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TDLN-Guided Lymphadenectomy After Neoadjuvant Immunochemotherapy for ESCC

Tumor-Draining Lymph Node Preservation-Guided Intraoperative Lymphadenectomy After Neoadjuvant Immunochemotherapy for Esophageal Squamous Cell Carcinoma: A Prospective Multicenter Observational Cohort Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07697898
Enrollment
400
Registered
2026-07-13
Start date
2026-07-01
Completion date
2031-06-30
Last updated
2026-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Esophageal Squamous Cell Carcinoma (ESCC)

Brief summary

This is a prospective, multicenter, observational cohort study of patients with esophageal squamous cell carcinoma who have received neoadjuvant immunochemotherapy and are scheduled to undergo curative esophagectomy with standard systematic lymphadenectomy. The study will not alter the current standard surgical approach. All patients will receive curative esophagectomy and systematic lymph node dissection according to institutional practice. Lymph nodes will be separated and recorded by anatomical station during surgery, followed by station-level pathological assessment. Imaging findings, pathological response, perioperative outcomes, recurrence patterns, disease-free survival, overall survival, and selected immune microenvironment features will be collected and analyzed. The purpose of this study is to characterize station-level residual lymph node metastasis risk and immune activity after neoadjuvant immunochemotherapy. The findings may help identify candidate lymph node stations for future research on individualized or lymph node-preserving surgical strategies in esophageal squamous cell carcinoma.

Interventions

PROCEDURECurative Esophagectomy With Systematic Lymphadenectomy

All participants will undergo curative esophagectomy with standard systematic lymphadenectomy according to institutional practice. The study will not intentionally reduce the extent of lymph node dissection. Lymph nodes will be separated, labeled, and recorded by anatomical station for postoperative pathological and exploratory immune microenvironment analyses.

Sponsors

Tongji Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Age 18 to 75 years, regardless of sex. * Eastern Cooperative Oncology Group performance status of 0 to 1. * Histologically confirmed thoracic esophageal squamous cell carcinoma. * Received neoadjuvant immunochemotherapy and considered suitable for curative surgery after multidisciplinary team evaluation. * Clinically resectable locally advanced or locally progressive disease without evidence of distant metastasis. * Completed preoperative contrast-enhanced computed tomography of the neck, chest, and abdomen. Positron emission tomography-computed tomography and/or endoscopic ultrasound may be performed if clinically available. * Considered by the investigator to be able to tolerate curative esophagectomy and standard systematic lymphadenectomy.

Exclusion criteria

* Non-squamous cell carcinoma histology or concurrent primary malignancy requiring treatment. * Previous curative surgery for esophageal cancer or previous radiotherapy for the current esophageal lesion. * Evidence of distant metastasis, unresectable disease, or considered unsuitable for curative surgery after multidisciplinary team evaluation. * Severe autoimmune disease requiring long-term systemic immunosuppressive therapy. * Severe cardiac, pulmonary, hepatic, renal, or other major organ dysfunction that prevents surgery or completion of study-related assessments. * Any other condition that, in the investigator's judgment, makes the participant unsuitable for the study, including poor compliance, inability to complete scheduled follow-up, or inability to provide key study data.

Design outcomes

Primary

MeasureTime frameDescription
2-Year Disease-Free Survival Rate24 months after curative esophagectomyThe proportion of participants who are alive without disease recurrence or distant metastasis at 2 years after curative esophagectomy. Disease-free survival is defined as the time from curative esophagectomy to the first occurrence of local recurrence, regional lymph node recurrence, distant metastasis, or death from any cause. Participants without an event will be censored at the date of last valid follow-up.

Secondary

MeasureTime frameDescription
Overall SurvivalUp to 24 months after curative esophagectomyOverall survival is defined as the time from curative esophagectomy to death from any cause. Participants who are alive will be censored at the date of last follow-up.
2-Year Overall Survival Rate24 months after curative esophagectomyThe proportion of participants who are alive at 2 years after curative esophagectomy.
Locoregional Recurrence RateUp to 24 months after curative esophagectomyThe proportion of participants who develop locoregional recurrence, including recurrence at the primary tumor bed, anastomotic region, or regional lymph nodes.
Distant Metastasis RateUp to 24 months after curative esophagectomyThe proportion of participants who develop distant metastasis, including metastasis to the lung, liver, bone, brain, non-regional lymph nodes, or other distant organs.
Pattern of First FailureUp to 24 months after curative esophagectomyThe site of first recurrence or progression will be classified as local recurrence, regional recurrence, distant metastasis, or mixed recurrence.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 14, 2026