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Positron emission tomography scanning in malignant melanoma
D S Tyler1, M Onaitis, A Kherani
1Department of Surgery, Duke University Medical Center, Durham, NC 27710, USA.
Cancer
|August 30, 2000
Summary
Positron emission tomography (PET) scans show 87.3% sensitivity for detecting Stage III malignant melanoma, aiding clinical management decisions in 15% of patients. PET is less effective for microscopic disease detection in earlier stages.
Area of Science:
- Oncology
- Nuclear Medicine
- Medical Imaging
Background:
- Anatomically based computed tomography (CT) scans have shown limited utility in evaluating Stage III malignant melanoma.
- Functional imaging is needed to improve diagnostic accuracy for advanced melanoma staging.
Purpose of the Study:
- To investigate the efficacy and clinical utility of positron emission tomography (PET) scans in patients with Stage III malignant melanoma.
- To compare PET scan performance against traditional imaging methods for melanoma staging.
Main Methods:
- Prospective evaluation of 106 whole-body 2-fluorine-18, 2-fluoro-2-deoxy-D-glucose (FDG) PET scans in 95 patients with Stage III melanoma.
- Identification of abnormal areas on FDG PET scans based on increased metabolic activity.
- Pathological assessment of all identified abnormal foci to confirm malignancy.
Main Results:
- PET scanning identified 144 of 165 melanoma sites (87.3% sensitivity), missing microscopic disease and smaller lesions.
- A positive predictive value of 78.6% was observed, improving to 90.6% with clinical information.
- Specificity was 43.5% due to limited lymph node dissections; 19.7% of abnormal PET findings indicated unsuspected metastatic disease.
- Clinical management plans were altered in 15.1% of patients based on PET scan results.
Conclusions:
- FDG PET scanning is a valuable tool for managing Stage III melanoma patients considered for further surgery.
- Despite a significant false-positive rate, PET scans influenced patient management in a notable percentage of cases.
- PET's limitations in detecting microscopic disease restrict its utility for Stage I-II melanoma evaluation.