Published online May 15, 2024. doi: 10.4251/wjgo.v16.i5.1849
Peer-review started: December 19, 2023
First decision: January 15, 2024
Revised: January 23, 2024
Accepted: March 4, 2024
Article in press: March 4, 2024
Published online: May 15, 2024
Processing time: 142 Days and 23.5 Hours
Lymph node (LN) staging in rectal cancer (RC) affects treatment decisions and patient prognosis. For radiologists, the traditional preoperative assessment of LN metastasis (LNM) using magnetic resonance imaging (MRI) poses a challenge.
The accuracy of assessing LNM based on MRI remains limited. A meta-analysis demonstrated a sensitivity of approximately 77% and specificity of approximately 71% when using MRI to diagnose metastasis in evaluable LNs. Therefore, there is a risk of diagnostic insufficiency and overdiagnosis.
To explore the value of a nomogram model that combines Conventional MRI and radiomics features from the LNs of RC in assessing the preoperative metastasis of evaluable LNs.
A total of 270 LNs (158 LNM and 112 metastatic) were included and randomly allocated to training set (111 nonmetastatic and 78 metastatic) and validation set (47 nonmetastatic and 34 metastatic) at a 7:3 ratio. Radiomic features were extracted from T1-weighted imaging (T1WI) and T2-weighted imaging (T2WI) images of individual LN. The least absolute shrinkage and selection operator regression analysis was used for feature selection. Multivariate logistic regression analysis was used to develop the Rad-score and nomogram model. Receiver operating characteristic curves were constructed to evaluate the diagnostic performance of the models for predicting LNM. The performance of the nomogram was assessed using decision curve analysis (DCA).
The nomogram model outperformed conventional MRI and single radiomics models in evaluating LNM. In the training set, the nomogram model achieved an area under the curve (AUC) of 0.92, which was significantly higher than the AUCs of 0.82 (P < 0.001) and 0.89 (P < 0.001) of the conventional MRI and radiomics models, respectively. In the validation set, the nomogram model achieved an AUC of 0.91, significantly surpassing 0.80 (P < 0.001) and 0.86 (P < 0.001), respectively.
The nomogram model showed the best performance in predicting metastasis of evaluable LNs.
Radiomics holds great promise for transforming medical practice, especially for patients with RC. However, before its widespread adoption, challenges regarding sample size, model design, and robust multicenter validation sets must be addressed. To validate the proposed model externally, future prospective multicenter studies with larger sample sizes are crucial.