Population-based analysis on predictors for lymph node metastasis in T1 colon cancer
Aged, 80 and over
Male
Incidence
Middle Aged
Prognosis
Adenocarcinoma, Mucinous
Survival Analysis
Article
3. Good health
03 medical and health sciences
Logistic Models
0302 clinical medicine
Risk Factors
Lymphatic Metastasis
Colonic Neoplasms
Odds Ratio
Humans
Female
Aged
Neoplasm Staging
Proportional Hazards Models
Retrospective Studies
DOI:
10.1007/s00464-019-07192-0
Publication Date:
2019-10-16T12:18:47Z
AUTHORS (7)
ABSTRACT
Abstract
Background
In this study, we aimed to identify independent predictive factors for lymph node metastasis (LNM) in T1 colon cancer.
Methods
Data of 8056 eligible patients were retrospectively collected from the Surveillance, Epidemiology, and End Results (SEER) database during 2004–2012. We performed logistic regression analysis to identify predictive factors for LNM. Both unadjusted and adjusted Cox regression analyses were used to determine the association between LNM and patient survival. Finally, we used competing risks analysis and the cumulative incidence function (CIF) to further confirm the prognostic role of LNM in cancer-specific survival (CSS).
Results
The overall risk of LNM in patients with T1 colon cancer was 12.0% (N = 967). Adjusted logistic regression models revealed that mucinous carcinoma [odds ratio (OR) = 2.26, P < 0.001], moderately differentiated (OR 1.74, P < 0.001), poorly differentiated (OR 5.16, P < 0.001), and undifferentiated carcinoma (OR 3.01, P = 0.003); older age (OR 0.66, P < 0.001 for age 65–79 years, OR 0.44, P < 0.001 for age over 80 years); and carcinoma located in the ascending colon (OR 0.77, P = 0.018) and sigmoid colon (OR 1.24, P = 0.014) were independent predictive factors for LNM. Adjusted Cox regression analysis showed that positive lymph node involvement was significantly associated with CSS [hazard ratio (HR) = 3.02, P < 0.001], which was further robustly confirmed using a competing risks model and the CIF.
Conclusions
This population-based study showed that mucinous carcinoma, tumor grade, age, and primary tumor location were independent predictive factors for LNM in T1 colon cancer. The risk of LNM should be carefully evaluated in patients with T1 colon cancer, before clinical management.
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