariate logistic regression analysis, using backward stepwise elimination method. This latest approach was used to build a Rad-score via a linear combination weight with respective coefficient (Appendix 3). The formula utilized was as it follows:

Fig. 2
figure 2

A number of radiomics features remained upon Kruskal-Wallis test and LASSO regression

Radscore = 8.90*GLCMEnergy_angle0_offset1+-4.57*GLCMEntropy_AllDirection_offset7 + 1.01*HaralickCorrelation_angle0_offset1 + 6.41*differenceEntropy +-3.53*LowGreyLevelRunEmphasis_angle0_offset1 + 9.82*RunLengthNonuniformity_AllDirection_offset1_SD+-3.22*Compactness2 + 3.20*Sphericity+-9.05.

Validation of the Radiomics score

The radiomics score showed good performance to discriminate LN metastasis with AUC of 0.917(95% CI, 0.884 to 0.950), 0.892 (95% CI, 0.833 to 0.950) and 0.921 (95% CI, 868 to 0.973) in the training, internal validation cohort and external validation cohort, respectively. The test group of CN0 with a AUC of 0.892 (95% CI, 0.805 to 0.979) (Fig. 3). The accuracy was 85.4% (sensitivity = 81.3%; specificity = 88.9%) in the training cohort, 82.9% (sensitivity = 79.0%; specificity = 88.7%) in the internal validation cohort, 85.4% (sensitivity = 89.7%; specificity = 83.8%) in the external validation cohort, 86.7% (sensitivity = 83.8%; specificity = 91.3%) in the CN0 test group (Table 3).

Fig. 3
figure 3

The radiomics score showed good performance to discriminate LN metastasis with AUC of 0.917(95% CI, 0.884 to 0.950), 0.892 (95% CI, 0.833 to 0.950) and 0.921 (95% CI, 868 to 0.973) in the training, internal validation cohort and external validation cohort, respectively. The test group of CN0 with a AUC of 0.892 (95% CI, 0.805 to 0.979)

Table 3 The performance of radiomic score for predicting the status of LN in different datasets

The H-L test p-value was 0.805,0.698,0.725 and 0.204 in training cohort, internal and external validation cohort, CN0 test group, respectively, indicating fitness of the Rad-score (Fig. 4). The decision curve analysis showed the clinical usefulness of the radiomics model (Fig. 5). The distribution of radiomic score in different datasets was shown in Fig. 6; Table 4.

Fig. 4
figure 4

The H-L test p-value was 0.805, 0.698, 0.725 and 0.204 in training cohort, internal and external validation cohort, CN0 test group, respectively, indicating fitness of the Rad-score

Fig. 5
figure 5

The decision curve analysis showed the clinical usefulness of the radiomics model

Fig. 6
figure 6

The distribution of radiomic score in different datasets

Table 4 The distribution of radiomic score in different datasets

Discussion

Our study has presently developed and validated a CT-based radiomics model for preoperative prediction of the status of cN0 in PTC patients, using representative cohorts from two independent centers. In this context, radiomic nomogram was able to provide a potential non-invasive tool for the preoperative individualized prediction of the status of cN0 in PTC.

CT images were used to extract radiomics features to established radiomics model. Although, the most common method of cervical lymph node detection is ultrasound, however, due to the presence of sternum, US has limitations in imaging LNs in the retrosternal, and mediastinum, which restricting the detection of LNs in the central group, however, central group lymph nodes are sentinel nodes in thyroid cancer. Moreover, ultrasound diagnosis is highly dependent on personal operation, which possibly influences its reliability and reproducibility [19]. Some studys showed that CT has presented a significantly higher sensitivity and accuracy than US, but the sensitivity is still limited by 38.9–50% [12, 20,21,22,23,24,25,26,27]. Therefore, we chose to establish a CT based radiomics model. Our study have developed and validated a CT-based radiomics model with a with a balanced sensitivity (81.3%) and specificity (89.0%) in the training cohort, also have a good result in internal and external validation cohort. The results are better than Liu and colleagues’ radiomics model based on US(AUC = 0.782; ACC = 0.712) and Park and colleagues’ radiomics model based on US (AUC = 0.710 ). This indicates that our model has a good ability to predict the status of lymph nodes.

