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Role of quantitative imaging biomarkers in an early FDG-PET/CT for detection of immune-related adverse events in melanoma patients: a prospective study
To evaluate the role of the novel quantitative imaging biomarker (QIB) SUV of F-FDG uptake extracted from early F-FDG-PET/CT scan at 4 weeks for the detection of immune-related adverse events (rAE) in a cohort of patients with metastatic melanoma (mM) patients receiving immune-checkpoint inhibitors...
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Published in: | Radiology and oncology 2024-09, Vol.58 (3), p.335-347 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | To evaluate the role of the novel quantitative imaging biomarker (QIB) SUV
of
F-FDG uptake extracted from early
F-FDG-PET/CT scan at 4 weeks for the detection of immune-related adverse events (rAE) in a cohort of patients with metastatic melanoma (mM) patients receiving immune-checkpoint inhibitors (ICI).
In this prospective non-interventional, one-centre clinical study, patients with mM, receiving ICI treatment, were regularly followed by
F-FDG PET/CT. Patients were scanned at baseline, early point at week four (W4), week sixteen (W16) and week thirty-two (W32) after ICI initiation. A convolutional neural network (CNN) was used to segment three organs: lung, bowel, thyroid. QIB of irAE - SUV
- was analyzed within the target organs and correlated with the clinical irAE status. Area under the receiver-operating characteristic curve (AUROC) was used to quantify irAE detection performance.
A total of 242
F-FDG PET/CT images of 71 mM patients were prospectively collected and analysed. The early W4 scan showed improved detection only for the thyroid gland compared to W32 scan (p=0.047). The AUROC for detection of irAE in the three target organs was highest when SUV
was extracted from W16 scan and was 0.76 for lung, 0.53 for bowel and 0.81 for thyroid. SUV
extracted from W4 scan did not improve detection of irAE compared to W16 scan (lung: p = 0.54, bowel: p = 0.75, thyroid: p = 0.3, DeLong test), as well as compared to W32 scan in lungs (p = 0.32) and bowel (p = 0.3).
Early time point
F-FDG PET/CT at W4 did not lead to statistically significant earlier detection of irAE. However, organ
F-FDG uptake as quantified by SUV
proved to be a consistent QIB of irAE. To better assess the role of
F-FDG PET/CT in irAE detection, the time evolution of
F-FDG PET/CT quantifiable inflammation would be of essence, only achievable in multi centric studies. |
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ISSN: | 1581-3207 1318-2099 1581-3207 0485-893X |
DOI: | 10.2478/raon-2024-0045 |