# Risk factors and a predictive nomogram for regional lymph node metastasis in deficient mismatch repair colorectal cancer

**Authors:** Jiawei He, Tao Wu, Maofa Gao, Yunfeng Jiao, Qiaoling Yu, Yaling Zhao, Ni Hou, Jie Li

PMC · DOI: 10.3389/fonc.2025.1601993 · Frontiers in Oncology · 2025-06-19

## TL;DR

This study identifies risk factors for lymph node metastasis in a specific type of colorectal cancer and creates a tool to predict it before surgery.

## Contribution

The paper introduces a new predictive nomogram for regional lymph node metastasis in dMMR colorectal cancer patients.

## Key findings

- Age, tumor location, differentiation, invasion depth, and MMR protein staining were identified as independent risk factors for lymph node metastasis.
- The developed nomogram showed good discriminability and calibration for predicting metastasis preoperatively.
- Decision curve analysis confirmed the nomogram's clinical utility for early prediction of regional lymph node metastasis.

## Abstract

The present study aims to investigate the risk factors associated with regional lymph node metastasis (LNM) in patients with deficient mismatch repair (dMMR) colorectal cancer (CRC) and develop a nomogram for predicting it preoperatively.

Clinicopathological data of patients who underwent surgical treatment at the Second Affiliated Hospital of Xi’an Jiaotong University between January 2021 and December 2024 were collected, and univariate and multivariate logistic regression analyses were performed to identify the independent risk factors for regional LNM. A clinicopathologic nomogram for preoperatively predicting LNM was established and further validated and evaluated.

A total of 131 patients with stage I to III dMMR/microsatellite instability (MSI) CRC were included in the study. The results showed that age, tumor location, degree of differentiation, depth of invasion, and negative immunohistochemistry staining results for MMR proteins, except for the double-negative of MLH1 and PMS2 or MSH2 and MSH6, were independent risk factors for regional LNM in dMMR/MSI CRC. They were incorporated into the individualized prediction nomogram, which showed sufficient discriminability and good calibration. Decision curve analysis indicated that the nomogram could be used for early clinical prediction of regional LNM.

The clinicopathological nomogram, incorporating five independent risk factors, can be widely used to facilitate the preoperative prediction of regional LNM in patients with dMMR/MSI colorectal cancer, thereby developing individual treatment and improving patients’ prognoses. While the model was internally validated, further external validation is also warranted.

## Linked entities

- **Proteins:** MLH1 (mutL homolog 1), PMS2 (PMS1 homolog 2, mismatch repair system component), MSH2 (mutS homolog 2), MSH6 (mutS homolog 6)
- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** PMS2 (PMS1 homolog 2, mismatch repair system component) [NCBI Gene 5395] {aka HNPCC4, LYNCH4, MLH4, MMRCS4, PMS-2, PMSL2}, MLH1 (mutL homolog 1) [NCBI Gene 4292] {aka COCA2, FCC2, HNPCC, HNPCC2, LYNCH2, MLH-1}, MSH2 (mutS homolog 2) [NCBI Gene 4436] {aka COCA1, FCC1, HNPCC, HNPCC1, LCFS2, LYNCH1}, MSH6 (mutS homolog 6) [NCBI Gene 2956] {aka GTBP, GTMBP, HNPCC5, HSAP, LYNCH5, MMRCS3}
- **Diseases:** CRC (MESH:D015179), tumor (MESH:D009369), LNM (MESH:D008207), deficient (MESH:D007153), MSI (MESH:C536928), microsatellite instability (MESH:D053842)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12221919/full.md

## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12221919/full.md

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Source: https://tomesphere.com/paper/PMC12221919