Quantifying tumour heterogeneity in 18F-FDG PET/CT imaging by texture analysis

被引:373
作者
Chicklore, Sugama [1 ]
Goh, Vicky [1 ]
Siddique, Musib [1 ]
Roy, Arunabha [1 ]
Marsden, Paul K. [1 ]
Cook, Gary J. R. [1 ]
机构
[1] Kings Coll London, St Thomas Hosp, Clin PET Ctr, Div Imaging Sci & Biomed Engn, London SE1 7EH, England
基金
英国工程与自然科学研究理事会;
关键词
(18)FDG PET/CT; Texture analysis; Radiomics; Heterogeneity; CELL LUNG-CANCER; POSITRON-EMISSION-TOMOGRAPHY; FDG-PET; SPATIAL HETEROGENEITY; COMPUTED-TOMOGRAPHY; RESPONSE EVALUATION; FRACTAL ANALYSIS; PROGNOSTIC VALUE; MRI; IMAGES;
D O I
10.1007/s00259-012-2247-0
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
F-18-Fluorodeoxyglucose positron emission tomography/computed tomography (F-18-FDG PET/CT) is now routinely used in oncological imaging for diagnosis and staging and increasingly to determine early response to treatment, often employing semiquantitative measures of lesion activity such as the standardized uptake value (SUV). However, the ability to predict the behaviour of a tumour in terms of future therapy response or prognosis using SUVs from a baseline scan prior to treatment is limited. It is recognized that medical images contain more useful information than may be perceived with the naked eye, leading to the field of "radiomics" whereby additional features can be extracted by computational postprocessing techniques. In recent years, evidence has slowly accumulated showing that parameters obtained by texture analysis of radiological images, reflecting the underlying spatial variation and heterogeneity of voxel intensities within a tumour, may yield additional predictive and prognostic information. It is hoped that measurement of these textural features may allow better tissue characterization as well as better stratification of treatment in clinical trials, or individualization of future cancer treatment in the clinic, than is possible with current imaging biomarkers. In this review we focus on the literature describing the emerging methods of texture analysis in (18)FDG PET/CT, as well as other imaging modalities, and how the measurement of spatial variation of voxel grey-scale intensity within an image may provide additional predictive and prognostic information, and postulate the underlying biological mechanisms.
引用
收藏
页码:133 / 140
页数:8
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