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Prognostic value of (18)F-fluorodeoxyglucose bone marrow uptake in patients with solid tumors: A meta-analysis

BACKGROUND: Several studies have reported the prognostic value of (18)F-fluorodeoxyglucose ((18)F-FDG) bone marrow uptake (BMU) measured by (18)F-FDG positron emission tomography ((18)F-FDG PET) in various cancers. We performed a meta-analysis to evaluate the prognostic value of (18)F-FDG BMU in pat...

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Autores principales: Jeong, Shin Young, Kim, Seong-Jang, Pak, Kyoungjune, Lee, Sang-Woo, Ahn, Byeong-Cheol, Lee, Jaetae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6221657/
https://www.ncbi.nlm.nih.gov/pubmed/30412079
http://dx.doi.org/10.1097/MD.0000000000012859
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author Jeong, Shin Young
Kim, Seong-Jang
Pak, Kyoungjune
Lee, Sang-Woo
Ahn, Byeong-Cheol
Lee, Jaetae
author_facet Jeong, Shin Young
Kim, Seong-Jang
Pak, Kyoungjune
Lee, Sang-Woo
Ahn, Byeong-Cheol
Lee, Jaetae
author_sort Jeong, Shin Young
collection PubMed
description BACKGROUND: Several studies have reported the prognostic value of (18)F-fluorodeoxyglucose ((18)F-FDG) bone marrow uptake (BMU) measured by (18)F-FDG positron emission tomography ((18)F-FDG PET) in various cancers. We performed a meta-analysis to evaluate the prognostic value of (18)F-FDG BMU in patients with solid tumors. METHODS: Systematic searches of MEDLINE and Embase databases were performed using the keywords “(18)F-FDG,” “bone marrow,” and “prognosis.” All published human studies of the prognostic value of (18)F-FDG BMU in patients with solid tumors were searched. The primary outcome was event-free survival (EFS), and the secondary endpoint was overall survival (OS); both of these were extracted directly from each study. The effects of (18)F-FDG BMU on survival were assessed by using hazard ratios (HRs). RESULTS: Ten studies with 1197 patients (8 studies reporting EFS in 1096 patients and 7 studies reporting OS in 836 patients) were included. In the EFS analysis, the combined HR was 1.75 (95% confidence interval [CI]: 1.45–2.11, P < .00001) in the random effects model (I(2) = 51%, P = .05). The combined HR of OS was 1.40 (95% CI: 1.13–1.73, P = .002) in the random effects model (I(2) = 52%, P = .05). CONCLUSION: This meta-analysis has demonstrated that patients with a low level of (18)F-FDG BMU have better EFS and OS than those with a high level of (18)F-FDG BMU. Based on our results, we suggest that (18)F-FDG BMU could be used as a biomarker for stratifying the risk of tumor progression in patients with solid tumors.
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spelling pubmed-62216572018-12-04 Prognostic value of (18)F-fluorodeoxyglucose bone marrow uptake in patients with solid tumors: A meta-analysis Jeong, Shin Young Kim, Seong-Jang Pak, Kyoungjune Lee, Sang-Woo Ahn, Byeong-Cheol Lee, Jaetae Medicine (Baltimore) Research Article BACKGROUND: Several studies have reported the prognostic value of (18)F-fluorodeoxyglucose ((18)F-FDG) bone marrow uptake (BMU) measured by (18)F-FDG positron emission tomography ((18)F-FDG PET) in various cancers. We performed a meta-analysis to evaluate the prognostic value of (18)F-FDG BMU in patients with solid tumors. METHODS: Systematic searches of MEDLINE and Embase databases were performed using the keywords “(18)F-FDG,” “bone marrow,” and “prognosis.” All published human studies of the prognostic value of (18)F-FDG BMU in patients with solid tumors were searched. The primary outcome was event-free survival (EFS), and the secondary endpoint was overall survival (OS); both of these were extracted directly from each study. The effects of (18)F-FDG BMU on survival were assessed by using hazard ratios (HRs). RESULTS: Ten studies with 1197 patients (8 studies reporting EFS in 1096 patients and 7 studies reporting OS in 836 patients) were included. In the EFS analysis, the combined HR was 1.75 (95% confidence interval [CI]: 1.45–2.11, P < .00001) in the random effects model (I(2) = 51%, P = .05). The combined HR of OS was 1.40 (95% CI: 1.13–1.73, P = .002) in the random effects model (I(2) = 52%, P = .05). CONCLUSION: This meta-analysis has demonstrated that patients with a low level of (18)F-FDG BMU have better EFS and OS than those with a high level of (18)F-FDG BMU. Based on our results, we suggest that (18)F-FDG BMU could be used as a biomarker for stratifying the risk of tumor progression in patients with solid tumors. Wolters Kluwer Health 2018-10-26 /pmc/articles/PMC6221657/ /pubmed/30412079 http://dx.doi.org/10.1097/MD.0000000000012859 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Research Article
Jeong, Shin Young
Kim, Seong-Jang
Pak, Kyoungjune
Lee, Sang-Woo
Ahn, Byeong-Cheol
Lee, Jaetae
Prognostic value of (18)F-fluorodeoxyglucose bone marrow uptake in patients with solid tumors: A meta-analysis
title Prognostic value of (18)F-fluorodeoxyglucose bone marrow uptake in patients with solid tumors: A meta-analysis
title_full Prognostic value of (18)F-fluorodeoxyglucose bone marrow uptake in patients with solid tumors: A meta-analysis
title_fullStr Prognostic value of (18)F-fluorodeoxyglucose bone marrow uptake in patients with solid tumors: A meta-analysis
title_full_unstemmed Prognostic value of (18)F-fluorodeoxyglucose bone marrow uptake in patients with solid tumors: A meta-analysis
title_short Prognostic value of (18)F-fluorodeoxyglucose bone marrow uptake in patients with solid tumors: A meta-analysis
title_sort prognostic value of (18)f-fluorodeoxyglucose bone marrow uptake in patients with solid tumors: a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6221657/
https://www.ncbi.nlm.nih.gov/pubmed/30412079
http://dx.doi.org/10.1097/MD.0000000000012859
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