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Published on: February 10, 2017
Dynamic Changes in Inflammatory Cytokines and T-Lymphocyte Subsets after Endoscopic Submucosal Dissection for Early
Lei Huang1, Peilong Wang2, Zhibin Bi3
1Department of Gastroenterology, Heji Hospital Affiliated to Changzhi Medical College, Changzhi, Shanxi Province, China. Lhuang06052@163.com.
Journal of Gastrointestinal and Liver Diseases : JGLD
|June 28, 2026
Summary
Endoscopic submucosal dissection (ESD) improves immune markers in early gastrointestinal cancer. Curative resection offers the best outcomes and lowest complication rates.
Area of Science:
- Gastroenterology
- Oncology
- Immunology
Background:
- Early gastrointestinal cancers require effective treatment.
- Endoscopic submucosal dissection (ESD) is a minimally invasive endoscopic procedure for resecting early gastrointestinal neoplasms.
- Understanding the impact of ESD on immune status is crucial for patient recovery.
Purpose of the Study:
- To characterize dynamic changes in inflammation and T-lymphocyte subsets after ESD in early gastrointestinal cancer.
- To correlate these changes with resection quality and clinical factors.
- To compare outcomes across different tumor sites and resection groups.
Main Methods:
- 189 patients with early esophageal, gastric, or colorectal cancer undergoing ESD were analyzed.
- Patients were grouped by resection quality: non-R0 en bloc, non-curative R0, and curative R0.
- T-lymphocyte subsets, inflammatory markers, and complications were assessed pre- and post-ESD.
Main Results:
- ESD significantly improved T-lymphocyte subsets and inflammatory cytokines, especially in the curative resection group.
- Marker levels correlated with lesion size, tumor morphology, and invasion depth.
- Curative resection had the lowest complication rate; non-R0 resection had the highest.
Conclusions:
- ESD effectively ameliorates immune dysregulation in early gastrointestinal cancer.
- Resection quality is a key factor influencing therapeutic benefit and complications.
- Immune improvements post-ESD were consistent across different GI cancer sites.
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