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Pathological predictors for lymph node metastasis in T1 colorectal cancer
Hitoshi Yamauchi1, Kazutomo Togashi, Yutaka J Kawamura
1Department of Surgery, Saitama Medical Center, Jichi Medical University, Saitama, Japan.
Surgery Today
|September 30, 2008
Summary
Non-well differentiated tumors and tumor budding are key pathological predictors for lymph node metastasis in early-stage (T1) colorectal cancer, aiding in risk assessment.
Area of Science:
- Oncology
- Pathology
- Gastroenterology
Background:
- T1 colorectal cancer represents early-stage disease.
- Accurate prediction of lymph node metastasis is crucial for treatment planning and prognosis.
- Identifying reliable pathological predictors is essential for risk stratification.
Purpose of the Study:
- To identify pathological predictors for lymph node metastasis in patients with T1 colorectal cancer.
- To evaluate the predictive value of specific pathological features including differentiation, invasion depth, lymphatic/venous invasion, and tumor budding.
Main Methods:
- A retrospective review of 164 patients with single T1 colorectal cancer who underwent surgery.
- Analysis of pathological features: non-well differentiation, invasion depth (>= 2000 microm), lymphatic channel involvement, venous invasion, and tumor budding.
- Logistic regression modeling was used to assess predictor significance for lymph node metastasis.
Main Results:
- Lymph node metastasis was present in 9.8% of patients.
- Non-well differentiation (13.4%) and tumor budding (14.6%) showed higher positive rates.
- Multivariate analysis identified non-well differentiation (P < 0.001) and tumor budding (P = 0.002) as significant predictors.
- A model combining these two factors achieved 94% sensitivity and 82% specificity for predicting lymph node metastasis.
Conclusions:
- Non-well differentiation and tumor budding are significant pathological predictors of lymph node metastasis in T1 colorectal cancer.
- These factors can aid in the accurate risk stratification of patients with early-stage colorectal cancer.
- The findings support the use of these pathological features in clinical decision-making for T1 colorectal cancer management.

