Skip to main content

ORIGINAL RESEARCH article

Front. Oncol., 08 September 2022
Sec. Cancer Imaging and Image-directed Interventions

Dual-layer dual-energy CT for improving differential diagnosis of squamous cell carcinoma from adenocarcinoma at gastroesophageal junction

Meihong Wu&#x;Meihong Wu1†Mao Sheng&#x;Mao Sheng1†Ruomei Li&#x;Ruomei Li1†Xinna ZhangXinna Zhang2Xingbiao ChenXingbiao Chen3Yin LiuYin Liu1Bin LiuBin Liu2Yongqiang YuYongqiang Yu2Xiaohu Li*Xiaohu Li2*
  • 1Department of Radiology, The Second People’s Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University, Hefei, China
  • 2Department of Radiology, Research Center of Clinical Medical Imaging, Anhui Province Clinical Image Quality Control Center, The First Affiliated Hospital of Anhui Medical University, Hefei, China
  • 3Clinical Science, Philips Healthcare, Shanghai, China

Objective: To examine the clinical values of dual-energy CT parameters derived from dual-layer spectral detector CT (SDCT) in the differential diagnosis of squamous cell carcinoma (SCC) and adenocarcinoma (AC) of the gastroesophageal junction (GEJ).

Methods: Totally 66 patients with SCC and AC of the GEJ confirmed by pathological analysis were retrospectively enrolled, and underwent dual-phase contrast-enhancement chest CT with SDCT. Plain CT value, CT attenuation enhancement (△CT), iodine concentration (IC), spectral slope (λHU), effective atomic number (Zeff) and 40keV CT value (CT40keV) of the lesion in the arterial phase (AP) and venous phase (VP) were assessed. Multivariate logistic regression analysis was performed to evaluate the diagnostic efficacies of different combinations of dual-energy CT parameters. Receiver operating characteristic (ROC) curves were used to analyze the accuracy of dual-energy CT parameters and Delong test was used to compare AUCs.

Results: IC, λHU, Zeff and CT40keV in AP and VP and △CT in VP were significantly higher in the AC group than those in the SCC group (all P<0.05). ROC curve analysis showed that IC, λHU, Zeff and CT40keV in VP had high diagnostic performances, with AUCs of 0.74, 0.74, 0.79 and 0.78, respectively. Logistic regression showed the combination of ICVP, λHU VP, CT40keV VP and Zeff VP had the highest AUC (0.84), with a threshold of 0.40, sensitivity and specificity in distinguishing SCC and AC were 93.1% and 73.0%, respectively. Delong test showed that the AUC of △CTVP was lower than other AUCs of dual-energy CT parameters.

Conclusion: Dual-energy CT parameters derived from SDCT provide added value in the differential diagnosis of SCC and AC of the GEJ, especially the combination of IC, λHU, CT40keV and Zeff in VP.

Advances in knowledge: Dual-energy CT parameters derived from dual-layer spectral detector CT provide added value to differentiate AC from SCC at the GEJ, especially the combination of effective atomic number, spectral slope, iodine concentration and 40keV CT value in VP.

Introduction

In recent years, the incidence of carcinoma of the gastroesophageal junction (GEJ), with the tumor center located within 5cm above or below the gastroesophageal junction and crossing or touching the GEJ, has shown a clear upward trend worldwide (13). In comparison to gastric or esophageal cancer, lymph node and hematogenous metastases are more likely to occur from GEJ cancer (4). In addition, the early postoperative recurrence rate is high, and patient prognosis is poor. Recent evidence from the American Joint Committee on Cancer Staging System suggests that SCC of the GEJ shows different clinicopathologic characteristics compared to AC (5). Previous studies (6, 7) have shown mediastinal lymph node metastases are more likely to occur in SCC above the GEJ, whereas metastases from the AC under the GEJ probably appear in the abdomen. It was reported that patient with AC had better prognosis performance than with SCC. The 10-year overall survival rate is >40% and about 20% in AC and SCC, respectively (8). In general, the clinicopathological classification of GEJ cancer is an independent prognostic factor that can affect the surgical pathway and lymph node dissection. So, it is particularly important to differentiate and diagnose SCC and AC accurately at the GEJ.

