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Site-Specific Variation in Radiomic Features of Head and Neck Squamous Cell Carcinoma and Its Impact on Machine Learning Models.

Authors :
Liu X
Maleki F
Muthukrishnan N
Ovens K
Huang SH
Pérez-Lara A
Romero-Sanchez G
Bhatnagar SR
Chatterjee A
Pusztaszeri MP
Spatz A
Batist G
Payabvash S
Haider SP
Mahajan A
Reinhold C
Forghani B
O'Sullivan B
Yu E
Forghani R
Source :
Cancers [Cancers (Basel)] 2021 Jul 24; Vol. 13 (15). Date of Electronic Publication: 2021 Jul 24.
Publication Year :
2021

Abstract

Current radiomic studies of head and neck squamous cell carcinomas (HNSCC) are typically based on datasets combining tumors from different locations, assuming that the radiomic features are similar based on histopathologic characteristics. However, molecular pathogenesis and treatment in HNSCC substantially vary across different tumor sites. It is not known if a statistical difference exists between radiomic features from different tumor sites and how they affect machine learning model performance in endpoint prediction. To answer these questions, we extracted radiomic features from contrast-enhanced neck computed tomography scans (CTs) of 605 patients with HNSCC originating from the oral cavity, oropharynx, and hypopharynx/larynx. The difference in radiomic features of tumors from these sites was assessed using statistical analyses and Random Forest classifiers on the radiomic features with 10-fold cross-validation to predict tumor sites, nodal metastasis, and HPV status. We found statistically significant differences ( p -value ≤ 0.05) between the radiomic features of HNSCC depending on tumor location. We also observed that differences in quantitative features among HNSCC from different locations impact the performance of machine learning models. This suggests that radiomic features may reveal biologic heterogeneity complementary to current gold standard histopathologic evaluation. We recommend considering tumor site in radiomic studies of HNSCC.

Details

Language :
English
ISSN :
2072-6694
Volume :
13
Issue :
15
Database :
MEDLINE
Journal :
Cancers
Publication Type :
Academic Journal
Accession number :
34359623
Full Text :
https://doi.org/10.3390/cancers13153723