Zusammenfassung
Fragestellung
Erste Ergebnisse der PET-CT bei Morbus Hodgkin (HD) und den aggressiven Non-Hodgkin-Lymphomen (NHL) werden beschrieben.
Patienten und Methoden
Von März 2001 bis August 2004 wurden 822 PET-CT bei Lymphompatienten zum primären Staging, zum Restaging nach Therapie und zur Rezidivdiagnostik an unserer Klinik durchgeführt. Für die Koregistration wurde ein Low-dose-CT ohne i.v.-Kontrastmittel verwendet.
Ergebnisse
Durch die exakte anatomische Zuordnung der 18F-FDG aufnehmenden Läsionen wurden unklare oder falsch-positive PET-Befunde vermieden. Die PET-CT erzielte im Vergleich zur KM-verstärkten CT eine höhere Sensitivität und Spezifität bei Patienten mit HD und aggressiven NHL. Die Integration der PET-CT in die Planung der Strahlentherapie führte zu einer Optimierung der Feldgrenzen.
Schlussfolgerung
Die PET-CT hat sich bereits in der Phase der initialen klinischen Evaluation als wertvoll beim Staging und Restaging von Lymphomen erwiesen. Die exakte anatomische Zuordnung der PET-Informationen ist für eine sichere Befundung, für die Planung einer Strahlentherapie und die Planung einer Operation zur Biopsie unerlässlich.
Abstract
Purpose
First results of PET/CT in Hodgkin’s disease (HD) and aggressive non-Hodgkin’s lymphoma (NHL) are reported.
Patients and methods
From March 2001 to August 2004 822 PET/CT were performed at our clinic in lymphoma patients for primary staging, restaging after therapy, and diagnosis of recurrence. For coregistration non contrast-enhanced low-dose CT were used.
Results
Due to the exact anatomic localization of 18F-FDG accumulating lesions equivocal or false positive PET findings are avoided. In comparison to contrast enhanced CT, PET/CT has a higher sensitivity and specificity in patients with HD and aggressive NHL. Integration of PET/CT in treatment planning of radiation therapy optimizes the field volume.
Conclusion
Even in the initial phase of clinical evaluation, PET/CT has proven useful in staging and restaging of lymphoma. The exact anatomic localization of the PET findings is essential for a precise report, for treatment planning of radiation therapy, and for planning surgical biopsy.
Literatur
Alavi A, Gupta N, Alberini JL et al. (2003) Positron tomography imaging in nonmalignant thoracic disorders. Semin Nucl Med 32:293–321
Bangerter M, Kotzerke J, Griesshammer M, Elsner K, Reske SN, Bergmann L (1999) Positron emission tomography with 18-fluorodeoxyglucose in the staging and follow-up of lymphoma in the chest. Acta Oncol 38:799–804
Barrington SF, Maisey MN (1996) Skeletal muscle uptake of fluorine-18-FDG: effect of oral diazepam. J Nucl Med 37:1127–1129
Bar-Shalom R, Yefremov N, Guralnik L et al. (2003) Clinical performance of PET/CT in evaluation of cancer: additional value for diagnostic imaging and patient management. J Nucl Med 44:1200–1209
Chandar S, Meltzer CC, McCook BM (2002) Physiologic uterine uptake of FDG during menstruation demonstrated with serial combined positron emission tomography and computed tomography. Clin Nucl Med 27:22–24
Ciernik IF, Dizendorf E, Baumert B et al. (2003) Radiation treatment planning with an integrated positron emission and computer tomography (PET/CT): a feasibility study. Int J Radiat Oncol Biol Phys 57:853–863
Cook GJ, Fogelman I, Maisey MN (1996) Normal physiological and benign pathological variants of 18-fluoro-2-deoxyglucose positron-emission tomography scanning: potential for error in interpretation. Semin Nucl Med 26:308–314
Dizendorf EV, Baumert BG, von Schulthess GK, Lütolf UM, Steinert HC (2003) Impact of whole-body18F-FDG PET on staging and management patients for radiation therapy. J Nucl Med 44:23–29
Engel H, Steinert H, Buck A, von Schulthess GK (1996) Whole-body PET: physiological and artifactual fluorodeoxyglucose accumulations. J Nucl Med 37:441–446
