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May 6, 2026International Journal of Surgery0 citationsOpen Access

Noninvasive identification of nasopharyngeal lesions by MRI-based radiomic-clinical model: a multicenter study

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LWLiuling WangXFXiaobin FuXLXiyi Liao

Key Points

  • This research aims to develop and assess MRI-based radiomic-clinical models for identifying nasopharyngeal lesions.
  • Multicenter retrospective study involving 350 patients.
  • MRI sequences including T1-weighted, T2-weighted, and contrast-enhanced T1-weighted images were analyzed.
  • Altruistic seagull optimization algorithm (AltSOA) combined with a support vector machine classifier was employed for feature selection.
  • Radiomic models achieved large areas under the curve (AUC), but limited performance on other metrics.
  • Radiomic-clinical models resulted in improved precision and F1-scores with comparable AUCs.
  • The T1WI + CE-T1WI radiomic-clinical model had the best performance with AUC = 0.909 in internal testing.

Abstract

Background: Nasopharyngeal lesions encompass a broad spectrum of benign and malignant diseases with overlapping imaging features, posing diagnostic challenges. Early and accurate identification is essential to guide appropriate management and avoid unnecessary invasive procedures. In this study, radiomic-clinical diagnostic models for the identification of five nasopharyngeal lesion types via the altruistic seagull optimization algorithm (AltSOA) were developed and evaluated. Materials and methods: In total, 350 patients from three medical centers were retrospectively included. Radiomics features were extracted from magnetic resonance imaging (MRI) sequences T1-weighted images (T1WI), T2-weighted images, and contrast-enhanced (CE)-T1WI. The AltSOA with an embedded support vector machine classifier was used for feature selection. Diagnostic models (radiomic and radiomic-clinical) were constructed based on combinations of multimodal MRI sequences. Results: The radiomic models achieved large areas under the curve (AUCs) but limited performance according to other metrics. The radiomic-clinical models yielded comparable AUCs and improved precision and recall values and F1-scores. The T1WI + CE-T1WI radiomic-clinical model achieved the best performance (internal testing set: AUC = 0.909 95% CI, 0.868–0.951; external testing set: AUC = 0.825 95% CI, 0.736–0.900). SHAP analysis revealed the main contributing features, and the directions and magnitudes of their impacts on the predicted diagnostic classification. Conclusion: These findings potentially reduce unnecessary biopsy performance and advance personalized medicine.

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Cite This Study

Wang et al. (2026) studied this question.

synapsesocial.com/papers/69fa980604f884e66b531e23https://doi.org/10.1097/js9.0000000000005288
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