Optimal scan time for fluorine-18 fluorodeoxyglucose positron emission tomography in breast cancer |
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Authors: | A. R. Boerner M. Weckesser H. Herzog T. Schmitz W. Audretsch U. Nitz H. G. Bender H.-W. Mueller-Gaertner |
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Affiliation: | (1) Department of Nuclear Medicine, University Hospital Düsseldorf, Germany, DE;(2) Institute of Medicine, Research Centre Jülich, Germany, DE;(3) Department of Senology, City Hospital Düsseldorf, Germany, DE;(4) Department of Gynaecology and Obstetrics, University Hospital Düsseldorf, Germany, DE |
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Abstract: | Fluorine-18 fluorodeoxyglucose positron emission tomography (FDG PET) has proven useful in the differentiation of various tumour entities, including breast cancer. In patients with primary breast cancer we performed a 3-h imaging protocol to examine possible improvements in tumour detectability and image contrast. Twenty-nine patients with primary breast cancer with a diameter of ≥2 cm that was demonstrated to be malignant by biopsy or surgery were injected with 370–740 MBq 18F-FDG and scanned in the prone position. Data were acquired 0–40 min, 1.5 h and 3.0 h after injection. After correction for measured attenuation, decay and scatter and iterative reconstruction, standardised uptake values (SUVs) and tumour-to-non-tumour and tumour-to-organ ratios were calculated. Visual analysis was performed using transverse, sagittal and coronal slices as well as 3D reprojection images. Tumour-to-non-tumour and tumour-to-organ ratios were significantly higher for the 3-h images than for the 1.5-h images. SUVs did not increase to the same extent. Lesion detectability was 83% in 1.5-h images compared to 93% in 3-h images. We conclude that tumour contrast in breast cancer is improved by starting the PET acquisition at 3 h p.i. rather than at 1.5 h p.i. Received 17 October and in revised form 8 December 1998 |
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Keywords: | : Breast cancer Fluorine-18 fluorodeoxyglucose Positron emission tomography Tumour-to-non-tumour ratio Contrast parameters |
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