Relying on the fact that the x-ray attenuation was determined by the material composition, the mass density of the material, and the photon energies, dual-energy CT (DECT) was proposed to provide additional information (9). The main commercially available approaches of dual-energy CT are: rapid tube voltage switching DECT (rsDECT), dual-source DECT (dsDECT) and dual-layer spectral detector CT (SDCT). Many clinical applications and software tools with DECT were developed for use (e.g., isoattenuating gallstones identification, virtual non-calcium maps) (9, 10). SDCT is the latest detector-based dual-energy CT which uses two layers of detectors to separate high- and low energy level x-ray attenuation (9, 10). It can provide both conventional images and several spectral image series from a single acquisition. The spectral image series can provide more quantitative indicators to show microscopic changes in the tumor’s internal tissue structure and hemodynamics. However, few reports have reported these clinical benefits in assessment of GEJ cancer. Zhou Yue et al. (11) reported that the combination of normalized iodine concentration and spectral slope from 40-70 keV in arterial phase (AP) was of great value in differentiating SCC from AC of the GEJ. Ma Yi-Chuan et al. (12) reported that effective atomic number (Zeff) in venous phase (VP) had the highest diagnostic efficiency for differentiating SCC and AC of the GEJ. The same rsDECT was used in both studies but with different research outputs.

The purpose of this study was to investigate the clinical values of DECT parameters derived from SDCT in the differential diagnosis of AC and SCC of the GEJ.

Methods

The institutional review board approved this retrospective study and waived the requirement for written informed consent.

Patients

The clinical and imaging data of 66 patients with pathologically confirmed AC or SCC of the GEJ in our hospital from February to December 2021 were retrospectively collected. Age, sex, pathological type, degree of differentiation, main clinical symptoms and lesion locations were recorded. Inclusion criteria were: (1) cancer located at the GEJ; (2) AC or SCC of the GEJ confirmed by postoperative pathology or gastroscopic biopsy; (3) spectral enhanced chest CT performed before surgery. Exclusion criteria were: (1) incomplete clinical or imaging data; (2) other related treatments before DECT examination.

Dual-energy CT examination

All patients underwent SDCT (IQon, Philips Healthcare, Best, the Netherlands), two-phase enhanced chest scan before the treatment. The scan range was from the thoracic inlet to the bottom of the lung. The major scan parameters were: tube voltage, 120 kVp; automatic tube current modulation (tube current-time product 74 mAs to 120 mAs); slice thickness and spacing, 5.0 mm; X-ray tube rotation time, 0.5 s; detector collimation, 64x0.625 mm; pitch, 0.516; field-of-view (FOV), 350mm; reconstruction matrix, 512x512. A high-pressure syringe was utilized to inject 60-80 ml of contrast media (iodixanol, 320 mg iodine/mL) through the cubital vein at a flow rate of 3.0 ml/s. The bolus tracking technology was used, and the arterial and venous phases were started 30 and 60 s after injection, respectively. After scanning, both conventional 120 kVp images and spectral based images (SBIs) were reconstructed. The mean effective radiation dose (ED) of patients is (12.42 ± 2.41) mSv.

Measurement of quantitative dual-energy CT parameters

All images were transferred to the dedicated post-processing workstation (IntelliSpace Portal, version 10.0; Philips Healthcare). Plain CT value, CT attenuation enhancement (△CT), iodine concentration value (IC), spectral slope (λHU), effective atomic number (Zeff) and CT value at the energy level of 40 keV (CT40keV) for each lesion in AP and VP were measured. A region of interest (ROI) was placed in the solid component of the lesion in the axial image (with covering >70% in the maximum section, 15-196 mm2), and blood vessels, necrotic cystic areas, hemorrhage and calcification areas were avoided as much as possible. All the positions of ROIs delineated on the images of the same lesion at each phase were consistent. Each measurement was repeated three times and averaged. Then, △CT and λHU were calculated by the following formulae (13):

CT attenuation enhancement:ΔCTAP/VP= CTAP/VPCTPlain scan
Spectral slope: λHU=(CT40keV-CT100 keV)/60

Statistical analysis

SPSS 22.0 (SPSS, USA) was used for data analysis. Continuous variables were expressed as mean ± standard deviation (SD). Normally distributed data were compared by the independent samples t test between the SCC and AC groups; a non-parametric test was used for non-normally distributed data. The Chi-squared test or the Fisher’s exact probability method was used for comparing categorical data. Multivariate logistic regression analysis was performed for variables with P<0.05 in univariate analysis and predicted probabilities were recorded for further receiver operating characteristic (ROC) curve analysis. ROC curve analysis was performed to evaluate the diagnostic efficacy and Youden index was calculated to determine the optimal diagnostic threshold. Delong test was used to compare AUCs. P<0.05 was considered statistically significant.

