To compare the interobserver agreement and degree of confidence in anatomical localisation of lesions using 2-[fluorine-18]fluoro-2-deoxy-
D
-glucose (
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F-FDG) positron emission tomography (PET)/computed tomography (CT) and
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F-FDG PET alone in patients with head and neck tumours. A prospective study of 24 patients (16 male, eight female, median age 59 years) with head and neck tumours was undertaken.
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F-FDG PET/CT was performed for staging purposes. 2D images were acquired over the head and neck area using a GE Discovery LS™ PET/CT scanner.
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F-FDG PET images were interpreted by three independent observers. The observers were asked to localise abnormal
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F-FDG activity to an anatomical territory and score the degree of confidence in localisation on a scale from 1 to 3 (1=exact region unknown; 2=probable; 3=definite). For all
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F-FDG-avid lesions, standardised uptake values (SUVs) were also calculated. After 3 weeks, the same exercise was carried out using
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F-FDG PET/CT images, where CT and fused volume data were made available to observers. The degree of interobserver agreement was measured in both instances. A total of six primary lesions with abnormal
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F-FDG uptake (SUV range 7.2–22) were identified on
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F-FDG PET alone and on
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F-FDG PET/CT. In all, 15 nonprimary tumour sites were identified with
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F-FDG PET only (SUV range 4.5–11.7), while 17 were identified on
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F-FDG PET/CT. Using
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F-FDG PET only, correct localisation was documented in three of six primary lesions, while
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F-FDG PET/CT correctly identified all primary sites. In nonprimary tumour sites,
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F-FDG PET/CT improved the degree of confidence in anatomical localisation by 51%. Interobserver agreement in assigning primary and nonprimary lesions to anatomical territories was moderate using
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F-FDG PET alone (kappa coefficients of 0.45 and 0.54, respectively), but almost perfect with
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F-FDG PET/CT (kappa coefficients of 0.90 and 0.93, respectively). We conclude that
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F-FDG PET/CT significantly increases interobserver agreement and confidence in disease localisation of
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F-FDG-avid lesions in patients with head and neck cancers.