The diagnostic efficiency of the radiomics model we established is superior to other radiomics models based on CT, with AUCs of 0.917 and 0.921 in the training and external validation cohorts, a balanced sensitivity (81.3%) and specificity (89.0%) in the training cohort. Lu and colleagues established a radiomics model based on CT imaging, with the AUC of the training and validation cohorts were 0.867 and 0.822, a balanced sensitivity (72.4%) and specificity (76.3%) [28]. Zhou and colleagues established a radiomics model based on dual energy CT, with the AUC was 0.910 and 0.847 in the training and validation cohorts [29]. In their experiment, there was no restriction on the size of lymph nodes. Those lymph nodes larger than 1 cm in diameter were suggested to be metastasis by ultrasound, which indirectly increased the sensitivity of lymph node detection. In our study, we excluded lymph nodes larger than 1 cm in diameter. That is to say, the radiomics model we established had better performance in discriminating LN metastasis. Zhou and colleagues had a similar result to ours, however, it needs more data information, and the post-processing and operation process is relatively complex.

Moreover, our study predicts the CN0 and got a good result, with a AUC of 0.892 (95% CI, 0.805 to 0.979), a balanced sensitivity (83.8%) and specificity (91.3%). Although Fine-needle aspiration biopsy (FNAB)is the gold standard for the diagnosis of lymph node metastasis, one study showed FNAB had low sensitivity (11.94- 59.7%)and positive predictive value(15.69- 40.4%)for the diagnosis of indeterminate lymph nodes [30]. Our model has good detection efficiency to predict indeterminate lymph nodes, which may help to decrease the rate of unnecessary FNA for indeterminate LNs and improve the diagnosis of determinate lymph nodes. Therefore, our model can provide effective value for the diagnosis of cN0 status. This is also the innovation of our study.

In our study, the data was collected from two centers, improving the universality and reproducibility of our approach. This model was tested by a internal and external validation cohort (The external validation cohort is selected from center 2), indicating good robustness of the analysis. The CN0 test group is selected from center 1.

Nonetheless, our current study presents a few limitations. Firstly, this is a retrospective study, our data come from two centers, in which there may be some differences in CT images. Secondly, we did not incorporate clinical features to our model, since the cases we selected were too specific. Therefore, we will considered combining clinical risk factors to build the model. Our study did not include the basic CT image information into the model, because we studied clinically negative lymph nodes, and excluded those lymph nodes with obvious metastatic characteristics (maximal shortxis diameter, shape, margin, boundary, calcification, cystic change, necrosis, and enhancement, etc.).

Conclusion

In summary, a radiomics model based on preoperative CT images of LNs was presently designed. This radiomics model, constructed according to a machine learning method, shows great diagnostic potential to preoperatively predict the status of cN0 in PTC.

Data availability

All authors have reviewed the final version of the paper and would like to take public responsibility for its content.

Abbreviations

AUC:

Area under the curve

CND:

Central neck lymph node dissection

CT:

Computed tomography

DCA:

Decision curve analysis

H-L:

Hosmer-Lemeshow

ICC:

Intra/inter-class correlation coefficient

LASSO:

Least absolute shrinkage and selection operator

LN:

Lymph node

PTC:

Papillary thyroid carcinoma

Rad-score:

Radiomics score

ROC:

Receiver operating characteristic

ROI:

Region of interest

US:

Ultrasound

CN0:

Clinically node-negative

References

  1. Siegel R, Miller K, Jemal A. Cancer statistics, 2019. Cancer J Clin. 2019;69(1):7–34.

    Article  Google Scholar 

  2. Dralle H, Musholt T, Schabram J, Steinmüller T, Frilling A, Simon D, Goretzki P, Niederle B, Scheuba C, Clerici T, et al. German Association of Endocrine Surgeons practice guideline for the surgical management of malignant thyroid tumors. Langenbeck’s Archives Surg. 2013;398(3):347–75.

    Article  Google Scholar 

  3. Moo T, McGill J, Allendorf J, Lee J, Fahey T, Zarnegar R. Impact of prophylactic central neck lymph node dissection on early recurrence in papillary thyroid carcinoma. World J Surg. 2010;34(6):1187–91.

    Article  PubMed  Google Scholar 

  4. Haugen B, Alexander E, Bible K, Doherty G, Mandel S, Nikiforov Y, Pacini F, Randolph G, Sawka A, Schlumberger M, et al. 2015 American Thyroid Association Management Guidelines for adult patients with thyroid nodules and differentiated thyroid Cancer: the American Thyroid Association Guidelines Task Force on thyroid nodules and differentiated thyroid Cancer. Thyroid: Official J Am Thyroid Association. 2016;26(1):1–133.

    Article  Google Scholar 

  5. Haddad R, Nasr C, Bischoff L, Busaidy N, Byrd D, Callender G, Dickson P, Duh Q, Ehya H, Goldner W, et al. NCCN guidelines insights: thyroid carcinoma, Version 2.2018. J Natl Compr Cancer Network: JNCCN. 2018;16(12):1429–40.

