Auto-segmentation of neck nodal metastases using self-distilled masked image transformer on longitudinal MR images

Author:

Paudyal Ramesh1ORCID,Jiang Jue1,Han James2,Diplas Bill H2,Riaz Nadeem2ORCID,Hatzoglou Vaios3,Lee Nancy2,Deasy Joseph O1ORCID,Veeraraghavan Harini1,Shukla-Dave Amita13ORCID

Affiliation:

1. Department of Medical Physics, Memorial Sloan Kettering Cancer Center , New York, NY 10065, United States

2. Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center , New York, NY 10065, United States

3. Department of Radiology, Memorial Sloan Kettering Cancer Center , New York, NY 10065, United States

Abstract

Abstract Objectives Auto-segmentation promises greater speed and lower inter-reader variability than manual segmentations in radiation oncology clinical practice. This study aims to implement and evaluate the accuracy of the auto-segmentation algorithm, “Masked Image modeling using the vision Transformers (SMIT),” for neck nodal metastases on longitudinal T2-weighted (T2w) MR images in oropharyngeal squamous cell carcinoma (OPSCC) patients. Methods This prospective clinical trial study included 123 human papillomaviruses (HPV-positive [+]) related OSPCC patients who received concurrent chemoradiotherapy. T2w MR images were acquired on 3 T at pre-treatment (Tx), week 0, and intra-Tx weeks (1-3). Manual delineations of metastatic neck nodes from 123 OPSCC patients were used for the SMIT auto-segmentation, and total tumor volumes were calculated. Standard statistical analyses compared contour volumes from SMIT vs manual segmentation (Wilcoxon signed-rank test [WSRT]), and Spearman’s rank correlation coefficients (ρ) were computed. Segmentation accuracy was evaluated on the test data set using the dice similarity coefficient (DSC) metric value. P-values <0.05 were considered significant. Results No significant difference in manual and SMIT delineated tumor volume at pre-Tx (8.68 ± 7.15 vs 8.38 ± 7.01 cm3, P = 0.26 [WSRT]), and the Bland-Altman method established the limits of agreement as –1.71 to 2.31 cm3, with a mean difference of 0.30 cm3. SMIT model and manually delineated tumor volume estimates were highly correlated (ρ = 0.84-0.96, P < 0.001). The mean DSC metric values were 0.86, 0.85, 0.77, and 0.79 at the pre-Tx and intra-Tx weeks (1-3), respectively. Conclusions The SMIT algorithm provides sufficient segmentation accuracy for oncological applications in HPV+ OPSCC. Advances in knowledge First evaluation of auto-segmentation with SMIT using longitudinal T2w MRI in HPV+ OPSCC.

Funder

NIH

NCI Cancer Center

Publisher

Oxford University Press (OUP)

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