Fayad LM, Cohade C, Wahl RL, Fishman EK (2003) Sacral fractures: a potential pitfall of FDG positron emission tomography. AJR 181:1239–1243
Gambhir SS, Czernin J, Schwimmer J, Silvermam DH, Coleman RE, Phelps ME (2000) A tabulated summary of the FDG PET literature. J Nucl Med 42:1S–93S
Glatz S, Kotzerke J, Moog F, Sandherr M, Heimpel H, Reske S (1996) Vortäuschung eines mediastinalen Non-Hodgkin-Lymphomrezidivs durch diffuse Thymushyperplasie im18F-FDG-PET. Fortschr Röntgenstr 165:309–310
Hany TF, Gharehpapagh E, Kamel EM, Buck A, Himms-Hagen J, von Schulthess GK (2002) Brown adipose tissue: a factor to consider in symmetrical tracer uptake in the neck and upper chest region. Eur J Nucl Med Mol Imaging 29:1393–1398
Hany TF, Steinert HC, Goerres GW, Buck A, von Schulthess (2002) PET diagnostic accuracy: improvement with in-line PET-CT system: initial results. Radiology 225:575–581
Hoegerle S, Juengling F, Otte A, Altehoefer C, Moser EA, Nitzsche EU (1998) Combined FDG and [F-18]fluoride whole-body PET: a feasible two-in-one approach to cancer imaging? Radiology 209:253–258
Hoffmann E, Kletter K, Diemling M, Becherer A, Pfeffel F, Petkov V (1999) Positron emission tomography with fluorine-18–2-fluoro-2-deoxy-D-glucose (F-18-FDG) does not visualise extranodal B-cell lymphoma of the mucosa-associated lymphoid tissue (MALT)-type. Ann Oncol 10:1185–1189
Hueltenschmidt B, Sautter-Bihl ML, Lang O et al. (2001) Whole body positron emission tomography in the treatment of Hodgkin’s disease. Cancer 91:302–310
Jacobsson H, Celsing F, Ingvar M, Stone-Elander S, Larsson SA (1998) Accumulation of FDG in axillary sweat glands in hyperhidrosis: a pitfall in whole-body PET examination. Eur Radiol 8:482–483
Kamel EM, Goerres GW, Burger C, von Schulthess GK, Steinert HC (2002) Recurrent laryngeal nerve palsy in patients with lung cancer: detection with PET-CT image fusion—report of six cases. Radiology 224:153–156
Reske SN, Kotzerke J (2001) FDG-PET for clinical use. Results of the 3rd German Interdisciplinary Consensus Conference, „Onko-PET III“. Eur J Nucl Med 28:1707–1723
Reske SN (2003) PET and restaging of malignant lymphoma including residual masses and relapse. Eur J Nucl Med Mol Imaging 30 [suppl 1]:S89–S96
Schaefer NG, Hany TF, Taverna C, Stumpe KDM, von Schulthess GK, Goerres GW (2004) Coregistered18F-fluorodeoxyglucose positron emission tomography and computed tomography (PET/CT) in patients with aggressive non-Hodgkin lymphoma and Hodgkin’s disease: do we need contrast-enhanced CT? Radiology 232:823–829
Schiepers C, Filmont J-E, Czernin J (2003) PET for staging of Hodgkin’s disease and non-Hodgkin’s lymphoma. Eur J Nucl Med Mol Imaging 30 [suppl 1]:S89–S96
Schöder H, Larson SM, Yeung HWD (2004) PET/CT in oncology—integration into clinical management of lymphoma, melanoma and gastrointestinal malignancies. J Nucl Med 45:72S–81S
Spaepen K, Stroobants S, Verhoef G, Mortelmans L (2003) Positron emission tomography with [18F]FDG for therapy response monitoring in lymphoma patients. Eur J Nucl Med Mol Imaging 30 [suppl 1]:S97–S105
Stumpe KD, Urbinelli M, Steinert HC et al. (1998) Whole-body positron emission tomography using fluorodeoxyglucose for staging of lymphoma: effectiveness and comparison with computed tomography. Eur J Nucl Med 25:721–728
Tatlidil R, Jadvar H, Bading JR, Conti PS (2002) Incidental colonic fluorodeoxyglucose uptake: correlation with colonoscopic and histopathologic findings. Radiology 224:783–787
Tasumi M, Cohade C, Nakamoto Y, Wahl RL (2003) Fluorodeoxyglucose uptake in the aortic wall at PET/CT: a possible finding for active atherosclerosis. Radiology 229:831–837
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Steinert, H.C. PET-CT bei Lymphompatienten. Radiologe 44, 1060–1067 (2004). https://doi.org/10.1007/s00117-004-1121-x
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DOI: https://doi.org/10.1007/s00117-004-1121-x