    Article  Google Scholar 

  6. Filetti S, Durante C, Hartl D, Leboulleux S, Locati L, Newbold K, Papotti M, Berruti A. Thyroid cancer: ESMO Clinical Practice guidelines for diagnosis, treatment and follow-up†. Annals Oncology: Official J Eur Soc Med Oncol. 2019;30(12):1856–83.

    Article  CAS  Google Scholar 

  7. Yoo B, Song C, Ji Y, Lee J, Park H, Tae K. Efficacy of Central Neck dissection for clinically node-negative papillary thyroid carcinoma: Propensity Scoring Matching. Front Endocrinol. 2019;10:172.

    Article  Google Scholar 

  8. Sun W, Lan X, Zhang H, Dong W, Wang Z, He L, Zhang T, Liu S. Risk factors for Central Lymph Node Metastasis in CN0 papillary thyroid carcinoma: a systematic review and Meta-analysis. PLoS ONE. 2015;10(10):e0139021.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Lee D, Oh K, Cho J, Kwon S, Woo J, Baek S, Jung K. The Benefits and Risks of Prophylactic Central Neck Dissection for Papillary Thyroid Carcinoma: Prospective Cohort Study. International journal of endocrinology 2015, 2015:571480.

  10. de Carvalho AY, Chulam TC, Kowalski LP. Long-term results of Observation vs Prophylactic Selective Level VI Neck dissection for papillary thyroid carcinoma at a Cancer Center. Jama Otolaryngol. 2015;141(7):599–606.

    Google Scholar 

  11. Lu S, Zhao R, Ni Y, Ding J, Qiu F, Peng Y, Pan G, Wu F, Zhang Y, Shi J, et al. Development and validation of a nomogram for preoperative prediction of cervical lymph node involvement in thyroid microcarcinoma. Aging. 2020;12(6):4896–906.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Suh C, Baek J, Choi Y, Lee J. Performance of CT in the Preoperative Diagnosis of Cervical Lymph Node Metastasis in patients with papillary thyroid Cancer: a systematic review and Meta-analysis. AJNR Am J Neuroradiol. 2017;38(1):154–61.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Gillies R, Kinahan P, Hricak H. Radiomics: images are more than pictures, they are data. Radiology. 2016;278(2):563–77.

    Article  PubMed  Google Scholar 

  14. Kumar V, Gu Y, Basu S, Berglund A, Eschrich S, Schabath M, Forster K, Aerts H, Dekker A, Fenstermacher D, et al. Radiomics: the process and the challenges. Magn Reson Imaging. 2012;30(9):1234–48.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Liu Z, Wang S, Dong D, Wei J, Fang C, Zhou X, Sun K, Li L, Li B, Wang M, et al. The applications of Radiomics in Precision diagnosis and treatment of Oncology: opportunities and challenges. Theranostics. 2019;9(5):1303–22.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Wu S, Zheng J, Li Y, Yu H, Shi S, Xie W, Liu H, Su Y, Huang J, Lin T. A Radiomics Nomogram for the preoperative prediction of Lymph Node Metastasis in bladder Cancer. Clin cancer Research: Official J Am Association Cancer Res. 2017;23(22):6904–11.

    Article  CAS  Google Scholar 

  17. Xu L, Yang P, Liang W, Liu W, Wang W, Luo C, Wang J, Peng Z, Xing L, Huang M, et al. A radiomics approach based on support vector machine using MR images for preoperative lymph node status evaluation in intrahepatic cholangiocarcinoma. Theranostics. 2019;9(18):5374–85.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Liu T, Zhou S, Yu J, Guo Y, Wang Y, Zhou J, Chang C. Prediction of Lymph Node Metastasis in patients with papillary thyroid carcinoma: a Radiomics Method based on preoperative ultrasound images. Technol Cancer Res Treat. 2019;18:1533033819831713.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Lesnik D, Cunnane M, Zurakowski D, Acar G, Ecevit C, Mace A, Kamani D, Randolph G. Papillary thyroid carcinoma nodal surgery directed by a preoperative radiographic map utilizing CT scan and ultrasound in all primary and reoperative patients. Head Neck. 2014;36(2):191–202.

    Article  PubMed  Google Scholar 

  20. Lee Y, Kim JH, Baek JH, Jung SL, Park SW, Kim J, Yun TJ, Ha EJ, Lee KE, Kwon SY, et al. Value of CT added to ultrasonography for the diagnosis of lymph node metastasis in patients with thyroid cancer. Head Neck-J Sci Spec. 2018;40(10):2137–48.

    Article  Google Scholar 

  21. Lee D, Ji Y, Sung E, Park J, Lee Y, Park D, Tae K. Roles of ultrasonography and computed tomography in the surgical management of cervical lymph node metastases in papillary thyroid carcinoma. Eur J Surg Oncology: J Eur Soc Surg Oncol Br Association Surg Oncol. 2013;39(2):191–6.

