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Reproducibility of radiomics for deciphering tumor phenotype with imaging

Binsheng ZhaoDepartment of Radiology, Columbia University Medical Center, 710 West 168th Street, New York NY 10032, USAYongqiang TanDepartment of Radiology, Columbia University Medical Center, 710 West 168th Street, New York NY 10032, USAWei‐Yann TsaiDepartment of Biostatistics, Columbia University Medical Center, 722 West 168th Street, New York NY 10032, USAJing QiDepartment of Radiology, Columbia University Medical Center, 710 West 168th Street, New York NY 10032, USAChuanmiao XieDepartment of Radiology, Columbia University Medical Center, 710 West 168th Street, New York NY 10032, USALin LüDepartment of Radiology, Columbia University Medical Center, 710 West 168th Street, New York NY 10032, USALawrence H. SchwartzDepartment of Radiology, Columbia University Medical Center, 710 West 168th Street, New York NY 10032, USA
2016en
ABI

Аннотация

Radiomics (radiogenomics) characterizes tumor phenotypes based on quantitative image features derived from routine radiologic imaging to improve cancer diagnosis, prognosis, prediction and response to therapy. Although radiomic features must be reproducible to qualify as biomarkers for clinical care, little is known about how routine imaging acquisition techniques/parameters affect reproducibility. To begin to fill this knowledge gap, we assessed the reproducibility of a comprehensive, commonly-used set of radiomic features using a unique, same-day repeat computed tomography data set from lung cancer patients. Each scan was reconstructed at 6 imaging settings, varying slice thicknesses (1.25 mm, 2.5 mm and 5 mm) and reconstruction algorithms (sharp, smooth). Reproducibility was assessed using the repeat scans reconstructed at identical imaging setting (6 settings in total). In separate analyses, we explored differences in radiomic features due to different imaging parameters by assessing the agreement of these radiomic features extracted from the repeat scans reconstructed at the same slice thickness but different algorithms (3 settings in total). Our data suggest that radiomic features are reproducible over a wide range of imaging settings. However, smooth and sharp reconstruction algorithms should not be used interchangeably. These findings will raise awareness of the importance of properly setting imaging acquisition parameters in radiomics/radiogenomics research.

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