# Impact of gross tumor morphology on the clinical outcomes of colon cancer: multicenter retrospective cohort study

**Authors:** So Jung Han, Hyun Seok Lee, Byung Ik Jang, Jae Hyun Kim, Hyun Gun Kim, Il Hyun Baek, Jun Lee, Bun Kim, Dae Bum Kim, Jae Jun Park

PMC · DOI: 10.1007/s00384-026-05101-1 · 2026-02-04

## TL;DR

This study shows that the visual appearance of colon tumors seen during endoscopy can predict patient survival, especially for stage II colon cancer.

## Contribution

The study demonstrates that gross tumor morphology is an independent prognostic factor in colon cancer.

## Key findings

- Flat/ulceroinfiltrative tumors were linked to worse overall and disease-free survival.
- In stage II patients, morphology had a stronger impact on survival outcomes.
- Gross morphology was confirmed as an independent predictor of poor survival.

## Abstract

While histopathological features are established prognostic factors in colorectal cancer, the prognostic significance of gross tumor morphology remains unclear. We investigated whether endoscopic gross morphology is associated with clinical outcomes in colon cancer.

We performed a multicenter retrospective analysis of 1,177 patients with colon cancer who underwent curative-intent endoscopic or surgical resection between 2010 and 2019. Tumors were categorized based on endoscopic images as flat/ulceroinfiltrative (n = 345) or fungating/ulcerofungating (n = 832). Kaplan–Meier analysis assessed survival outcomes, and Cox proportional hazards models identified independent prognostic factors, adjusting for age, sex, family history, diabetes, CEA, and AJCC 7th edition stage.

Patients with flat/ulceroinfiltrative tumors had significantly shorter overall survival (OS, p = 0.001) and disease-free survival (DFS, p = 0.024) than those with fungating/ulcerofungating tumors. In stage II patients, the difference in OS by morphology was more pronounced (p = 0.004). Multivariate analysis confirmed flat/ulceroinfiltrative morphology as an independent predictor of poor OS (HR 1.61; 95% CI 1.122–2.335; p = 0.010). Other significant predictors included older age (≥ 65 years, HR 1.533; p = 0.021), poor histologic grade (PD vs. WD/MD, HR 5.308; p < 0.001), and advanced stage.

Gross endoscopic morphology is an independent prognostic factor in colon cancer. Flat/ulceroinfiltrative tumors are associated with worse outcomes, especially in stage II disease. Gross morphology, readily identifiable at diagnosis, may aid risk stratification and inform decisions regarding adjuvant therapy.

The online version contains supplementary material available at 10.1007/s00384-026-05101-1.

## Linked entities

- **Diseases:** colon cancer (MONDO:0002032)

## Full-text entities

- **Genes:** KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845] {aka 'C-K-RAS, C-K-RAS, CFC2, K-RAS2A, K-RAS2B, K-RAS4A}, RBBP4 (RB binding protein 4, chromatin remodeling factor) [NCBI Gene 5928] {aka NURF55, RBAP48, lin-53}, TENM1 (teneurin transmembrane protein 1) [NCBI Gene 10178] {aka ODZ1, ODZ3, TEN-M1, TEN1, TNM, TNM1}, BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}
- **Diseases:** Colorectal cancer (MESH:D015179), Stage II disease (MESH:D007676), epithelial tumors (MESH:D002277), carcinogenesis (MESH:D063646), Gastrointestinal Cancer (MESH:D005770), PD (MESH:D010300), diabetes (MESH:D003920), depressed (MESH:D003866), metastases (MESH:D009362), MD (MESH:C535955), death (MESH:D003643), II disease (MESH:D004194), gastrointestinal stromal tumors (MESH:D046152), peritoneal dissemination (MESH:D010538), LSTs (MESH:D009369), gastric cancer (MESH:D013274), lymphoma (MESH:D008223), lymph node metastasis (MESH:D008207), colon adenocarcinoma (MESH:D003110), WD (MESH:D006527), oncologic (MESH:D000072716), microsatellite (MESH:D053842), Borrmann type IV (MESH:C000631847), hypertension (MESH:D006973)
- **Chemicals:** alcohol (MESH:D000438), Flat (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12872715/full.md

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Source: https://tomesphere.com/paper/PMC12872715