AccScience Publishing / CP / Online First / DOI: 10.36922/CP026110015
ORIGINAL RESEARCH ARTICLE

Radial tumor thickness by endoscopic ultrasonography as a predictor of pathological complete response in esophageal squamous cell carcinoma

Hong-yu Chen1 Yu-fan Chen2,3,4 Qiao-na Liu2,3,4 Shi-yong Lin2,3,4 Xu Zhang2,3,5 Guang-yu Luo2,3,4*
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1 Department of Medical Oncology, The Second Affiliated Hospital of Guangxi University of Science and Technology, Liuzhou, Guangxi, China
2 State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China
3 Guangdong Provincial Clinical Research Center for Cancer, Collaborative Innovation Center for Cancer Medicine, Guangzhou, Guangdong, China
4 Department of Endoscopy, Endoscope Center, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China
5 Department of Thoracic Surgery, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China
Received: 15 March 2026 | Revised: 3 April 2026 | Accepted: 8 April 2026 | Published online: 19 May 2026
© 2026 by the Author(s). This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution 4.0 International License ( https://creativecommons.org/licenses/by/4.0/ )
Abstract

Pathological complete response (pCR) after neoadjuvant therapy is associated with improved prognosis, and reliable tools are needed to evaluate treatment response before surgery. Endoscopic ultrasonography (EUS) has been suggested as a more effective modality than computed tomography and white light endoscopy (WLE). A total of 139 patients with esophageal cancer—who received neoadjuvant therapy followed by surgery at Sun Yat-sen University Cancer Center, Guangzhou, China, between December 2006 and April 2022—were enrolled in this study. Each patient underwent EUS prior to surgery. EUS, WLE, and computed tomography scans were evaluated for features associated with pCR based on postoperative pathology. Of the 139 patients, 28 with severe esophageal stricture, three unable to tolerate examination, and two with adenocarcinoma were excluded. In the remaining 106 patients, univariate analysis showed that lesion length, maximal radial tumor thickness, T stage, and N stage (assessed by EUS), tumor macroscopic findings (WLE), biopsy results, tumor regression grade, and pathological T stage differed significantly. Furthermore, predictive performance analysis showed that EUS infiltration depth had the highest accuracy for predicting pCR, with an area under the curve of 0.79. A random forest model identified EUS infiltration depth as a key predictor. In conclusion, EUS infiltration depth after neoadjuvant therapy may predict pCR in patients with esophageal squamous cell carcinoma.

