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FDG PET/CT as a survival prognostic factor in patients with advanced renal cell carcinoma

Accurate prediction of the outcome of molecular target-based treatment in advanced renal cell carcinoma (RCC) is an important clinical problem. Positron emission tomography/computed tomography using [18F]-2-fluoro-2-deoxyglucose (FDG PET/CT) is a noninvasive tool for the assessment of glucose accumu...

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Autores principales: Pankowska, Violetta, Malkowski, Bogdan, Wedrowski, Mateusz, Wedrowska, Ewelina, Roszkowski, Krzysztof
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394561/
https://www.ncbi.nlm.nih.gov/pubmed/30488140
http://dx.doi.org/10.1007/s10238-018-0539-9
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author Pankowska, Violetta
Malkowski, Bogdan
Wedrowski, Mateusz
Wedrowska, Ewelina
Roszkowski, Krzysztof
author_facet Pankowska, Violetta
Malkowski, Bogdan
Wedrowski, Mateusz
Wedrowska, Ewelina
Roszkowski, Krzysztof
author_sort Pankowska, Violetta
collection PubMed
description Accurate prediction of the outcome of molecular target-based treatment in advanced renal cell carcinoma (RCC) is an important clinical problem. Positron emission tomography/computed tomography using [18F]-2-fluoro-2-deoxyglucose (FDG PET/CT) is a noninvasive tool for the assessment of glucose accumulation which can be a marker of the biological characteristics of the tumor. In this paper, we assess FDG PET/CT as a survival prognostic marker in patients with advanced RCC. The study included 121 patients treated in the years 2011–2016 with a diagnosis of advanced renal cell carcinoma (stage IV, multifocal metastases in all patients). Assessment using FDG PET/CT was conducted by measuring the maximum standard uptake value (SUVmax) for the marker used (the highest SUV measurement result for each patient in a single examination). SUVmax measurements were compared with various clinical risk factors used as prognostic markers. The median follow-up period was 19 months (ranging from 3 to 61 months). SUVmax measurements in all patients ranged from 1.3 to 30.0 (median 6.9). Higher SUVmax was correlated with poorer prognosis. Multi-way analysis with standard risk factors revealed that SUVmax was an independent factor for overall survival (OS; p < 0.003, hazard ratio 1.312, 95% CI 1.147–1.346). For SUVmax < 7.0, median OS was 32 months. For 7.0 ≤ SUVmax < 12.0, median OS was 12.5 months. For SUVmax ≥ 12.0, median OS was 10 months. The differences were statistically significant. A preliminary SUVmax assessment conducted using FDG PET/CT can provide information useful in the prediction of survival of patients with advanced RCC.
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spelling pubmed-63945612019-03-15 FDG PET/CT as a survival prognostic factor in patients with advanced renal cell carcinoma Pankowska, Violetta Malkowski, Bogdan Wedrowski, Mateusz Wedrowska, Ewelina Roszkowski, Krzysztof Clin Exp Med Original Article Accurate prediction of the outcome of molecular target-based treatment in advanced renal cell carcinoma (RCC) is an important clinical problem. Positron emission tomography/computed tomography using [18F]-2-fluoro-2-deoxyglucose (FDG PET/CT) is a noninvasive tool for the assessment of glucose accumulation which can be a marker of the biological characteristics of the tumor. In this paper, we assess FDG PET/CT as a survival prognostic marker in patients with advanced RCC. The study included 121 patients treated in the years 2011–2016 with a diagnosis of advanced renal cell carcinoma (stage IV, multifocal metastases in all patients). Assessment using FDG PET/CT was conducted by measuring the maximum standard uptake value (SUVmax) for the marker used (the highest SUV measurement result for each patient in a single examination). SUVmax measurements were compared with various clinical risk factors used as prognostic markers. The median follow-up period was 19 months (ranging from 3 to 61 months). SUVmax measurements in all patients ranged from 1.3 to 30.0 (median 6.9). Higher SUVmax was correlated with poorer prognosis. Multi-way analysis with standard risk factors revealed that SUVmax was an independent factor for overall survival (OS; p < 0.003, hazard ratio 1.312, 95% CI 1.147–1.346). For SUVmax < 7.0, median OS was 32 months. For 7.0 ≤ SUVmax < 12.0, median OS was 12.5 months. For SUVmax ≥ 12.0, median OS was 10 months. The differences were statistically significant. A preliminary SUVmax assessment conducted using FDG PET/CT can provide information useful in the prediction of survival of patients with advanced RCC. Springer International Publishing 2018-11-28 2019 /pmc/articles/PMC6394561/ /pubmed/30488140 http://dx.doi.org/10.1007/s10238-018-0539-9 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Pankowska, Violetta
Malkowski, Bogdan
Wedrowski, Mateusz
Wedrowska, Ewelina
Roszkowski, Krzysztof
FDG PET/CT as a survival prognostic factor in patients with advanced renal cell carcinoma
title FDG PET/CT as a survival prognostic factor in patients with advanced renal cell carcinoma
title_full FDG PET/CT as a survival prognostic factor in patients with advanced renal cell carcinoma
title_fullStr FDG PET/CT as a survival prognostic factor in patients with advanced renal cell carcinoma
title_full_unstemmed FDG PET/CT as a survival prognostic factor in patients with advanced renal cell carcinoma
title_short FDG PET/CT as a survival prognostic factor in patients with advanced renal cell carcinoma
title_sort fdg pet/ct as a survival prognostic factor in patients with advanced renal cell carcinoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394561/
https://www.ncbi.nlm.nih.gov/pubmed/30488140
http://dx.doi.org/10.1007/s10238-018-0539-9
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