Results

Patient features

A total of 66 patients (mean age, 74 ± 9 years; 50 men) were enrolled in this study, including 37 AC and 29 SCC cases. Among them, 22 and 44 cases were confirmed by pathology after surgery and gastroscopic biopsy, respectively. There were no significant differences in patient age, gender, tumor location, degree of differentiation and clinical symptoms between the two groups (all P>0.05), as shown in Table 1.

TABLE 1
www.frontiersin.org

Table 1 Clinical data of the included patients.

Imaging manifestation of GEJ cancer

Patients with AC or SCC groups had irregular wall thickening at the GEJ, varying degrees of luminal stenosis, and partial formation of soft tissue mass, which showed moderate to obvious uneven enhancement on enhanced CT images (Figures 1, 2). The average diameters of the lesions in AC group and SCC group were about 30.52 ± 10.32mm and 29.61 ± 8.85mm, respectively. Lymph node enlargement was observed in 16 AC and 6 SCC cases from the cardia or lesser curvature of the stomach; 8 AC and 4 SCC cases showed multiple liver metastasis; 3 AC and 8 SCC cases had adrenal metastasis and mediastinal lymph node enlargement, respectively.

FIGURE 1
www.frontiersin.org

Figure 1 Dual-energy CT findings of venous phase AC of the GEJ. A male patient, 68 years old, was confirmed with AC of the GEJ by postoperative pathology. (A) Conventional CT image showing irregular thickening of the wall of the GEJ, luminal stenosis, and obvious enhancement in the venous phase. (B) 40keV virtual monochromatic image showing a CT attenuation value of the lesion in the venous phase of 312.3 HU. (C) The IC of the solid component of the lesion was3.14 mg/ml. (D) The Zeff of the lesion was 8.87. (E) Hematoxylin-eosin staining of AC with ×100 magnification.

FIGURE 2
www.frontiersin.org

Figure 2 Dual-energy CT findings of venous phase SCC of the GEJ. A male patient, 78 years old, was confirmed with SCC of the GEJ by postoperative pathology. (A) Conventional CT image showing irregular thickening of the wall of the GEJ, luminal stenosis, and moderate enhancement in the venous phase. (B) 40keV virtual monochromatic image revealed a CT attenuation value of the lesion in the venous phase of 126.4 HU. (C) The IC of the solid component of the lesion was 0.92mg/ml. (D) The Zeff of the lesion was 7.83. (E) Hematoxylin-eosin staining of SCC with ×100 magnification.

Quantitative dual-energy CT parameters comparison

There was no significant difference in △CT in AP between the AC and SCC groups (P=0.065). IC, λHU, Zeff and CT40keV in AP and VP, and △CT in VP from AC group were significantly higher than those from SCC group (all P<0.05), as shown in Table 2 and Figure 3. ROC curve analysis showed that the diagnostic efficiencies of IC, λHU, Zeff and CT40keV were higher in VP compared with the AP, with AUCs of 0.74, 0.74, 0.79 and 0.78, respectively. The prediction probabilities from multivariate logistic regression analysis of IC, λHU, Zeff and CT40keV in VP reach the highest AUC (0.84) with a threshold of 0.40, sensitivity and specificity for SCC and AC detection were 93.1% and 73.0%, respectively (Figure 4). Detailed results of ROC analysis were listed in Table 3. Delong test showed that the AUC of △CTVP was significantly lower than that of combination (ICVP, λHU VP, CT40keV VP and Zeff VP), P<0.05.

TABLE 2
www.frontiersin.org

Table 2 Dual-energy CT parameters in the AC and SCC groups in AP and VP.

FIGURE 3
www.frontiersin.org

Figure 3 (A–E) Box plots of dual-energy CT parameters in AP and VP. ΔCT, IC, λHU, Zeff, and CT40keV in AP and VP are higher for AC compared with SCC, to varying degrees, with differences in energy Dual-energy CT parameters greater in VP than in AP.

