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Published online before print July 23, 2004, 10.1148/radiol.2323030985

(Radiology 2004;232:823.)

A more recent version of this article appeared on September 1, 2004
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© RSNA, 2004

Nuclear Medicine

Non-Hodgkin Lymphoma and Hodgkin Disease: Coregistered FDG PET and CT at Staging and Restaging—Do We Need Contrast-enhanced CT?1

Niklaus G. Schaefer, MD2, Thomas F. Hany, MD, Christian Taverna, MD, Burkhardt Seifert, PhD, Katrin D. M. Stumpe, MD, Gustav K. von Schulthess, MD, PhD and Gerhard W. Goerres, MD

1 From the Departments of Nuclear Medicine (N.G.S., T.F.H., K.D.M.S., G.K.v.S., G.W.G.) and Internal Medicine (C.T.), University Hospital Zurich, Raemistrasse 100, CH-8091 Zurich, Switzerland; and Department of Biostatistics, University of Zurich, Switzerland (B.S.). Received June 23, 2003; revision requested August 29; final revision received February 2, 2004; accepted February 16. Address correspondence to G.W.G. (e-mail: gerhard.goerres@dmr.usz.ch).

PURPOSE: To retrospectively compare diagnostic value of coregistered fluorine 18 fluorodeoxyglucose positron emission tomographic (PET) and computed tomographic (CT) scans obtained with low-dose nonenhanced CT (PET/CT) with those routinely obtained with contrast material–enhanced CT for staging and restaging of disease in patients with Hodgkin disease or high-grade non-Hodgkin lymphoma.

MATERIALS AND METHODS: Sixty patients (mean age, 39.6 years ± 17.1 [standard deviation]) with Hodgkin disease (n = 42) or high-grade non-Hodgkin lymphoma (n = 18) were included in this retrospective study. All patients underwent PET/CT and contrast-enhanced CT within a maximum of 24 days (mean, 9.1 days ± 7.0) of each other for staging (n = 19) or first follow-up examination (n = 41). Findings were extracted from original written reports (PET/CT, contrast-enhanced CT) and compared with findings of reference standard, which included biopsy or follow-up with clinical, laboratory, or other imaging findings. For statistical analysis, sensitivity and specificity were calculated with findings of the reference standard. Agreement of both methods was determined with Cohen {kappa} and McNemar tests on a per-patient basis.

RESULTS: For evaluation of lymph node involvement, sensitivity of PET/CT and contrast-enhanced CT was 94% and 88%, and specificity was 100% and 86%, respectively. For evaluation of organ involvement, sensitivity of PET/CT and contrast-enhanced CT was 88% and 50%, and specificity was 100% and 90%, respectively. Agreement of both methods was excellent ({kappa} = 0.84) for assignment of lymph node involvement but only fair ({kappa} = 0.50) for extranodal disease. A difference with P < .05 (McNemar test) was considered significant in regard to exclusion of disease with PET/CT, compared with contrast-enhanced CT.

CONCLUSION: PET/CT performed with nonenhanced CT is more sensitive and specific than is contrast-enhanced CT for evaluation of lymph node and organ involvement, especially regarding exclusion of disease, in patients with Hodgkin disease and high-grade non-Hodgkin lymphoma.

© RSNA, 2004

Index terms: Dual-modality imaging, PET/CT, 99.12919, 99.12963 • Hodgkin disease, CT, 99.12912 • Hodgkin disease, staging • Lymphoma, CT, 99.12912 • Lymphoma, PET, 99.12963 • Lymphoma, staging




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