Keywords
Endoscopic ultrasonography
Neoadjuvant therapy
Pathological complete response
Esophageal squamous cell carcinoma
Infiltration depth
Funding
None.
Conflict of interest
The authors declare that they have no competing interests.
References
  1. Sung H, Ferlay J, Siegel R L, Laversanne M, Soerjomataram I, Jemal A, et al. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clinicians. 2021;71(3):209-249. doi: 10.3322/caac.21660
  2. Chen W, Zheng R, Baade PD, et al. Cancer statistics in China, 2015. CA Cancer J Clinicians. 2016;66(2):115-132. doi: 10.3322/caac.21338
  3. Pennathur A, Gibson MK, Jobe BA, Luketich JD. Oesophageal carcinoma. Lancet. 2013;381(9864):400-412. doi: 10.1016/s0140-6736(12)60643-6
  4. Luo H, Lu J, Bai Y, et al. Effect of Camrelizumab vs Placebo Added to Chemotherapy on Survival and Progression-Free Survival in Patients With Advanced or Metastatic Esophageal Squamous Cell Carcinoma: JAMA. 2021;326(10):916. doi: 10.1001/jama.2021.12836
  5. Liu G, Han Y, Peng L, Wang K, Fan Y. Reliability and safety of minimally invasive esophagectomy after neoadjuvant chemoradiation: a retrospective study. J Cardiothorac Surg. 2019;14(1). doi: 10.1186/s13019-019-0920-0
  6. Zhu J, Leng X, Gao B, et al. Efficacy and safety of neoadjuvant immunotherapy in resectable esophageal or gastroesophageal junction carcinoma: A pooled analysis of prospective clinical trials. Front Immunol. 2022;13. doi: 10.3389/fimmu.2022.1041233
  7. Meredith KL, Weber JM, Turaga KK, et al. Pathologic response after neoadjuvant therapy is the major determinant of survival in patients with esophageal cancer. Ann Surg Oncol. 2010;17(4):1159-1167. doi: 10.1245/s10434-009-0862-1
  8. Soror T, Kho G, Zhao KL, Ismail M, Badakhshi H. Impact of pathological complete response following neoadjuvant chemoradiotherapy in esophageal cancer. J Thorac Dis. 2018;10(7):4069-4076. doi: 10.21037/jtd.2018.06.85
  9. Jost C, Binek J, Schuller JC, et al. Endosonographic radial tumor thickness after neoadjuvant chemoradiation therapy to predict response and survival in patients with locally advanced esophageal cancer: a prospective multicenter phase ll study by the Swiss Group for Clinical Cancer Research (SAKK 75/02). Gastrointest Endosc. 2010;71(7):1114-1121. doi: 10.1016/j.gie.2009.12.015
  10. Noordman BJ, Spaander MCW, Valkema R, et al. Detection of residual disease after neoadjuvant chemoradiotherapy for oesophageal cancer (preSANO): a prospective multicentre, diagnostic cohort study. Lancet Oncol.2018;19(7):965-974. doi: 10.1016/s1470-2045(18)30201-8
  11. Cosgrove ND, Mullady DK. Endoscopic evaluation of the esophageal cancer patient after chemoradiotherapy for persistent/recurrent cancer. Dis Esophagus.2018;31(7). doi: 10.1093/dote/doy023
  12. Japan Esophageal S. Japanese Classification of Esophageal Cancer, 11th Edition: part II and III. Esophagus. 2017;14(1):37-65. doi: 10.1007/s10388-016-0556-2
  13. Donohoe CL, O’Farrell NJ, Grant T, et al. Classification of pathologic response to neoadjuvant therapy in esophageal and junctional cancer. Ann Surg. 2013;258(5):784-792. doi: 10.1097/SLA.0b013e3182a66588
  14. Ajani JA, D’Amico TA, Bentrem DJ, Chao J, Corvera C, Das P, et al. Esophageal and Esophagogastric Junction Cancers, Version 2.2019, NCCN Clinical Practice Guidelines in Oncology. J Natl Compr Cancer Netw. 2019;17(7):855-883. doi: 10.6004/jnccn.2019.0033
  15. Wu Y, Li J. Change in Maximal Esophageal Wall Thickness Provides Prediction of Survival and Recurrence in Patients with Esophageal Squamous Cell Carcinoma After Neoadjuvant Chemoradiotherapy and Surgery. CMAR. 2021;13:2433-2445. doi: 10.2147/CMAR.S295646
  16. Qiu B, Wang D, Yang H, et al. Combined modalities of magnetic resonance imaging, endoscopy and computed tomography in the evaluation of tumor responses to definitive chemoradiotherapy in esophageal squamous cell carcinoma. Radiother Oncol. 2016;121(2):239-245. doi: 10.1016/j.radonc.2016.09.017
  17. Chablaney S, Zator ZA, Kumta NA. Diagnosis and Management of Rectal Neuroendocrine Tumors. Clin Endosc. 2017;50(6):530-536. doi: 10.5946/ce.2017.134
  18. Wilk BJ, Eyck BM, Doukas M, et al. Residual disease after neoadjuvant chemoradiotherapy for oesophageal cancer: locations undetected by endoscopic biopsies in the preSANO trial. Br J Surg. 2020;107(13):1791-1800. doi: 10.1002/bjs.11760
  19. Yan Y, Wu Q, Li ZY, Bu ZD, Ji JF. Endoscopic ultrasonography for pretreatment T-staging of gastric cancer: An in vitro accuracy and discrepancy analysis. Oncol Lett. 2019;17(3):2849-2855. doi: 10.3892/ol.2019.9920
  20. Heneghan HM, Donohoe C, Elliot J, Ahmed Z, Malik V, Ravi N, et al. Can CT-PET and Endoscopic Assessment Post-Neoadjuvant Chemoradiotherapy Predict Residual Disease in Esophageal Cancer? Ann Surg. 2016;264(5):831-838. doi: 10.1097/SLA.0000000000001902
