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Published on: June 1, 2019
[PET scanning for malignant melanoma and positive sentinel node diagnostics]
Janne Horn1, Helle Sjøstrand, Jørgen Lock-Andersen
1Roskilde Sygehus, Plastikkirurgisk Afdeling, og Rigshospitalet, Diagnostisk Center, PET-og Cyclotronenheden, Denmark. janne@horn.dk
Positron emission tomography (PET) scans are not recommended for routine screening of melanoma patients with positive sentinel node biopsies. This diagnostic approach showed low sensitivity and specificity for detecting subclinical metastases.
Area of Science:
- Oncology
- Nuclear Medicine
- Diagnostic Imaging
Background:
- Melanoma staging often involves sentinel node biopsy (SNB) to detect lymph node metastasis.
- Subclinical metastases in melanoma patients with positive SNB require accurate detection methods.
- Positron emission tomography (PET) scanning is a potential tool for identifying distant spread.
Purpose of the Study:
- To evaluate the clinical utility of 18F-fluoro-2-deoxy-D-glucose (FDG) whole-body PET-scanning for detecting subclinical metastases.
- To assess the effectiveness of FDG-PET as a routine screening procedure in melanoma patients post-SNB.
- To determine the sensitivity and specificity of FDG-PET in this patient cohort.
Main Methods:
- Retrospective study of 80 melanoma patients with positive SNB and no clinical evidence of dissemination.
- Patients underwent FDG-PET scanning within 100 days of SNB and wide local excision.
- Follow-up averaged 30 months to assess recurrence and verify PET findings.
Main Results:
- 13 out of 80 patients (16.3%) had suspicious FDG-PET scans; 4 were true positives (5% of total).
- 67 patients had negative FDG-PET scans, but 4 (5.9%) developed clinical recurrence within 6 months (false negatives).
- FDG-PET demonstrated a sensitivity of 50% and a specificity of 31% for detecting subclinical metastases.
Conclusions:
- FDG-PET scanning is not a reliable routine investigation for melanoma patients with positive SNB.
- The diagnostic performance (sensitivity and specificity) is insufficient for clinical routine use.
- Alternative or additional staging methods may be necessary for this patient group.
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