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FDG-PET/CT for Response Monitoring in Metastatic Breast Cancer: The Feasibility and Benefits of Applying PERCIST

Background: We aimed to examine the feasibility and potential benefit of applying PET Response Criteria in Solid Tumors (PERCIST) for response monitoring in metastatic breast cancer (MBC). Further, we introduced the nadir scan as a reference. Methods: Response monitoring FDG-PET/CT scans in 37 women...

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Autores principales: Vogsen, Marianne, Bülow, Jakob Lykke, Ljungstrøm, Lasse, Oltmann, Hjalte Rasmus, Alamdari, Tural Asgharzadeh, Naghavi-Behzad, Mohammad, Braad, Poul-Erik, Gerke, Oke, Hildebrandt, Malene Grubbe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8073831/
https://www.ncbi.nlm.nih.gov/pubmed/33921580
http://dx.doi.org/10.3390/diagnostics11040723
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author Vogsen, Marianne
Bülow, Jakob Lykke
Ljungstrøm, Lasse
Oltmann, Hjalte Rasmus
Alamdari, Tural Asgharzadeh
Naghavi-Behzad, Mohammad
Braad, Poul-Erik
Gerke, Oke
Hildebrandt, Malene Grubbe
author_facet Vogsen, Marianne
Bülow, Jakob Lykke
Ljungstrøm, Lasse
Oltmann, Hjalte Rasmus
Alamdari, Tural Asgharzadeh
Naghavi-Behzad, Mohammad
Braad, Poul-Erik
Gerke, Oke
Hildebrandt, Malene Grubbe
author_sort Vogsen, Marianne
collection PubMed
description Background: We aimed to examine the feasibility and potential benefit of applying PET Response Criteria in Solid Tumors (PERCIST) for response monitoring in metastatic breast cancer (MBC). Further, we introduced the nadir scan as a reference. Methods: Response monitoring FDG-PET/CT scans in 37 women with MBC were retrospectively screened for PERCIST standardization and measurability criteria. One-lesion PERCIST based on changes in SULpeak measurements of the hottest metastatic lesion was used for response categorization. The baseline (PERCIST(baseline)) and the nadir scan (PERCIST(nadir)) were used as references for PERCIST analyses. Results: Metastatic lesions were measurable according to PERCIST in 35 of 37 (94.7%) patients. PERCIST was applied in 150 follow-up scans, with progression more frequently reported by PERCIST(nadir) (36%) than PERCIST(baseline) (29.3%; p = 0.020). Reasons for progression were (a) more than 30% increase in SUL(peak) of the hottest lesion (n = 7, 15.9%), (b) detection of new metastatic lesions (n = 28, 63.6%), or both (a) and (b) (n = 9, 20.5%). Conclusions: PERCIST, with the introduction of PERCIST(nadir), allows a graphical interpretation of disease fluctuation that may be beneficial in clinical decision-making regarding potential earlier termination of non-effective toxic treatment. PERCIST seems feasible for response monitoring in MBC but prospective studies are needed to come this closer.
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spelling pubmed-80738312021-04-27 FDG-PET/CT for Response Monitoring in Metastatic Breast Cancer: The Feasibility and Benefits of Applying PERCIST Vogsen, Marianne Bülow, Jakob Lykke Ljungstrøm, Lasse Oltmann, Hjalte Rasmus Alamdari, Tural Asgharzadeh Naghavi-Behzad, Mohammad Braad, Poul-Erik Gerke, Oke Hildebrandt, Malene Grubbe Diagnostics (Basel) Article Background: We aimed to examine the feasibility and potential benefit of applying PET Response Criteria in Solid Tumors (PERCIST) for response monitoring in metastatic breast cancer (MBC). Further, we introduced the nadir scan as a reference. Methods: Response monitoring FDG-PET/CT scans in 37 women with MBC were retrospectively screened for PERCIST standardization and measurability criteria. One-lesion PERCIST based on changes in SULpeak measurements of the hottest metastatic lesion was used for response categorization. The baseline (PERCIST(baseline)) and the nadir scan (PERCIST(nadir)) were used as references for PERCIST analyses. Results: Metastatic lesions were measurable according to PERCIST in 35 of 37 (94.7%) patients. PERCIST was applied in 150 follow-up scans, with progression more frequently reported by PERCIST(nadir) (36%) than PERCIST(baseline) (29.3%; p = 0.020). Reasons for progression were (a) more than 30% increase in SUL(peak) of the hottest lesion (n = 7, 15.9%), (b) detection of new metastatic lesions (n = 28, 63.6%), or both (a) and (b) (n = 9, 20.5%). Conclusions: PERCIST, with the introduction of PERCIST(nadir), allows a graphical interpretation of disease fluctuation that may be beneficial in clinical decision-making regarding potential earlier termination of non-effective toxic treatment. PERCIST seems feasible for response monitoring in MBC but prospective studies are needed to come this closer. MDPI 2021-04-19 /pmc/articles/PMC8073831/ /pubmed/33921580 http://dx.doi.org/10.3390/diagnostics11040723 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Vogsen, Marianne
Bülow, Jakob Lykke
Ljungstrøm, Lasse
Oltmann, Hjalte Rasmus
Alamdari, Tural Asgharzadeh
Naghavi-Behzad, Mohammad
Braad, Poul-Erik
Gerke, Oke
Hildebrandt, Malene Grubbe
FDG-PET/CT for Response Monitoring in Metastatic Breast Cancer: The Feasibility and Benefits of Applying PERCIST
title FDG-PET/CT for Response Monitoring in Metastatic Breast Cancer: The Feasibility and Benefits of Applying PERCIST
title_full FDG-PET/CT for Response Monitoring in Metastatic Breast Cancer: The Feasibility and Benefits of Applying PERCIST
title_fullStr FDG-PET/CT for Response Monitoring in Metastatic Breast Cancer: The Feasibility and Benefits of Applying PERCIST
title_full_unstemmed FDG-PET/CT for Response Monitoring in Metastatic Breast Cancer: The Feasibility and Benefits of Applying PERCIST
title_short FDG-PET/CT for Response Monitoring in Metastatic Breast Cancer: The Feasibility and Benefits of Applying PERCIST
title_sort fdg-pet/ct for response monitoring in metastatic breast cancer: the feasibility and benefits of applying percist
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8073831/
https://www.ncbi.nlm.nih.gov/pubmed/33921580
http://dx.doi.org/10.3390/diagnostics11040723
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