Response monitoring in metastatic breast cancer: A comparison of survival times between FDG-PET/CT and CE-CT Journal Article


Authors: Naghavi-Behzad, M.; Vogsen, M.; Vester, R. M.; Olsen, M. M. B.; Oltmann, H.; Braad, P. E.; Asmussen, J. T.; Gerke, O.; Vach, W.; Kidholm, K.; Kodahl, A. R.; Weber, W.; Hildebrandt, M. G.
Article Title: Response monitoring in metastatic breast cancer: A comparison of survival times between FDG-PET/CT and CE-CT
Abstract: Background: We compared overall survival for metastatic breast cancer (MBC) patients monitored with CE-CT, FDG-PET/CT or a combination of them in an observational setting. Methods: Patients with biopsy-verified (recurrent or de novo) MBC (n = 300) who were treated at Odense university hospital (Denmark) and response monitored with FDG-PET/CT (n = 83), CE-CT (n = 144), or a combination of these (n = 73) were followed until 2019. Survival was compared between the scan groups, and were adjusted for clinico-histopathological variables representing potential confounders in a Cox proportional-hazard regression model. Results: The study groups were mostly comparable regarding baseline characteristics, but liver metastases were reported more frequently in CE-CT group (38.9%) than in FDG-PET/CT group (19.3%) and combined group (24.7%). Median survival was 30.0 months for CE-CT group, 44.3 months for FDG-PET/CT group and 54.0 months for Combined group. Five-year survival rates were significantly higher for FDG-PET/CT group (41.9%) and combined group (43.3%), than for CE-CT group (15.8%). Using the CE-CT group as reference, the hazard ratio was 0.44 (95% CI: 0.29–0.68, P = 0.001) for the FDG-PET/CT group after adjusting for baseline characteristics. FDG-PET/CT detected the first progression 4.7 months earlier than CE-CT, leading to earlier treatment change. Conclusions: In this single-center, observational study, patients with metastatic breast cancer who were response monitored with FDG-PET/CT alone or in combination with CE-CT had longer overall survival than patients monitored with CE-CT alone. Confirmation of these findings by further, preferably randomised clinical trials is warranted. © 2021, The Author(s), under exclusive licence to Springer Nature Limited.
Keywords: survival rate; positron emission tomography; radiopharmaceuticals; pathology; breast neoplasms; breast tumor; fluorodeoxyglucose f 18; fluorodeoxyglucose f18; positron-emission tomography; radiopharmaceutical agent; humans; human; female; positron emission tomography-computed tomography; positron emission tomography computed tomography
Journal Title: British Journal of Cancer
Volume: 126
Issue: 9
ISSN: 0007-0920
Publisher: Nature Publishing Group  
Date Published: 2022-05-18
Start Page: 1271
End Page: 1279
Language: English
DOI: 10.1038/s41416-021-01654-w
PUBMED: 35013575
PROVIDER: scopus
PMCID: PMC9042860
DOI/URL:
Notes: Article -- Export Date: 1 June 2022 -- Source: Scopus
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  1. Wolfgang Andreas Weber
    173 Weber