TY - JOUR
T1 - Diagnostic Accuracy of [18F]FDG PET/CT versus CT for NSCLC Surveillance
T2 - Secondary Analysis of a Randomized Clinical Trial
AU - Guldbrandsen, Kasper Foged
AU - Bloch, Martin
AU - Skougaard, Kristin
AU - Albrecht-Beste, Elisabeth
AU - Nellemann, Hanne Marie
AU - Krakauer, Martin
AU - Gørtz, Peter Michael
AU - Grüner, Julie Marie
AU - Fledelius, Joan
AU - Nielsen, Anne Lerberg
AU - Holdgaard, Paw Christian
AU - Nielsen, Søren Steen
AU - Hjorthaug, Karin
AU - Ahlborn, Lise Barlebo
AU - Jakobsen, Erik
AU - Højsgaard, Anette
AU - Petersen, Rene Horsleben
AU - Møller, Lars Borgbjerg
AU - Dahl, Morten
AU - Sorensen, Boe Sandahl
AU - Frank, Malene Støchkel
AU - Ehlers, Jeanette Haar
AU - Saghir, Zaigham
AU - Pøhl, Mette
AU - Borissova, Svetlana
AU - Land, Lotte Holm
AU - Kristiansen, Charlotte
AU - McCulloch, Tine
AU - Mortensen, Lise Saksø
AU - Christophersen, Malene Søby
AU - Hilberg, Ole
AU - Rasmussen, Thor Lind
AU - Schwaner, Signe Høyer Simonsen
AU - Laursen, Christian B
AU - Bodtger, Uffe
AU - Lonsdale, Markus Nowak
AU - Meyer, Christian Niels
AU - Gerke, Oke
AU - Mortensen, Jann
AU - Rasmussen, Torben Riis
AU - Fischer, Barbara Malene
AU - SUPE_R Study Group
N1 - Copyright © 2025 The Authors. Published by Elsevier Inc. All rights reserved.
PY - 2025/11/19
Y1 - 2025/11/19
N2 - BACKGROUND: Following curative treatment for non-small cell lung cancer (NSCLC), surveillance to detect recurrence is recommended. While computed tomography (CT) is the current standard for follow-up imaging, the optimal surveillance strategy remains debated. This study compares the diagnostic accuracy of fluorine-18 fluorodeoxyglucose positron emission tomography/computed tomography ([18F]FDG PET/CT; hereafter referred to as PET/CT) and CT for NSCLC surveillance.MATERIALS AND METHODS: This study represents a secondary analysis of data from a randomized controlled trial (SUPE_R, ClinicalTrials.gov NCT03740126) of patients with stage IA-IIIC NSCLC who completed curative-intent treatment between February 2019 and February 2022. CT and PET/CT scans were compared for recurrence detection using biopsy, multidisciplinary team assessment, or follow-up imaging as reference standards.RESULTS: The analysis included 899 PET/CT scans and 852 CT scans from 692 patients (mean age 69 years ± 8 [SD]; 412 female). For detecting recurrence, PET/CT demonstrated a higher sensitivity (88% [95% CI, 80%-93%] vs. 62% [95% CI, 50%-73%]; P < .001) but lower specificity (89% [95% CI, 86%-91%] vs. 96% [95% CI, 94%-97%]; P < .001) compared to CT. PET/CT demonstrated a higher sensitivity compared to CT after treatment with chemoradiotherapy (100% [95% CI, 72%-100%] vs. 46% [95% CI, 19%-75%]; P = .006) and at 0 to 6 month after treatment (83% [95% CI, 63%-94%] vs. 41% [95% CI, 21%-65%]; P = .008).CONCLUSION: The higher sensitivity of PET/CT, particularly after chemoradiotherapy and early post-treatment, suggests it may be particularly valuable in these high-risk scenarios. However, CT remains preferred for routine surveillance of low-risk patients given its superior specificity.
AB - BACKGROUND: Following curative treatment for non-small cell lung cancer (NSCLC), surveillance to detect recurrence is recommended. While computed tomography (CT) is the current standard for follow-up imaging, the optimal surveillance strategy remains debated. This study compares the diagnostic accuracy of fluorine-18 fluorodeoxyglucose positron emission tomography/computed tomography ([18F]FDG PET/CT; hereafter referred to as PET/CT) and CT for NSCLC surveillance.MATERIALS AND METHODS: This study represents a secondary analysis of data from a randomized controlled trial (SUPE_R, ClinicalTrials.gov NCT03740126) of patients with stage IA-IIIC NSCLC who completed curative-intent treatment between February 2019 and February 2022. CT and PET/CT scans were compared for recurrence detection using biopsy, multidisciplinary team assessment, or follow-up imaging as reference standards.RESULTS: The analysis included 899 PET/CT scans and 852 CT scans from 692 patients (mean age 69 years ± 8 [SD]; 412 female). For detecting recurrence, PET/CT demonstrated a higher sensitivity (88% [95% CI, 80%-93%] vs. 62% [95% CI, 50%-73%]; P < .001) but lower specificity (89% [95% CI, 86%-91%] vs. 96% [95% CI, 94%-97%]; P < .001) compared to CT. PET/CT demonstrated a higher sensitivity compared to CT after treatment with chemoradiotherapy (100% [95% CI, 72%-100%] vs. 46% [95% CI, 19%-75%]; P = .006) and at 0 to 6 month after treatment (83% [95% CI, 63%-94%] vs. 41% [95% CI, 21%-65%]; P = .008).CONCLUSION: The higher sensitivity of PET/CT, particularly after chemoradiotherapy and early post-treatment, suggests it may be particularly valuable in these high-risk scenarios. However, CT remains preferred for routine surveillance of low-risk patients given its superior specificity.
U2 - 10.1016/j.cllc.2025.11.011
DO - 10.1016/j.cllc.2025.11.011
M3 - Journal article
C2 - 41387040
SN - 1525-7304
JO - Clinical Lung Cancer
JF - Clinical Lung Cancer
ER -