4.3 Article

The effect of post-injection 18F-FDG PET scanning time on texture analysis of peripheral nerve sheath tumours in neurofibromatosis-1

期刊

EJNMMI RESEARCH
卷 7, 期 -, 页码 -

出版社

SPRINGEROPEN
DOI: 10.1186/s13550-017-0282-3

关键词

Texture features; Neurofibromatosis-1; F-18-FDG PET/CT

资金

  1. National Institute for Health Research Biomedical Research Centre of Guys
  2. St Thomas' NHS Trust in partnership
  3. King's College London
  4. Cancer Research UK
  5. Engineering and Physical Sciences Research Council [C1519/A16463]
  6. Medical Research Council
  7. Department of Health (England) [C1519/A16463]
  8. Cancer Research UK [16463] Funding Source: researchfish

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Background: Texture features are being increasingly evaluated in F-18-fluorodeoxyglucose positron emission tomography (F-18-FDG PET) as adjunctive imaging biomarkers in a number of different cancers. Whilst studies have reported repeatability between scans, there have been no studies that have specifically investigated the effect that the time of acquisition post-injection of F-18-FDG has on texture features. The aim of this study was to investigate if texture features change between scans performed at different time points post-injection. Results: Fifty-four patients (30 male, 24 female, mean age 35.1 years) with neurofibromatosis-1 and suspected malignant transformation of a neurofibroma underwent F-18-FDG PET/computed tomography (CT) scans at 101.5 +/- 15.0 and 251.7 +/- 18.4 min post-injection of 350 MBq F-18-FDG to a standard clinical protocol. Following tumour segmentation on both early and late scans, first- (n = 37), second- (n = 25) and high-order (n = 31) statistical features, as well as fractal texture features (n = 6), were calculated and a comparison was made between the early and late scans for each feature. Of the 54 tumours, 30 were benign and 24 malignant on histological analysis or on clinical follow-up for at least 5 years. Overall, 25/37 first-order, 9/25 second-order, 13/31 high-order and 3/6 fractal features changed significantly (p < 0.05) between early and late scans. The corresponding proportions for the 30 benign tumours alone were 22/37, 7/25, 8/31 and 2/6 and for the 24 malignant tumours, 11/37, 6/25, 8/31 and 0/6, respectively. Conclusions: Several texture features change with time post-injection of F-18-FDG. Thus, when comparing texture features in intra- and inter-patient studies, it is essential that scans are obtained at a consistent time post-injection of F-18-FDG.

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