Annals of Oncology 14:123-130, 2003
© 2003 European Society for Medical Oncology
Original Paper |
Early detection of relapse by whole-body positron emission tomography in the follow-up of patients with Hodgkins disease
1 Department of Medicine, Division of Medical Oncology and Hematology and 2 Division of Nuclear Medicine, University of Liège, Liège, Belgium
Received 18 February 2002; revised 4 June 2002; accepted 17 July 2002
Background:
Relapse after treatment of Hodgkins disease (HD) is usually identified as a result of the investigation of symptoms. We undertook this study to examine the value of whole-body positron emission tomography (PET) for the detection of preclinical relapse.
Patients and methods:
Thirty-six patients underwent 2-[fluorine-18]fluoro-2-deoxy-D-glucose (18F-FDG) PET at the end of treatment and than every 46 months for 23 years after the end of polychemotherapy and/or radiotherapy. In those cases of abnormal 18F-FDG accumulation a confirmatory study was performed 46 weeks later.
Results:
One patient had residual tumor and four patients relapsed during a follow-up of 524 months. All five events were correctly identified early by 18F-FDG PET. Residual tumor or relapse was never first diagnosed based on clinical examination, laboratory findings or computed tomography (CT) studies. Two patients presented B symptoms and the three others were asymptomatic at the time of residual disease or relapse. Confirmation of residual disease or relapse was obtained by biopsy in four patients 1, 1, 5 and 9 months after PET and by unequivocal clinical symptoms and CT studies in one patient 3 months after PET. False-positive 18F-FDG PET studies incorrectly suggested possible relapse in six other patients, but the confirmatory PET was always negative. Our study also provides important information about physiological 18F-FDG uptake in the thymus.
Conclusions:
Our data suggest the potential of 18F-FDG PET to detect preclinical relapse in patients with HD. This could help identify patients requiring salvage chemotherapy at the time of minimal disease rather than at the time of clinically overt relapse. Further studies are warranted to determine the impact of PET on treatment management and outcome. In fact, the aim of follow-up procedures is not only to detect preclinical relapse but mainly to obtain better results by starting salvage treatment earlier. A costbenefit analysis will also be necessary before 18F-FDG PET can be used routinely in the follow-up of patients with HD.
Key-words: 2-[fluorine-18]fluoro-2-deoxy-D-glucose, follow-up, Hodgkins disease, positron emission tomography, radionuclide imaging, relapse
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