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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.
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页码:152 / 158
页数:7
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