TY - GEN
T1 - Robust radiomic feature selection in digital mammography
T2 - Medical Imaging 2020: Computer-Aided Diagnosis
AU - Acciavatti, Raymond J.
AU - Cohen, Eric A.
AU - Maghsoudi, Omid Haji
AU - Gastounioti, Aimilia
AU - Pantalone, Lauren
AU - Hsieh, Meng Kang
AU - Conant, Emily F.
AU - Scott, Christopher G.
AU - Winham, Stacey J.
AU - Kerlikowske, Karla
AU - Vachon, Celine
AU - Maidment, Andrew D.A.
AU - Kontos, Despina
N1 - Publisher Copyright:
© 2020 SPIE.
PY - 2020
Y1 - 2020
N2 - Studies have shown that combining calculations of radiomic features with estimates of mammographic density results in an even better assessment of breast cancer risk than density alone. However, to ensure that risk assessment calculations are consistent across different imaging acquisition settings, it is important to identify features that are not overly sensitive to changes in these settings. In this study, digital mammography (DM) images of an anthropomorphic phantom ("Rachel", Gammex 169, Madison, WI) were acquired at various technique settings. We varied kV and mAs, which control contrast and noise, respectively. DM images in women with negative screening exams were also analyzed. Radiomic features were calculated in the raw ("FOR PROCESSING") DM images; i.e., grey-level histogram, co-occurrence, run length, fractal dimension, Gabor Wavelet, local binary pattern, Laws, and co-occurrence Laws features. For each feature, the range of variation across technique settings in phantom images was calculated. This range was scaled against the range of variation in the clinical distribution (specifically, the range corresponding to the middle 90% of the distribution). In order for a radiomic feature to be considered robust, this metric of imaging acquisition variation (IAV) should be as small as possible (approaching zero). An IAV threshold of 0.25 was proposed for the purpose of this study. Out of 341 features, 284 features (83%) met the threshold IAV ≤ 0.25. In conclusion, we have developed a method to identify robust radiomic features in DM.
AB - Studies have shown that combining calculations of radiomic features with estimates of mammographic density results in an even better assessment of breast cancer risk than density alone. However, to ensure that risk assessment calculations are consistent across different imaging acquisition settings, it is important to identify features that are not overly sensitive to changes in these settings. In this study, digital mammography (DM) images of an anthropomorphic phantom ("Rachel", Gammex 169, Madison, WI) were acquired at various technique settings. We varied kV and mAs, which control contrast and noise, respectively. DM images in women with negative screening exams were also analyzed. Radiomic features were calculated in the raw ("FOR PROCESSING") DM images; i.e., grey-level histogram, co-occurrence, run length, fractal dimension, Gabor Wavelet, local binary pattern, Laws, and co-occurrence Laws features. For each feature, the range of variation across technique settings in phantom images was calculated. This range was scaled against the range of variation in the clinical distribution (specifically, the range corresponding to the middle 90% of the distribution). In order for a radiomic feature to be considered robust, this metric of imaging acquisition variation (IAV) should be as small as possible (approaching zero). An IAV threshold of 0.25 was proposed for the purpose of this study. Out of 341 features, 284 features (83%) met the threshold IAV ≤ 0.25. In conclusion, we have developed a method to identify robust radiomic features in DM.
KW - anthropomorphic phantom
KW - breast cancer.
KW - digital mammography
KW - radiomics
KW - risk assessment
KW - robustness
UR - http://www.scopus.com/inward/record.url?scp=85085512887&partnerID=8YFLogxK
U2 - 10.1117/12.2549163
DO - 10.1117/12.2549163
M3 - Conference contribution
AN - SCOPUS:85085512887
T3 - Progress in Biomedical Optics and Imaging - Proceedings of SPIE
BT - Medical Imaging 2020
A2 - Hahn, Horst K.
A2 - Mazurowski, Maciej A.
PB - SPIE
Y2 - 16 February 2020 through 19 February 2020
ER -