Basal 18F-FDG PET/CT as a predictive biomarker of tumor response for neoadjuvant therapy in breast cancer

被引:3
|
作者
Garcia Vicente, A. M. [1 ]
Soriano Castrejon, A. [1 ]
Pruneda-Gonzalez, R. E. [2 ,3 ]
Fernandez Calvo, G. [2 ,3 ]
Munoz Sanchez, M. M. [4 ]
Alvarez Cabellos, R. [5 ]
Espinosa Aunion, R. [6 ]
Relea Calatayud, F. [7 ]
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] Univ Castilla La Mancha, IMACI Inst Appl Math Sci & Engn, E-13071 Ciudad Real, Spain
[4] Virgen de la Luz Hosp, Dept Oncol, Cuenca, Spain
[5] Virgen de la Salud Hosp, Dept Oncol, Toledo, Spain
[6] La Mancha Ctr Hosp, Dept Oncol, Ciudad Real, Spain
[7] Univ Gen Hosp, Dept Pathol, Ciudad Real, Spain
关键词
Locally advanced breast cancer; F-18-FDG PET/CT; Tumor kinetics; Molecular phenotypes; Neoadjuvant chemotherapy response; EMISSION TOMOGRAPHY/COMPUTED TOMOGRAPHY; CHEMOTHERAPY; METABOLISM;
D O I
10.1016/j.remn.2015.09.001
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
Purpose: To explore the relation between tumor kinetic assessed by F-18-FDG PET and final neoadjuvant chemotherapy (NC) response within a molecular phenotype perspective. Material and Methods: Prospective study included 144 women with breast cancer. All patients underwent a dual-time point F-18-FDG PET/CT previous to NC. The retention index (RI), between SUV-1 and SUV-2 was calculated. Molecular subtypes were re-grouped in low, intermediate and high-risk biological phenotypes. After NC, all residual primary tumor specimens were histopathologically classified in tumor regression grades (TRG) and response groups. The relation between SUV-1, SUV-2 and RI with the TRG and response groups was evaluated in all molecular subtypes and in accordance with the risk categories. Results: Responder's lesions showed significant greater SUVmax compared to non-responders. The RI value did not show any significant relation with response. Attending to molecular phenotypes, statistical differences were observed with greater SUV for responders having high-risk molecular subtypes. Conclusion: Glycolytic tumor characteristics showed a significant correlation with NC response and dependence of risk phenotype. (C) 2015 Elsevier Espana, S.L.U. and SEMNIM. All rights reserved.
引用
收藏
页码:81 / 87
页数:7
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