    Article  CAS  Google Scholar 

  22. Kim E, Park J, Son K, Kim J, Jeon S, Na D. Preoperative diagnosis of cervical metastatic lymph nodes in papillary thyroid carcinoma: comparison of ultrasound, computed tomography, and combined ultrasound with computed tomography. Thyroid: Official J Am Thyroid Association. 2008;18(4):411–8.

    Article  CAS  Google Scholar 

  23. Kim S, Woo J, Park I, Lee J, Choe J, Kim J, Kim J. Computed Tomography-Detected Central Lymph Node Metastasis in Ultrasonography Node-negative papillary thyroid carcinoma: is it really significant? Ann Surg Oncol. 2017;24(2):442–9.

    Article  PubMed  Google Scholar 

  24. Yang S, Shin J, Hahn S, Lim Y, Hwang S, Kim T, Kim J. Comparison of ultrasonography and CT for preoperative nodal assessment of patients with papillary thyroid cancer: diagnostic performance according to primary tumor size. Acta Radiol (Stockholm Sweden: 1987). 2020;61(1):21–7.

    Google Scholar 

  25. Hwang H, Orloff L. Efficacy of preoperative neck ultrasound in the detection of cervical lymph node metastasis from thyroid cancer. Laryngoscope. 2011;121(3):487–91.

    Article  PubMed  Google Scholar 

  26. Khokhar M, Day K, Sangal R, Ahmedli N, Pisharodi L, Beland M, Monchik J. Preoperative High-Resolution Ultrasound for the Assessment of Malignant Central Compartment Lymph nodes in papillary thyroid Cancer. Thyroid: Official J Am Thyroid Association. 2015;25(12):1351–4.

    Article  Google Scholar 

  27. Lee Y, Kim D, Park H, Kim D, Jung S, Oh M, Bae S. Pre-operative ultrasound diagnosis of nodal metastasis in papillary thyroid carcinoma patients according to nodal compartment. Ultrasound Med Biol. 2015;41(5):1294–300.

    Article  PubMed  Google Scholar 

  28. Lu W, Zhong L, Dong D, Fang M, Dai Q, Leng S, Zhang L, Sun W, Tian J, Zheng J, et al. Radiomic analysis for preoperative prediction of cervical lymph node metastasis in patients with papillary thyroid carcinoma. Eur J Radiol. 2019;118:231–8.

    Article  PubMed  Google Scholar 

  29. Zhou Y, Su G, Hu H, Ge Y, Si Y, Shen M, Xu X, Wu F. Radiomics analysis of dual-energy CT-derived iodine maps for diagnosing metastatic cervical lymph nodes in patients with papillary thyroid cancer. Eur Radiol. 2020;30(11):6251–62.

    Article  CAS  PubMed  Google Scholar 

  30. Chung S, Baek J, Choi Y, Sung T, Song D, Kim T, Lee J. Risk factors for metastasis in indeterminate lymph nodes in preoperative patients with thyroid cancer. Eur Radiol. 2022;32(6):3863–8.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

This research was funded by Jilin Provincial Department of science and technology (20200403129SF), Health and Technology Development Program of Jilin Province (2021LC027), Jilin Province Finance and Health Talent Special Project (2022SCZ12), and Jilin Province Finance and Health Talent Special Project (2021SCZ37).

Author information

Authors and Affiliations

Authors

Contributions

Le Zhou and Mengchao Zhang conceived of and designed the study; Yifan Zhong and Zongbao Li collected and analysed the data and wrote the initial draft of the paper; Jianzhong Zheng and Yu Hu contributed to the acquisition, analysis, or interpretation of data; Yan Guo conducted the statistical analysis; Yanyan Yang, Yunxi Li, Meng Sun and Siqian Liu polished the language of the manuscript; All authors approved of the final version before submission.

Corresponding authors

Correspondence to Mengchao Zhang or Le Zhou.

Ethics declarations

Ethics approval and consent to participate

Ethics license was received from the Science Ethics Committee. This study is a retrospective study and informed consents were waived.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

The original online version of this article was revised: Following publication of the original article, we were notified that the correct affiliation of co-corresponding author Le Zhou is the Department of Thyroid Surgery, China-Japan Union Hospital of Jilin University, Changchun, 130000, China, rather than the Department of Radiology. Le Zhou is working in the thyroid surgery department.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary Material 1

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Li, Z., Zhong, Y., Lv, Y. et al. A CT based radiomics analysis to predict the CN0 status of thyroid papillary carcinoma: a two- center study. Cancer Imaging 24, 62 (2024). https://doi.org/10.1186/s40644-024-00690-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s40644-024-00690-y

Keywords