  21. van Rossum PSN, Goense L, Meziani J, et al. Endoscopic biopsy and EUS for the detection of pathologic complete response after neoadjuvant chemoradiotherapy in esophageal cancer: a systematic review and meta-analysis. Gastrointest Endosc.2016;83(5):866-879. doi: 10.1016/j.gie.2015.11.026
  22. van der Bogt RD, Noordman BJ, Krishnadath KK, et al. Endoscopic ultrasound measurements for detection of residual disease after neoadjuvant chemoradiotherapy for esophageal cancer. Endoscopy. 2019;51(4):326-332. doi: 10.1055/a-0795-3220
  23. Liu J, Zhang M, Zhu M, et al. Comparative analysis of diagnostic techniques and treatment modalities for early-stage esophageal carcinoma: a comprehensive review. Front Oncol. 2025;15. doi: 10.3389/fonc.2025.1650965
  24. Yonemoto S, Uesato M, Nakano A, et al. Why is endosonography insufficient for residual diagnosis after neoadjuvant therapy for esophageal cancer? Solutions using muscle layer evaluation. WJGE. 2022;14(5):320-334. doi: 10.4253/wjge.v14.i5.320
  25. Wang F, Guo R, Zhang, et al. Value of 18F-FDG PET/MRI in the Preoperative Assessment of Resectable Esophageal Squamous Cell Carcinoma: A Comparison With (18)F-FDG PET/CT, MRI, and Contrast-Enhanced CT. Front Oncol. 2022;12. doi: 10.3389/fonc.2022.844702
  26. Luo LN, He LJ, Gao XY, et al. Evaluation of preoperative staging for esophageal squamous cell carcinoma. WJG. 2016;22(29):6683. doi: 10.3748/wjg.v22.i29.6683
  27. Li X, Wang Y, Kong M, Lin J. Systematic review and meta-analysis of endoscopic ultrasonography in staging diagnosis of esophageal cancer after neoadjuvant radiotherapy and chemotherapy. J Gastrointest Oncol. 2022;13(4):1525-1540. doi: 10.21037/jgo-22-437
  28. Tirumani H, Rosenthal MH, Tirumani SH, Shinagare AB, Krajewski KM, Ramaiya NH. Esophageal Carcinoma: Current Concepts in the Role of Imaging in Staging and Management. Can Assoc Radiol J. 2015;66(2):130-139. doi: 10.1016/j.carj.2014.08.006
  29. Westerterp M, van Westreenen HL, Reitsma JB, et al. Esophageal Cancer: CT, Endoscopic US, and FDG PET for Assessment of Response to Neoadjuvant Therapy— Systematic Review. Radiology. 2005;236:841-851. doi: 10.1148/radiol.2363041042
  30. Beer AJ, Wider HA, Lordick F, et al. Adenocarcinomas of Esophagogastric Junction: Multi-Detector Row CT to Evaluate Early Response to Neoadjuvant Chemotherapy. Radiology. 2006;239(2):472-480. doi: 10.1148/radiol.2391050043
  31. Li Y, Yu M, Wang G, et al. Contrast-Enhanced CT-Based Radiomics Analysis in Predicting Lymphovascular Invasion in Esophageal Squamous Cell Carcinoma. Front Oncol. 2021;11. doi: 10.3389/fonc.2021.644165
  32. Shi P, Meng X, Ni M, Sun X, Xing L, Yu J. Association between serum tumor markers and metabolic tumor volume or total lesion glycolysis in patients with recurrent small cell lung cancer. Oncol Lett. 2015;10(5):3123-3128. doi: 10.3892/ol.2015.3673
  33. Li Y, Liu J, Li HX, et al. Radiomics Signature Facilitates Organ- Saving Strategy in Patients With Esophageal Squamous Cell Cancer Receiving Neoadjuvant Chemoradiotherapy. Front Oncol. 2021;10. doi: 10.3389/fonc.2020.615167
  34. Eisenhauer EA, Therasse P, Bogaerts J, et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer. 2009;45(2):228-247. doi: 10.1016/j.ejca.2008.10.026
  35. Jain RK, Lee JJ, Ng C, et al. Change in tumor size by RECIST correlates linearly with overall survival in phase I oncology studies. JCO. 2012;30(21):2684-2690. doi: 10.1200/JCO.2011.36.4752
  36. Grimaldi S, Terroir M, Caramella C. Advances in oncological treatment: limitations of RECIST 1.1 criteria. Q J Nucl Med Mol Imaging. 2018;62(2). doi: 10.23736/S1824-4785.17.03038-2
  37. Hodi FS, Ballinger M, Lyons B, et al. Immune-Modified Response Evaluation Criteria In Solid Tumors (imRECIST): Refining Guidelines to Assess the Clinical Benefit of Cancer Immunotherapy. JCO. 2018;36(9):850-858. doi: 10.1200/jco.2017.75.1644
  38. Wolchok J D, Hoos A, O’Day S, et al. Guidelines for the evaluation of immune therapy activity in solid tumors: immune-related response criteria. Clin Cancer Res. 2009;15(23):7412-7420. doi: 10.1158/1078-0432.CCR-09-1624
  39. Zhao B, Schwartz LH, Larson SM. Imaging surrogates of tumor response to therapy: anatomic and functional biomarkers. J Nucl Med. 2009;50(2):239-249. doi: 10.2967/jnumed.108.056655
  40. Choi H, Charnsangavej C, Faria SC, et al. Correlation of computed tomography and positron emission tomography in patients with metastatic gastrointestinal stromal tumor treated at a single institution with imatinib mesylate: proposal of new computed tomography response criteria. JCO. 2007;25(13):1753-1759. doi: 10.1200/JCO.2006.07.3049

41. Tahara M, Ohtsu A, Hironaka S, et al. Clinical Impact of Criteria for Complete Response (CR) of Primary Site to Treatment of Esophageal Cancer. Jpn J Clin Oncol. 2005;35(6):316-323. doi: 10.1093/jjco/hyi095

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