FIGURE 4
www.frontiersin.org

Figure 4 IC, λHU, Zeff, CT40keV, Combination ROC curve in VP. The combination of IC, λHU, CT40keV and Zeff in VP had the highest diagnostic efficacy.

TABLE 3
www.frontiersin.org

Table 3 Differential diagnostic efficacies of Dual-energy CT parameters in AP and VP.

Discussion

Due to the particularities of tumor sites, there are great differences in clinical stages and treatment planning for GEJ tumors. In order to clarify the definition of cancer of the esophagogastric junction and design the therapeutic strategy, Siewert and colleagues published a topographic-anatomic subclassification of adenocarcinomas of the EGJ in 1987 (14). This classification was approved at the consensus meetings of the International Society of Diseases of the Esophagus in 1995 and the International Gastric Cancer Association in 1997 (15). The Siewert classification is purely based on the anatomic localization of the tumor center, which can be defined by endoscopy using the proximal end of the longitudinal gastric mucosa folds as a pragmatic reference for the endoscopic cardia (zero point). Siewert classification of adenocarcinomas of the esophagogastric junction. Siewert I: tumor center 1 cm above to 5 cm above the cardia (zero point). Siewert II: tumor center 1 cm above to 2 cm below the cardia (zero point). Siewert III: tumor center 5 cm below to 2 cm below the cardia (zero point) (14).

In general, Siewert I cancer is epidemiologically and histologically similar to esophageal cancer, which should refer to the clinical staging and surgical strategy of esophageal cancer. While Siewert II and III are epidemiologically and histologically similar to gastric cancer., which should refer to the clinical staging and surgical strategy of gastric cancer (16). Researchers have found that the three Siewert types in Western countries mainly include AC cases, while in Eastern countries Siewert type I mainly comprises SCC cases, and type II and III mainly have AC cases (16, 17). Therefore, better differentiation between SCC and AC at the GEJ would be helpful for clinical stages and treatment plan development. Moreover, a large number of studies have revealed that low-level virtual monochromatic imaging and iodine density fusion imaging can significantly improve the contrast between tumor lesions and surrounding tissues, which enhances lesion visualization and provides added value for clinical staging and Siewert classification of GEJ carcinoma.

The current study showed that dual-energy CT parameters in VP had better differential diagnosis efficiency between SCC and AC than those obtained in AP, and dual-energy CT parameters performed better than conventional CT attenuation enhancement (AUC values of 0.74-0.79 vs 0.69). Interestingly, the combination of IC, λHU, Zeff and CT40keV in VP had the highest AUC (0.84). The possible reason is that CT scan in AP is performed earlier, with insufficient iodine uptake by the lesions, while perfusion in VP is more adequate (12). The diagnostic efficacy in this study was similar to that described by a previous study by Zhou Yue et al. (11) with the highest AUC of 0.804. However, the latter study showed that the AUCs of normalized iodine concentration (NIC), λ40-70keV and Zeff in AP was higher in AC group than those in SCC group, and the combined diagnosis efficiency of NIC and λ40-70keV in AP had the highest AUC (0.804). The main reason for this discrepancy might be the different DECT scanners and scan protocols used. Nevertheless, the previous two studies and ours showed the clinical benefits derived from DECT parameters in differentiating SCC from AC and further studies with large cohorts of patients should performed.

The iodine density map in Dual-energy CT mainly reflects the blood supply status of the lesion; the higher the IC value, the richer the lesion’s blood supply (18). The above results showed that the IC values of AC of the GEJ in AP and VP were higher than those of SCC, indicating that AC has higher vascularity than SCC. The possible reason is that AC grows diffusely in the wall, and the internal pressure of the tissue is small, which promotes growth and opening of new blood vessels, while SCC shows continuous-accumulation growth, which does not promote the growth and development of new blood vessels (19). The current results corroborated a study on lung AC and SCC (20). Effective atomic number reflects the material’s composition, which can be used for lesion detection or differentiation (21). In this study, Zeff in VP had the highest diagnostic performance, with an AUC of 0.79 in differentiating AC and SCC, corroborating low-energy level (e.g., 40keV) virtual monochromatic imaging can significantly improve the CT attenuation of lesions containing a contrast agent, which is helpful for lesion detection, tumor delineation and artery assessment (21). As shown above, the CT40keV values of AC in AP and VP were higher than those of SCC, also resulting in a good AUC of 0.78 in VP.

