# A nomogram combining clinical variables and MR imaging features for predicting response in head-neck cancer

**Authors:** Xinyan Wang, Yiming Ding, Hangzhi Liu, Changyu Zhu, Xiaoxia Qu, Yue Kang, Cong Ding, Yuchen Wang, Meiling Mao, Zhinxin Li, Xiaohong Chen, Junfang Xian

PMC · DOI: 10.1186/s13244-025-02196-y · Insights into Imaging · 2026-01-27

## TL;DR

This study creates a new model combining clinical data and MRI features to better predict treatment response in head and neck cancer patients.

## Contribution

A novel multimodal nomogram integrating clinical variables and MRI features for predicting neoadjuvant chemoimmunotherapy response in HNSCC.

## Key findings

- A combined model of CPS, tumor diameter, and enhancement pattern achieved an AUC of 0.86 for predicting pCR.
- Enhancement pattern was the strongest MRI predictor of pCR with an AUC of 0.83.
- Functional MRI parameters like Ktrans and ADC had AUCs of 0.712 and 0.715 for pCR prediction.

## Abstract

This study aims to develop a multimodal nomogram to predict neoadjuvant chemoimmunotherapy (NCIT) outcomes in head and neck squamous cell carcinoma (HNSCC).

Treatment-naive HNSCC patients receiving neoadjuvant NCIT were retrospectively analyzed. Clinical information, conventional MR imaging features, dynamic contrast-enhanced-MRI (DCE-MRI) parameters and ADC values were analyzed in relation to pathological complete response (pCR). The predictive accuracy of clinical and MRI parameters was evaluated using the receiver operating characteristic (ROC) curve, with the area under the curve (AUC) serving as a key metric.

Following NCIT, 55.0% (67/122) of patients achieved pCR. Significant differences were observed in clinical variables, including tumor location, combined positive score (CPS) and neutrophil-to-lymphocyte ratio (NLR) between pCR and non-pCR groups (p < 0.05). Imaging features (tumor margin, growth pattern, T2 homogeneity, necrosis, three distinct enhancement patterns, tumor diameter and lymph node short-axis diameter) also differed significantly (p < 0.05). The enhancement pattern was the most efficient predictor of pCR (AUC = 0.83). A combined model incorporating CPS, tumor diameter, and enhancement pattern achieved an AUC of 0.86. The baseline Ktrans and ADC values demonstrated an AUC of 0.712 and 0.715 for pCR prediction. The H&E-stained whole-slide analyses revealed significant correlations between specific MRI features and tumor lymphocyte densities/ratios.

We developed a novel combined model integrating CPS and routine pretreatment MRI features to predict NCIT response in HNSCC. The enhancement pattern was the strongest predictor of pCR, while functional MRI parameters also showed significant predictive value.

This study demonstrates that systematically integrating combined positive score with routine pretreatment MRI features can effectively predict neoadjuvant chemoimmunotherapy response. These findings may help optimize therapeutic strategies for head and neck squamous cell carcinoma.

Predicting neoadjuvant chemoimmunotherapy response in head and neck cancer remains challenging.A novel clinical-MRI model improves chemoimmunotherapy response prediction in head-neck cancer.The three enhancement patterns emerged as the most robust predictors.

Predicting neoadjuvant chemoimmunotherapy response in head and neck cancer remains challenging.

A novel clinical-MRI model improves chemoimmunotherapy response prediction in head-neck cancer.

The three enhancement patterns emerged as the most robust predictors.

## Linked entities

- **Diseases:** head and neck squamous cell carcinoma (MONDO:0010150), head and neck cancer (MONDO:0005627)

## Full-text entities

- **Genes:** CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, AZIN2 (antizyme inhibitor 2) [NCBI Gene 113451] {aka ADC, AZIB1, ODC-p, ODC1L, ODCp}
- **Diseases:** lymph node metastasis (MESH:D008207), hypopharyngeal carcinoma (MESH:D007012), HNSCC (MESH:D000077195), laryngeal cancer (MESH:D007822), squamous cell carcinoma (MESH:D002294), IVb (MESH:D009085), fibrosis (MESH:D005355), cancer (MESH:D009369), hemorrhage (MESH:D006470), head and neck cancer (MESH:D006258), pCR (MESH:D005598), NLR (MESH:D015467), lymph node (MESH:D000072717), necrosis (MESH:D009336), laryngeal and oropharyngeal cancer (MESH:D009959), inflammation (MESH:D007249)
- **Chemicals:** pembrolizumab (MESH:C582435), DCE (-), paclitaxel (MESH:D017239), H&amp;E (MESH:D006371), eosin (MESH:D004801), cisplatin (MESH:D002945), Hematoxylin (MESH:D006416), tislelizumab (MESH:C000707970)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12847587/full.md

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Source: https://tomesphere.com/paper/PMC12847587