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Prognostic implication of intratumoral metabolic heterogeneity in invasive ductal carcinoma of the breast

BACKGROUND: The purpose of this study was to evaluate the prognostic implication of findings of intratumoral metabolic heterogeneity on pretreatment (18)F-FDG PET/CT scans in patients with invasive ductal carcinoma (IDC) of the breast. METHODS: One hundred and twenty-three female IDC patients who un...

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Autores principales: Son, Seung Hyun, Kim, Do-Hoon, Hong, Chae Moon, Kim, Choon-Young, Jeong, Shin Young, Lee, Sang-Woo, Lee, Jaetae, Ahn, Byeong-Cheol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4148559/
https://www.ncbi.nlm.nih.gov/pubmed/25112709
http://dx.doi.org/10.1186/1471-2407-14-585
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author Son, Seung Hyun
Kim, Do-Hoon
Hong, Chae Moon
Kim, Choon-Young
Jeong, Shin Young
Lee, Sang-Woo
Lee, Jaetae
Ahn, Byeong-Cheol
author_facet Son, Seung Hyun
Kim, Do-Hoon
Hong, Chae Moon
Kim, Choon-Young
Jeong, Shin Young
Lee, Sang-Woo
Lee, Jaetae
Ahn, Byeong-Cheol
author_sort Son, Seung Hyun
collection PubMed
description BACKGROUND: The purpose of this study was to evaluate the prognostic implication of findings of intratumoral metabolic heterogeneity on pretreatment (18)F-FDG PET/CT scans in patients with invasive ductal carcinoma (IDC) of the breast. METHODS: One hundred and twenty-three female IDC patients who underwent pretreatment (18)F-fluorodeoxyglucose positron-emission tomography/computed tomography ((18)F-FDG PET/CT) scans were retrospectively evaluated in this study. The heterogeneity factor (HF) defined as the derivative (dV/dT) of a volume threshold function from 40% to 80%, was computed for each primary tumor. Other metabolic PET parameters (maximum standardized uptake value [SUVmax], metabolic tumor volume [MTV], and total lesion glycolysis [TLG]) were measured. The HF was compared with clinicopathologic factors and other PET parameters. Univariate and multivariate analyses for the overall survival (OS) were performed. RESULTS: The HF ranged from 0.02 to 6.72 (mean, 0.35 ± 0.82) and significantly correlated with MTV (r = 0.955; p < 0.0001) and TLG (r = 0.354; p = 0.0001). The HF was significantly higher (implying more heterogeneity) in tumors with higher T and N stages. The optimal cut-off values for the OS determined using a receiver operating characteristic (ROC) curve were 0.34 for the HF, 5.6 for SUVmax, 8.55 cm(3) for MTV, and 14.43 for TLG. The OS rate among the 123 patients was 86.2%. T stage (1, 2 vs. 3, 4), N stage (0, 1 vs. 2, 3), M stage (0 vs. 1), ER status (+ vs. –), SUVmax (≤ 5.6 vs. > 5.6), MTV (≤ 8.55 cm(3) vs. > 8.55 cm(3)), TLG (≤ 14.43 vs. > 14.43), and HF (< 0.34 vs. ≥ 0.34) affected the OS on univariate analysis. After adjustment for the effects of TNM stage and ER status, the HF and MTV were significant predictors of OS. Among the PET parameters, the best prognostic factor for OS was the HF. CONCLUSIONS: Intratumoral metabolic heterogeneity correlated closely with the MTV and significantly affected the OS in IDC patients. The HF may act as a robust surrogate marker for the prediction of OS in IDC patients.
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spelling pubmed-41485592014-08-29 Prognostic implication of intratumoral metabolic heterogeneity in invasive ductal carcinoma of the breast Son, Seung Hyun Kim, Do-Hoon Hong, Chae Moon Kim, Choon-Young Jeong, Shin Young Lee, Sang-Woo Lee, Jaetae Ahn, Byeong-Cheol BMC Cancer Research Article BACKGROUND: The purpose of this study was to evaluate the prognostic implication of findings of intratumoral metabolic heterogeneity on pretreatment (18)F-FDG PET/CT scans in patients with invasive ductal carcinoma (IDC) of the breast. METHODS: One hundred and twenty-three female IDC patients who underwent pretreatment (18)F-fluorodeoxyglucose positron-emission tomography/computed tomography ((18)F-FDG PET/CT) scans were retrospectively evaluated in this study. The heterogeneity factor (HF) defined as the derivative (dV/dT) of a volume threshold function from 40% to 80%, was computed for each primary tumor. Other metabolic PET parameters (maximum standardized uptake value [SUVmax], metabolic tumor volume [MTV], and total lesion glycolysis [TLG]) were measured. The HF was compared with clinicopathologic factors and other PET parameters. Univariate and multivariate analyses for the overall survival (OS) were performed. RESULTS: The HF ranged from 0.02 to 6.72 (mean, 0.35 ± 0.82) and significantly correlated with MTV (r = 0.955; p < 0.0001) and TLG (r = 0.354; p = 0.0001). The HF was significantly higher (implying more heterogeneity) in tumors with higher T and N stages. The optimal cut-off values for the OS determined using a receiver operating characteristic (ROC) curve were 0.34 for the HF, 5.6 for SUVmax, 8.55 cm(3) for MTV, and 14.43 for TLG. The OS rate among the 123 patients was 86.2%. T stage (1, 2 vs. 3, 4), N stage (0, 1 vs. 2, 3), M stage (0 vs. 1), ER status (+ vs. –), SUVmax (≤ 5.6 vs. > 5.6), MTV (≤ 8.55 cm(3) vs. > 8.55 cm(3)), TLG (≤ 14.43 vs. > 14.43), and HF (< 0.34 vs. ≥ 0.34) affected the OS on univariate analysis. After adjustment for the effects of TNM stage and ER status, the HF and MTV were significant predictors of OS. Among the PET parameters, the best prognostic factor for OS was the HF. CONCLUSIONS: Intratumoral metabolic heterogeneity correlated closely with the MTV and significantly affected the OS in IDC patients. The HF may act as a robust surrogate marker for the prediction of OS in IDC patients. BioMed Central 2014-08-12 /pmc/articles/PMC4148559/ /pubmed/25112709 http://dx.doi.org/10.1186/1471-2407-14-585 Text en © Son et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Son, Seung Hyun
Kim, Do-Hoon
Hong, Chae Moon
Kim, Choon-Young
Jeong, Shin Young
Lee, Sang-Woo
Lee, Jaetae
Ahn, Byeong-Cheol
Prognostic implication of intratumoral metabolic heterogeneity in invasive ductal carcinoma of the breast
title Prognostic implication of intratumoral metabolic heterogeneity in invasive ductal carcinoma of the breast
title_full Prognostic implication of intratumoral metabolic heterogeneity in invasive ductal carcinoma of the breast
title_fullStr Prognostic implication of intratumoral metabolic heterogeneity in invasive ductal carcinoma of the breast
title_full_unstemmed Prognostic implication of intratumoral metabolic heterogeneity in invasive ductal carcinoma of the breast
title_short Prognostic implication of intratumoral metabolic heterogeneity in invasive ductal carcinoma of the breast
title_sort prognostic implication of intratumoral metabolic heterogeneity in invasive ductal carcinoma of the breast
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4148559/
https://www.ncbi.nlm.nih.gov/pubmed/25112709
http://dx.doi.org/10.1186/1471-2407-14-585
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