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Clinical Investigations |
1 PET Center, Groningen University Hospital, Groningen, The Netherlands
2 Department of Surgical Oncology, Groningen University Hospital, Groningen, The Netherlands
3 Department of Pathology and Laboratory Medicine, Groningen University Hospital, Groningen, The Netherlands
In this study, the feasibility of 3'-18F-fluoro-3'-deoxy-L-thymidine PET (18F-FLT PET) for staging patients with clinical stage III melanoma was investigated. Methods: Ten patients with melanoma and metastases to the locoregional draining lymph nodes, clinical stage IIIbased on physical examination, chest radiography, lactate dehydrogenase, and histopathologic confirmationunderwent a whole-body 18F-FLT PET scan 1 h after injection of a median 400-MBq dose (range, 185430 MBq) of 18F-FLT. All 18F-FLT PET lesions were verified using the American Joint Committee on Cancer Staging System, which includes physical examination, spiral CT, ultrasound, chest radiography, and histopathologic examinations. Size and mitotic rate of metastatic lymph nodes and skin metastases were determined. Results: All histopathologic samples and 18F-FLT PET lesions were categorized over anatomic regions and correlated. All locoregional metastases were correctly visualized by 18F-FLT PET. Region-based sensitivity for detection of lymph node metastatic disease was 88%. There were 3 true-negative and 2 false-positive lesions. The detection limit for lymph node metastases appeared to be approximately 6 mm or a mitotic rate of 9 mitoses per 2 mm2. Two patients were upstaged by 18F-FLT PET, which was confirmed by CT. In 3 patients, 18F-FLT PET detected a total of 3 additional lesions with therapeutic consequences, without influencing staging. These lesions were initially missed by clinical staging. Conclusion: 18F-FLT PET seems promising for (re)staging purposes in clinical stage III melanoma. Further research is needed, in which 18F-FLT PET should be compared with 18F-FDG PET.
Key Words: 3'-18F-fluoro-3'-deoxy-L-thymidine melanoma staging PET
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