[18F]2-fluoro-2-deoxy-D-glucose positron emission tomography (FDG PET) as a diagnostic tool for neurofibromatosis 1 (NF1) associated malignant peripheral nerve sheath tumours (MPNSTs):: a long-term clinical study

被引:169
作者
Ferner, R. E.
Golding, J. F.
Smith, M.
Calonje, E.
Jan, W.
Sanjayanathan, V.
O'Doherty, M.
机构
[1] Department of Neurology, Guy's and St Thomas' NHS Foundation Trust, Kings College London, London SE1 9RT, St Thomas' Street
[2] Department of Psychology, University of Westminster, London
[3] Department of Orthopaedics, Guy's and St Thomas' NHS Foundation Trust, London SE1 9RT, St Thomas' Street
[4] Department of Dermatopathology, Guy's and St Thomas' NHS Foundation Trust, London SE1 9RT, St Thomas' Street
[5] Department of Radiology, Guy's and St Thomas' NHS Foundation Trust, London SE1 9RT, St Thomas' Street
[6] Clinical PET Centre, Guy's and St Thomas' NHS Foundation Trust, Kings College London, London SE1 9RT, St Thomas' Street
关键词
FDG PET; malignant peripheral nerve sheath tumour; neurofibromatosis; 1; plexiform neurofibroma;
D O I
10.1093/annonc/mdm450
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Malignant peripheral nerve sheath tumours (MPNSTs) are difficult to detect in neurofibromatosis 1 (NF1) individuals. The purpose was to evaluate [F-18]2-fluoro-2-deoxy-D-glucose positron emission tomography (FDG PET) and PET computed tomography (CT) as a diagnostic tool for MPNST in NF1 patients with symptomatic plexiform neurofibromas and to verify the diagnosis by pathology and clinical follow-up. Patients and methods: NF1 individuals with symptomatic plexiform neurofibromas underwent clinical evaluation and magnetic resonance imaging. Qualitative FDG PET and PET CT associated with semi-quantitative maximum standard uptake value (SUVmax) assessed possible malignant change. Excision/biopsy verified the diagnosis when possible and clinical follow-up was undertaken in all patients. Results: In all, 116 lesions were detected in 105 patients aged 5-71 years, including 80 plexiform neurofibromas, five atypical neurofibromas, 29 MPNST and two other cancers. Biopsy confirmed the findings in 59 tumours and no MPNST was diagnosed on clinical follow-up of 23 lesions diagnosed as benign on FDG PET and PET CT. FDG PET and PET CT diagnosed NF1-associated tumours with a sensitivity of 0.89 [95% confidence interval (CI) 0.76-0.96] and a specificity of 0.95 (CI 0.88-0.98), but the SUVmax level did not predict tumour grade. Conclusion: FDG PET and PET CT is a sensitive and specific diagnostic tool for NF1-associated MPNST. Other PET tracers will be required to solve the problem of predicting tumour grade.
引用
收藏
页码:390 / 394
页数:5
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