Glycolytic activity in breast cancer using 18F-FDG PET/CT as prognostic predictor: A molecular phenotype approach

被引:6
作者
Garcia Vicente, A. M. [1 ]
Soriano Castrejon, A. [1 ]
Amo-Salas, M. [2 ]
Lopez Fidalgo, J. F. [2 ]
Munoz Sanchez, M. M. [3 ]
Alvarez Cabellos, R. [4 ]
Espinosa Aunion, R. [5 ]
Munoz Madero, V. [6 ]
机构
[1] Univ Gen Hosp, Dept Nucl Med, Ciudad Real, Spain
[2] Univ Castilla La Mancha, Dept Math, E-13071 Ciudad Real, Spain
[3] Virgen de la Luz Hosp, Dept Oncol, Cuenca, Spain
[4] Virgen de la Salud Hosp, Dept Oncol, Toledo, Spain
[5] La Mancha Ctr Hosp, Dept Oncol, Ciudad Real, Spain
[6] Gomez Ulla Hosp, Dept Surg, Madrid, Spain
来源
REVISTA ESPANOLA DE MEDICINA NUCLEAR E IMAGEN MOLECULAR | 2016年 / 35卷 / 03期
关键词
Breast cancer; F-18-FDG PET/CT; Molecular phenotypes; Prognosis; Disease free status; Disease free survival; Overall survival; POSITRON-EMISSION-TOMOGRAPHY; NEOADJUVANT CHEMOTHERAPY; HER-2/NEU ONCOGENE; TUMOR METABOLISM; SUBTYPES; RECURRENCE; PARAMETERS; RELEVANCE; CONSENSUS; SURVIVAL;
D O I
10.1016/j.remn.2015.08.001
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Aim: To explore the relationship between basal F-18-FDG uptake in breast tumors and survival in patients with breast cancer (BC) using a molecular phenotype approach. Material and Methods: This prospective and multicentre study included 193 women diagnosed with BC. All patients underwent an F-18-FDG PET/CT prior to treatment. Maximum standardized uptake value (SUVmax) in tumor (T), lymph nodes (N), and the N/T index was obtained in all the cases. Metabolic stage was established. As regards biological prognostic parameters, tumors were classified into molecular sub-types and risk categories. Overall survival (OS) and disease free survival (DFS) were obtained. An analysis was performed on the relationship between semi-quantitative metabolic parameters with molecular phenotypes and risk categories. The effect of molecular sub-type and risk categories in prognosis was analyzed using Kaplan-Meier and univariate and multivariate tests. Results: Statistical differences were found in both SUVT and SUVN, according to the molecular sub-types and risk classifications, with higher semi-quantitative values in more biologically aggressive tumors. No statistical differences were observed with respect to the N/T index. Kaplan-Meier analysis revealed that risk categories were significantly related to DFS and OS. In the multivariate analysis, metabolic stage and risk phenotype showed a significant association with DFS. Conclusion: High-risk phenotype category showed a worst prognosis with respect to the other categories with higher SUVmax in primary tumor and lymph nodes. (C) 2015 Elsevier Espana, S.L.U. and SEMNIM. All rights reserved.
引用
收藏
页码:152 / 158
页数:7
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