Abstract

There is no consensus on specific prognostic biomarkers potentially improving survival of nasopharyngeal carcinoma (NPC), especially in advanced-stage disease. The prognostic value of MRI-based radiomics signature is unclear. A total of 970 quantitative features were extracted from the tumor of 100 untreated NPC patients (stage III-IVb) (discovery set: n = 70, validation set: n = 30). We then applied least absolute shrinkage and selection operator (lasso) regression to select features that were most associated with progression-free survival (PFS). Candidate prognostic biomarkers included age, gender, overall stage, hemoglobin, platelet counts and radiomics signature. We developed model 1 (without radiomics signature) and model 2 (with radiomics signature) in the discovery set and then tested in the validation set. Multivariable Cox regression analysis was used to yield hazard ratio (HR) of each potential biomarker. We found the radiomics signature stratified patients in the discovery set into a low or high risk group for PFS (HR = 5.14, p < 0.001) and was successfully validated for patients in the validation set (HR = 7.28, p = 0.015). However, the other risk factors showed no significantly prognostic value (all p-values for HR, > 0.05). Accordingly, pretreatment MRI-based radiomics signature is a non-invasive and cost-effective prognostic biomarker in advanced NPC patients, which would improve decision-support in cancer care.

Highlights

  • Nasopharyngeal carcinoma (NPC) is a unique cancer with specific patterns of racial and geographical distribution [1]

  • The results demonstrated that radiomics signature was a significant, independent predictor of progression-free survival (PFS) in the discovery set (HR = 5.14, 95% CI= 4.80-5.48, p < 0.001) and the validation set (HR = 7.28, 95% CI = 6.46-8.09, p = 0.015) (Table 2)

  • Our results reveal that pre-treatment MRI-based radiomics signature is a nonivasive and cost-effective prognostic marker in advanced nasopharyngeal carcinoma (NPC) patients

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Summary

Introduction

Nasopharyngeal carcinoma (NPC) is a unique cancer with specific patterns of racial and geographical distribution [1]. It is especially prevalent in southern China. While concurrent chemoradiotherapy with or without adjuvant chemotherapy has led to gains in overall survival of advanced NPC patients, there is wider recognition that the outcome of these patients are clinically heterogeneous [6]. When they are stratified by clinical stage, differences in long-term survival are evident within the individual stages. There is, a critical need for additional biomarkers for prognostication and precise treatment stratification in advanced NPC patients

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