Ultrasound delta-radiomics during radiotherapy to predict recurrence in patients with head and neck squamous cell carcinoma

Clin Transl Radiat Oncol. 2021 Mar 12:28:62-70. doi: 10.1016/j.ctro.2021.03.002. eCollection 2021 May.

Abstract

Purpose: This study investigated the use of quantitative ultrasound (QUS) obtained during radical radiotherapy (RT) as a radiomics biomarker for predicting recurrence in patients with node-positive head-neck squamous cell carcinoma (HNSCC).

Methods: Fifty-one patients with HNSCC were treated with RT (70 Gy/33 fractions) (±concurrent chemotherapy) were included. QUS Data acquisition involved scanning an index neck node with a clinical ultrasound device. Radiofrequency data were collected before starting RT, and after weeks 1, and 4. From this data, 31 spectral and related-texture features were determined for each time and delta (difference) features were computed. Patients were categorized into two groups based on clinical outcomes (recurrence or non-recurrence). Three machine learning classifiers were used for the development of a radiomics model. Features were selected using a forward sequential selection method and validated using leave-one-out cross-validation.

Results: The median follow up for the entire group was 38 months (range 7-64 months). The disease sites involved neck masses in patients with oropharynx (39), larynx (5), carcinoma unknown primary (5), and hypopharynx carcinoma (2). Concurrent chemotherapy and cetuximab were used in 41 and 1 patient(s), respectively. Recurrence was seen in 17 patients. At week 1 of RT, the support vector machine classifier resulted in the best performance, with accuracy and area under the curve (AUC) of 80% and 0.75, respectively. The accuracy and AUC improved to 82% and 0.81, respectively, at week 4 of treatment.

Conclusion: QUS Delta-radiomics can predict higher risk of recurrence with reasonable accuracy in HNSCC.Clinical trial registration: clinicaltrials.gov.in identifier NCT03908684.

Keywords: AAC, Average acoustic concentration; ACE, Attenuation co-efficient estimate; ASD, Average scatterer diameter; AUC, Area under the curve; Acc, Accuracy; CON, Contrast; COR, Correlation; CR, Complete responders; CT, Computed tomography; Delta-radiomics; EBV, Epstein-Barr virus; ENE, Energy; FDG-PET, 18F-fluorodeoxyglucose positron emission tomography; FLD, Fisher’s linear discriminant; FN, False negative; FP, False positive; GLCM, Grey level co-occurrence matrix; HN, Head and neck; HNSCC, Head and neck squamous cell carcinoma; HOM, Homogeneity; HPV, Human papillomavirus; Head and neck malignancy; IGRT, Image-guided radiation therapy; IMRT, Intensity-modulated radiation therapy; MBF, Mid-band fit; MRI, Magnetic resonance imaging; Machine learning; NR, Non-recurrence; PET, Positron emission tomography; PR, Partial responders; QUS, Quantitative ultrasound; Quantitative ultrasound; R, Recurrence; RF, Radiofrequency; RFS, Recurrence-free survival; ROI, Region of interest; RT, Radiotherapy; Radiomics; Radiotherapy squamous cell carcinoma; Recurrence; SAS, Spacing among scatterers; SI, Spectral intercept; SP, Specificity; SS, Spectral slope; SVM, Support vector machine; Sn, Sensitivity; TN, True negative; TP, True positive; US, Ultrasound; kNN, k nearest neighbors.

Associated data

  • ClinicalTrials.gov/NCT03908684