Metabolic characterization of breast tumors with positron emission tomography using F-18 fluorodeoxyglucose

N. Avril, J. Dose, F. Jänicke, S. Bense, S. Ziegler, C. Laubenbacher, W. Römer, H. Pache, M. Herz, B. Allgayer, W. Nathrath, H. Graeff, M. Schwaiger

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244 Scopus citations

Abstract

Purpose: To evaluate the diagnostic value of positron emission tomographic (PET) imaging with F-18 fluorodeoxyglucose (FDG) in differentiating between benign and malignant breast tumors. Patients and Methods: Fifty-one patients, with suspicious breast lesions newly discovered either by physical examination or by mammography, underwent PET imaging before exploratory surgery. FDG-PET images of the breast were analyzed visually and quantitatively for objective assessment of regional tracer uptake. Results: Primary breast cancer was identified visually with a sensitivity of 68% to 94% and a specificity of 84% to 97% depending on criteria used for image interpretation. Quantitative analysis of FDG uptake in tumors using standardized uptake values (SUV) showed a significant difference between benign (1.4 ± 0.5) and malignant (3.3 ± 1.8) breast tumors (P < .01). Receiver operating characteristic (ROC) curve analysis exhibited a sensitivity of 75% and a specificity of 100% at a threshold SUV value of 2.5. Sensitivity increased to 92% with a corresponding specificity of 97% when partial volume correction of FDG uptake was performed based on independent anatomic information. Conclusion: PET imaging allowed accurate differentiation between benign and malignant breast tumors providing a high specificity. Sensitivity for detection of small breast cancer (< 1 cm) was limited due to partial volume effects. Quantitative image analysis combined with partial volume correction may be necessary to exploit fully the diagnostic accuracy. PET imaging may be helpful as a complimentary method in a subgroup of patients with indeterminate results of conventional breast imaging.

Original languageEnglish
Pages (from-to)1848-1857
Number of pages10
JournalJournal of Clinical Oncology
Volume14
Issue number6
DOIs
StatePublished - Jun 1996

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