The Influence of the Exclusion of Central Necrosis on [18F]FDG PET Radiomic Analysis

被引:9
作者
Noortman, Wyanne A. [1 ,2 ]
Vriens, Dennis [1 ]
Mooij, Charlotte D. Y. [1 ,3 ]
Slump, Cornelis H. [2 ]
Aarntzen, Erik H. [4 ]
van Berkel, Anouk [5 ]
Timmers, Henri J. L. M. [5 ]
Bussink, Johan [6 ]
Meijer, Tineke W. H. [7 ]
de Geus-Oei, Lioe-Fee [1 ,2 ]
van Velden, Floris H. P. [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Radiol, Sect Nucl Med, NL-2333 ZA Leiden, Netherlands
[2] TechMed Ctr, NL-7522 NB Enschede, Netherlands
[3] Delft Univ Technol, Tech Med, NL-2628 CD Delft, Netherlands
[4] Radboud Univ Nijmegen, Med Ctr, Dept Radiol & Nucl Med, NL-6525 GA Nijmegen, Netherlands
[5] Radboud Univ Nijmegen, Med Ctr, Dept Internal Med, Div Endocrinol, NL-6525 GA Nijmegen, Netherlands
[6] Radboud Univ Nijmegen, Med Ctr, Radiotherapy & OncoImmunol Lab, Dept Radiat Oncol, NL-6525 GA Nijmegen, Netherlands
[7] Univ Med Ctr Groningen, Dept Radiat Oncol, NL-9713 GZ Groningen, Netherlands
关键词
radiomics; F-18]FDG PET/CT; tumour delineation; central necrosis; CELL LUNG-CANCER; TUMOR DELINEATION; F-18-FDG PET; REPEATABILITY; HETEROGENEITY; FEATURES; VOLUME;
D O I
10.3390/diagnostics11071296
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Central necrosis can be detected on [F-18]FDG PET/CT as a region with little to no tracer uptake. Currently, there is no consensus regarding the inclusion of regions of central necrosis during volume of interest (VOI) delineation for radiomic analysis. The aim of this study was to assess how central necrosis affects radiomic analysis in PET. Methods: Forty-three patients, either with non-small cell lung carcinomas (NSCLC, n = 12) or with pheochromocytomas or paragangliomas (PPGL, n = 31), were included retrospectively. VOIs were delineated with and without central necrosis. From all VOIs, 105 radiomic features were extracted. Differences in radiomic features between delineation methods were assessed using a paired t-test with Benjamini-Hochberg multiple testing correction. In the PPGL cohort, performances of the radiomic models to predict the noradrenergic biochemical profile were assessed by comparing the areas under the receiver operating characteristic curve (AUC) for both delineation methods. Results: At least 65% of the features showed significant differences between VOIvital-tumour and VOIgross-tumour (65%, 79% and 82% for the NSCLC, PPGL and combined cohort, respectively). The AUCs of the radiomic models were not significantly different between delineation methods. Conclusion: In both tumour types, almost two-third of the features were affected, demonstrating that the impact of whether or not to include central necrosis in the VOI on the radiomic feature values is significant. Nevertheless, predictive performances of both delineation methods were comparable. We recommend that radiomic studies should report whether or not central necrosis was included during delineation.
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页数:13
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