Detection of Recurrence After Thoracic Stereotactic Ablative Radiotherapy Using FDG-PET-CT
- PMID: 35246393
- DOI: 10.1016/j.cllc.2022.01.006
Detection of Recurrence After Thoracic Stereotactic Ablative Radiotherapy Using FDG-PET-CT
Abstract
Introduction/background: Differentiating local recurrence (LR) from post-treatment changes following stereotactic ablative radiotherapy (SABR) for thoracic tumors is challenging. We sought to evaluate the performance of FDG-PET-CT in distinguishing recurrence from post-radiation changes in patients with stage I-II non-small cell lung cancer (NSCLC) treated with SABR.
Materials and methods: We performed a retrospective review of patients with stage I-II NSCLC treated with SABR and subsequently followed with surveillance FDG-PET-CT scans from 2004 to 2014. The radiology reports were coded as 0 or 1 if minimally or substantially concerning for LR, respectively, and correlated with outcome. Prognostic factors for false-positive FDG-PET-CT were assessed using logistic regression models.
Results: We identified 145 patients meeting inclusion criteria for the retrospective analysis. Amongst the 39 (26.9%) patients with FDG-PET-CT scans concerning for LR 3 to 24 months after treatment, 14 were confirmed to have LR. Thus, the positive predictive value (PPV) of FDG-PET-CT in identifying LR was 36% (14/39). Factors associated with a false-positive scan included concerning FDG-PET-CT at the earliest post-treatment time point (3 months) (odds ratio 0.67, P= .04) and older age (odds ratio 2.3, P= .02).
Conclusion: Our analysis indicates that the PPV of a concerning FDG-PET-CT after SABR for early-stage NSCLC is relatively low, especially at early post-treatment timepoints, but accuracy is improving over time with institutional experience.
Keywords: (18)F-fluorodeoxyglucose-positron emission tomography; Local recurrence; Non–small cell lung cancer; Positive predictive value; Stereotactic Ablative Radiotherapy.
Copyright © 2022. Published by Elsevier Inc.
Conflict of interest statement
Conflicts of Interest The authors declare no conflicts of interest related to this work. B.W.L. has received research support from Varian Medical Systems, and is a co-founder and board member of TibaRay. M.D. has received research support from Varian Medical Systems, Illumina, AstraZeneca; paid consultancy from Roche, AstraZeneca, BioNTech, RefleXion, Genentech, Illumina, Gritstone Oncology, Novartis, Boehringer Ingelheim; travel honoraria from Roche and stock options from Foresight Diagnostics, CiberMed. All other authors have none.
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