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Prospective Assessment of Fluorine-18-Fluorodeoxyglucose-Positron Emission Tomography/Computed Tomography
Sif Homburg1, Charlotte Birk Christensen2, Magnus Pedersen3
1Department of Oncology, Copenhagen University Hospital, Herlev and Gentofte, 2730 Herlev, Denmark.
Abstract:
The activity of immune checkpoint inhibitors (ICIs) in patients with metastatic melanoma is often monitored using fluorine-18-fluorodeoxyglucose-positron emission tomography/computed tomography (FDG-PET/CT) scans. However, distinguishing disease progression (PD) from pseudoprogression (PsPD), where increased FDG uptake might reflect immune cell activity rather than tumor growth, remains a challenge. This prospective study compared the efficacy of dual-time point (DTP) FDG-PET/CT with modified response criteria (PERCIMT) in differentiating PsPD from PD. From July 2017-January 2021, 41 patients suspected to have PsPD on an evaluation scan were prospectively included (29 evaluable). A subsequent DTP FDG-PET/CT scan was conducted within 14 days, followed by a confirmatory FDG-PET/CT scan. Additionally, PERCIMT were applied. DTP FDG-PET/CT identified 24% with PsPD and 76% with PD. Applying PERCIMT criteria, 69% showed PsPD, while 31% had PD. On follow-up, 10 patients (34%) demonstrated confirmed PsPD, while 19 (66%) exhibited PD. The sensitivity and specificity of DTP FDG-PET/CT were 20% and 74%, respectively, and for PERCIMT this was 80% and 37%, respectively. Our findings suggest limited efficacy of DTP FDG-PET/CT in distinguishing PsPD from PD in ICI-treated patients with metastatic melanoma. The use of PERCIMT could complement clinical assessment and be incorporated in multidisciplinary team conferences for enhanced decision-making.
Insights
Dual-time point FDG-PET/CT scans show limited ability to distinguish pseudoprogression from disease progression in metastatic melanoma patients treated with immune checkpoint inhibitors. PERCIMT criteria may offer complementary value in clinical decision-making.
Area of Science:
- Oncology
- Radiology
- Immunotherapy
Background:
- Immune checkpoint inhibitors (ICIs) are crucial for metastatic melanoma treatment.
- Monitoring treatment response with FDG-PET/CT is challenged by distinguishing disease progression (PD) from pseudoprogression (PsPD).
- PsPD can manifest as increased FDG uptake due to immune cell infiltration, mimicking tumor growth.
Purpose of the Study:
- To prospectively evaluate the efficacy of dual-time point (DTP) FDG-PET/CT compared to PERCIMT criteria in differentiating PsPD from PD.
- To assess the diagnostic performance of these methods in patients with metastatic melanoma receiving ICIs.
Main Methods:
- Prospective study including 41 patients with suspected PsPD on initial evaluation.
- Subsequent DTP FDG-PET/CT scans within 14 days, followed by confirmatory scans.
- Application of modified PERCIMT criteria for response assessment.
Main Results:
- DTP FDG-PET/CT identified 24% PsPD and 76% PD; PERCIMT criteria identified 69% PsPD and 31% PD.
- Confirmatory follow-up revealed 34% confirmed PsPD and 66% confirmed PD.
- Sensitivity/specificity for DTP FDG-PET/CT: 20%/74%; for PERCIMT: 80%/37%.
Conclusions:
- DTP FDG-PET/CT demonstrates limited efficacy in differentiating PsPD from PD in ICI-treated metastatic melanoma.
- PERCIMT criteria show potential as a complementary tool for clinical assessment.
- Integration into multidisciplinary team conferences may enhance treatment decision-making for these patients.
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