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Nasopharyngeal carcinoma (NPC), a head and neck malignancy, is highly sensitive to radiation. Accordingly, radiotherapy has long been the primary curative modality for patients with non-metastatic NPC. Although intensity-modulated radiotherapy has significantly improved target conformality and normal tissue protection, local recurrence, distant metastasis, and late toxicity remain important issues in long-term management. To achieve a balance between tumor control and normal tissue protection, the continuous integration of multi-source information throughout the treatment workflow is critical. Radiomics has the potential to quantify spatial heterogeneity that may not be fully captured by conventional visual assessment. In this review, radiomics-driven multimodal integration refers to the task-specific combination of imaging-derived phenotypes with complementary clinical variables, Epstein–Barr virus DNA (EBV-DNA), hematological biomarkers, dose distributions, pathological features, molecular data, longitudinal imaging, or treatment-delivery information for defined radiotherapy decisions. This review focuses on the clinical timeline of precision radiotherapy for NPC and provides an overview of radiomics-driven multimodal integration studies. It discusses the current applications and limitations of this framework in pretreatment risk stratification and treatment selection, target volume and organ-at-risk definition during radiotherapy planning, on-treatment monitoring and adaptive radiotherapy, toxicity prediction and normal-tissue protection, and post-treatment recurrence assessment and re-irradiation decision-making. This synthesis of current evidence, clinical barriers, and methodological considerations may inform future validation and implementation of radiomics-driven multimodal integration in NPC precision radiotherapy.
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Ma et al. (2026) studied this question.
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