This study had some limitations. First, the sample size was relatively small. Secondly, metastatic lymph nodes were not further analyzed. Thirdly, the microvessels of tumors were not confirmed, and correlations with DECT parameters were not analyzed.

In conclusion, dual-energy CT parameters derived from dual-layer spectral detector CT provide added value to differentiate AC from SCC at the GEJ, especially the combination of effective atomic number, spectral slope, iodine concentration and 40-keV CT value in VP.

Data availability statement

The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author.

Ethics statement

The studies involving human participants were reviewed and approved by The Second People’s Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University review board approved this retrospective study and waived the requirement for written informed consent. The ethics committee waived the requirement of written informed consent for participation.

Author contributions

All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.

Conflict of interest

Author XC was employed by Philips Healthcare.

The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Abbreviations

GEJ, gastroesophageal junction; SDCT, Dual-layer spectral detector CT; SCC, squamous cell carcinoma; AC, adenocarcinoma.

References

1. Chau I, Bendell JC, Calvo E, Santana-Davila R, Ahnert JR, Penel N, et al. Interim safety and clinical activity in patients (pts) with advanced gastric or gastroesophageal junction (G/GEJ) adenocarcinoma from a multicohort phase 1 study of ramucirumab (R) plus pembrolizumab (P). J Clin Oncol (2017) 35(4_suppl):102–2. doi: 10.1200/JCO.2017.35.4_suppl.102

CrossRef Full Text | Google Scholar

2. Koeter M, Parry K, Verhoeven RH, Luyer MD, Ruurda JP, van Hillegersberg R, et al. Perioperative treatment, not surgical approach, influences overall survival in patients with gastroesophageal junction tumors: A nationwide, population-based study in the netherlands. Ann Surg Oncol (2016) 23(5):1632–8. doi: 10.1245/s10434-015-5061-7

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Yuan Y, Chen X, Hu J, Chen L. [Interpretation of Chinese expert consensus on the surgical treatment for adenocarcinoma of esophagogastric junction (2018 edition)]. Zhonghua Wei Chang Wai Ke Za Zhi (2019) 22(2):101–6. doi: 10.3760/cma.j.issn.1671⁃0274.2019.02.001

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Lerut T, Moons J, Coosemans W, Van Raemdonck D, De Leyn P, Decaluwe H, et al. Postoperative complications after transthoracic esophagectomy for cancer of the esophagus and gastroesophageal junction are correlated with early cancer recurrence: role of systematic grading of complications using the modified clavien classification. Ann Surg (2009) 250(5):798–807. doi: 10.1097/SLA.0b013e3181bdd5a8

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Moureau-Zabotto L, Teissier E, Cowen D, Azria D, Ellis S, Resbeut M. Impact of the siewert classification on the outcome of patients treated by preoperative chemoradiotherapy for a nonmetastatic adenocarcinoma of the oesophagogastric junction. Gastroenterol Res Pract (2015) 2015:404203. doi: 10.1155/2015/404203

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Huang Q. Carcinoma of the gastroesophageal junction in Chinese patients. World J Gastroenterol (2012) 18(48):7134–40. doi: 10.3748/wjg.v18.i48.7134

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Giganti F, Ambrosi A, Petrone MC, Canevari C, Chiari D, Salerno A, et al. Prospective comparison of MR with diffusion-weighted imaging, endoscopic ultrasound, MDCT and positron emission tomography-CT in the pre-operative staging of oesophageal cancer: Results from a pilot study. Br J Radiol (2016) 89(1068):20160087. doi: 10.1259/bjr.20160087

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Siewert JR, Ott K. Are squamous and adenocarcinomas of the esophagus the same disease? Semin Radiat Oncol (2007) 17(1):38–44. doi: 10.1016/j.semradonc.2006.09.007

PubMed Abstract | CrossRef Full Text | Google Scholar

9. McCollough CH, Boedeker K, Cody D, Duan X, Flohr T, Halliburton SS, et al. Principles and applications of multienergy CT: Report of AAPM task group 291. Med Phys (2020) 47(7):e881–912. doi: 10.1002/mp.14157

PubMed Abstract | CrossRef Full Text | Google Scholar

10. McCollough CH, Leng S, Yu L, Fletcher JG. Dual- and multi-energy ct: principles, technical approaches, and clinical applications. Radiology (2015) 276(3):637–53. doi: 10.1148/radiol.2015142631

