Evidence map›Paper›PMID 42753062›Full record

ArticleAnnals of surgical oncology2026

Prognostic Impact of Bulky Lymph Node Metastasis in Thoracic Esophageal Squamous Cell Carcinoma: A Multicenter Cohort Study.

Guoqing Zhang, Kanghua Zhang, Chang Yuan, Yan Zhang, Teng Mu, Jia Jiao, Long Qiu, Xue Pan, Jia Zhao, Zhigang Li and 1 more

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Article in Annals of surgical oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Guoqing Zhang *State Key Laboratory of Metabolic Dysregulation and Prevention and Treatment of Esophageal Cancer, Zhengzhou, Henan Province, China.
Kanghua Zhang *State Key Laboratory of Metabolic Dysregulation and Prevention and Treatment of Esophageal Cancer, Zhengzhou, Henan Province, China.
Chang YuanState Key Laboratory of Metabolic Dysregulation and Prevention and Treatment of Esophageal Cancer, Department of Thoracic Surgery, Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Yan ZhangState Key Laboratory of Metabolic Dysregulation and Prevention and Treatment of Esophageal Cancer, Zhengzhou, Henan Province, China.
Teng MuState Key Laboratory of Metabolic Dysregulation and Prevention and Treatment of Esophageal Cancer, Zhengzhou, Henan Province, China.
Jia JiaoState Key Laboratory of Metabolic Dysregulation and Prevention and Treatment of Esophageal Cancer, Zhengzhou, Henan Province, China.
Long QiuState Key Laboratory of Metabolic Dysregulation and Prevention and Treatment of Esophageal Cancer, Zhengzhou, Henan Province, China.
Xue PanState Key Laboratory of Metabolic Dysregulation and Prevention and Treatment of Esophageal Cancer, Zhengzhou, Henan Province, China.
Jia ZhaoState Key Laboratory of Metabolic Dysregulation and Prevention and Treatment of Esophageal Cancer, Zhengzhou, Henan Province, China. fcczhaoj2@zzu.edu.cn.
Zhigang LiState Key Laboratory of Metabolic Dysregulation and Prevention and Treatment of Esophageal Cancer, Department of Thoracic Surgery, Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. zhigang.li@shsmu.edu.cn.
Xiangnan LiState Key Laboratory of Metabolic Dysregulation and Prevention and Treatment of Esophageal Cancer, Zhengzhou, Henan Province, China. lxn-2000@163.com.

Funding

Fund of China Medical and Health Cause Development Foundation No. K20250242Key Scientific Research Project of Institutions of Higher Education in Henan Province No. 26A320031the Science and Technology Bureau basic research and applied basic research of Zhengzhou No. 2024ZZJCYJ043the State Key Laboratory of Metabolic Dysregulation & Prevention and Treatment of Esophageal Cancer No. 2025SGAQZ-ZDB-06
6 · The paper itself

Abstract

backgroundThe prognostic relevance of bulky lymph node metastases in esophageal squamous cell carcinoma (ESCC) after neoadjuvant immunochemotherapy remains uncertain.

methodsThis multicenter retrospective cohort included 1247 patients with thoracic ESCC receiving PD-1 inhibitor-based immunochemotherapy followed by R0 esophagectomy at three Chinese centers during 2020-2025. Bulky nodal disease was defined as a radiologically suspected metastatic lymph node with maximum axial diameter ≥ 20 mm. Pathologic response, nodal downstaging, recurrence, postoperative morbidity, overall survival (OS), and disease-free survival (DFS) were compared. Cox models evaluated prognostic association and incremental value beyond cTNM staging.

resultsBulky nodal disease occurred in 218 patients (17.5%) and was associated with more advanced cT, cN, and cM categories. Pathologic complete response (pCR) (19.3% vs. 21.1%; P = .55) and major pathologic response (48.2% vs. 43.5%; P = .21) rates were comparable. Among cN-positive patients, nodal downstaging was less frequent with bulky disease (40.8% vs. 57.1%; P < .001), with more residual positive lymph nodes (2.5 vs. 1.1; P < .001). Two-year OS was 71.9% versus 77.6% (P = .03), and DFS was 64.3% vs. 73.4% (P = .003). Distant recurrence was more frequent (9.6% vs. 4.7%; P = .004). After additional adjustment for cT, cN, and cM, bulky status was no longer significantly associated with DFS or OS and did not improve model fit. Among patients achieving pCR, survival and recurrence did not differ by bulky status.

conclusionsBulky nodal disease marks an imaging-defined high-risk ESCC phenotype characterized by poorer nodal response and observed survival, but its incremental prognostic value beyond cTNM staging appears limited. Pathologic complete response attenuated its adverse prognostic association.

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PMID42753062

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