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Zhou Y, Hou P, Zha K, Liu D, Wang F, Zhou K, et al. Spectral computed tomography for the quantitative assessment of patients with carcinoma of the gastroesophageal junction: Initial differentiation between a diagnosis of squamous cell carcinoma and adenocarcinoma. J Comput Assist Tomogr (2019) 43(2):187–93. doi: 10.1097/RCT.0000000000000826

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Ma YC, Zhang SH, Xie ZY, Guo F, Chen AQ. Comparison of spectral computed tomography imaging parameters between squamous cell carcinoma and adenocarcinoma at the gastroesophageal junction. Technol Health Care (2021) 29(4):619–27. doi: 10.3233/THC-202343

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Demirler Şimşir B, Krug KB, Burke C, Hellmich M, Maintz D, Coche E. Possibility to discriminate benign from malignant breast lesions detected on dual-layer spectral CT-evaluation. Eur J Radiol (2021), 142:109832. doi: 10.1016/j.ejrad.2021.109832

CrossRef Full Text | Google Scholar

14. Siewert JR, Holscher AH, Becker K, Gossner W. [Cardia cancer: attempt at a therapeutically relevant classification]. Chirurg (1987) 58(1):25–32.

PubMed Abstract | Google Scholar

15. Siewert JR, Stein HJ. Classification of adenocarcinoma of the oesophagogastric junction. Br J Surg (1998) 85(11):1457–9. doi: 10.1046/j.1365-2168.1998.00940.x

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Rice TW, Ishwaran H, Ferguson MK, Blackstone EH, Goldstraw P. Cancer of the esophagus and esophagogastric junction: An eighth edition staging primer. J Thorac Oncol (2017) 12(1):36–42. doi: 10.1016/j.jtho.2016.10.016

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Hosokawa Y, Kinoshita T, Konishi M, Takahashi S, Gotohda N, Kato Y, et al. Clinicopathological features and prognostic factors of adenocarcinoma of the esophagogastric junction according to siewert classification: Experiences at a single institution in Japan. Ann Surg Oncol (2012) 19(2):677–83. doi: 10.1245/s10434-011-1983-x

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Chen A, Liu A, Liu J, Tian S, Wang H, Liu Y. Application of dual-energy dual-energy CT imaging in differential diagnosis of bladder cancer and benign prostate hyperplasia. Med (Baltimore) (2016) 95(52):e5705. doi: 10.1097/MD.0000000000005705

CrossRef Full Text | Google Scholar

19. Li GJ, Gao J, Wang GL, Zhang CQ, Shi H, Deng K. Correlation between vascular endothelial growth factor and quantitative dual-energy dual-energy CT in non-small-cell lung cancer. Clin Radiol (2016) 71(4):363–8. doi: 10.1016/j.crad.2015.12.013

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Wang G, Zhang C, Li M, Deng K, Li W. Preliminary application of high-definition computed tomographic gemstone spectral imaging in lung cancer. J Comput Assist Tomogr (2014) 38(1):77–81. doi: 10.1097/RCT.0b013e3182a21633

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Rassouli N, Etesami M, Dhanantwari A, Rajiah P. Detector-based dual-energy CT with a novel dual-layer technology: principles and applications. Insights Imaging (2017) 8(6):589–98. doi: 10.1007/s13244-017-0571-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: dual-layer dual-energy CT, squamous cell carcinoma, gastroesophageal junction, adenocarcinoma, effective atomic number

Citation: Wu M, Sheng M, Li R, Zhang X, Chen X, Liu Y, Liu B, Yu Y and Li X (2022) Dual-layer dual-energy CT for improving differential diagnosis of squamous cell carcinoma from adenocarcinoma at gastroesophageal junction. Front. Oncol. 12:979349. doi: 10.3389/fonc.2022.979349

Received: 27 June 2022; Accepted: 08 August 2022;
Published: 08 September 2022.

Edited by:

Wenli Cai, Massachusetts General Hospital, Harvard Medical School, United States

Reviewed by:

Hongzan Sun, Shengjing Hospital of China Medical University, China
Xiaozhu Lin, Shanghai Jiao Tong University, China

Copyright © 2022 Wu, Sheng, Li, Zhang, Chen, Liu, Liu, Yu and Li. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Xiaohu Li, lixiaohu@ahmu.edu.com

These authors have contributed equally to this work

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.