18F-FDG PET/CT predicts survival in patients with inflammatory breast cancer undergoing neoadjuvant chemotherapy

被引:16
|
作者
Carkaci, Selin [1 ,7 ]
Sherman, Christopher T. [1 ]
Ozkan, Efe [1 ]
Adrada, Beatriz E. [1 ]
Wei, Wei [2 ]
Rohren, Eric M. [3 ]
Mawlawi, Osama R. [4 ]
Ueno, Naoto T. [5 ]
Buchholz, Thomas A. [6 ]
Yang, Wei T. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Diagnost Radiol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Nucl Med, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Imaging Phys, Houston, TX 77030 USA
[5] Univ Texas MD Anderson Canc Ctr, Morgan Welch Inflammatory Breast Canc Res Program, Dept Breast Med Oncol, Houston, TX 77030 USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Radiat Oncol, Houston, TX 77030 USA
[7] Ohio State Univ, Dept Radiol, Columbus, OH 43210 USA
关键词
Inflammatory breast cancer; F-18-FDG; PET/CT; Neoadjuvant chemotherapy; Survival; POSITRON-EMISSION-TOMOGRAPHY; PREOPERATIVE CHEMOTHERAPY; BLOOD-FLOW; TUMOR; THERAPY; FLUORODEOXYGLUCOSE; METABOLISM; MASTECTOMY; CARCINOMA;
D O I
10.1007/s00259-013-2506-8
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 The objective of this study was to evaluate the role of F-18-FDG PET/CT in predicting overall survival in inflammatory breast cancer patients undergoing neoadjuvant chemotherapy. Methods Included in this retrospective study were 53 patients with inflammatory breast cancer who had at least two PET/CT studies including a baseline study before the start of neoadjuvant chemotherapy. Univariate and multivariate analyses were performed to assess the effects on survival of the following factors: tumor maximum standardized uptake value (SUVmax) at baseline, preoperatively and at follow-up, decrease in tumor SUVmax, histological tumor type, grade, estrogen, progesterone, HER2/neu receptor status, and extent of disease at presentation including axillary nodal and distant metastases. Results By univariate analysis, survival was significantly associated with decrease in tumor SUVmax and tumor receptor status. Patients with decrease in tumor SUVmax had better survival (P = 0.02). Patients with a triple-negative tumor (P = 0.0006), a Her2/neu-negative tumor (P = 0.038) or an ER-negative tumor (P = 0.039) had worse survival. Multivariate analysis confirmed decrease in tumor SUVmax and triple-negative receptor status as significant predictors of survival. Every 10 % decrease in tumor SUVmax from baseline translated to a 15 % lower probability of death, and complete resolution of tumor FDG uptake translated to 80 % lower probability of death (P = 0.014). Patients with a triple-negative tumor had 4.11 times higher probability of death (P = 0.004). Conclusion Decrease in tumor SUVmax is an independent predictor of survival in patients with inflammatory breast cancer undergoing neoadjuvant chemotherapy. Further investigation with prospective studies is warranted to clarify its role in assessing response and altering therapy.
引用
收藏
页码:1809 / 1816
页数:8
相关论文
共 50 条
  • [31] Monitoring tumor response to neoadjuvant chemotherapy using MRI and 18F-FDG PET/CT in breast cancer subtypes
    Schmitz, Alexander M. Th.
    Teixeira, Suzana C.
    Pengel, Kenneth E.
    Loo, Claudette E.
    Vogel, Wouter V.
    Wesseling, Jelle
    Rutgers, Emiel J. Th.
    Olmos, Renato A. Valdes
    Sonke, Gabe S.
    Rodenhuis, Sjoerd
    Peeters, Marie Jeanne T. F. D. Vrancken
    Gilhuijs, Kenneth G. A.
    PLOS ONE, 2017, 12 (05):
  • [32] Study of 18F-FDG PET/CT imaging and neoadjuvant chemotherapy efficacy in different molecular subtypes of breast cancer
    Feng, Yan-lin
    Li, Wen
    JOURNAL OF NUCLEAR MEDICINE, 2015, 56 (03)
  • [33] Early monitoring of response to neoadjuvant chemotherapy in breast cancer with 18F-FDG PET/CT: defining a clinical aim
    Groheux, David
    Giacchetti, Sylvie
    Espie, Marc
    Rubello, Domenico
    Moretti, Jean-luc
    Hindie, Elif
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2011, 38 (03) : 419 - 425
  • [34] Efficacy of 18F-FDG PET/CT for Breast Cancer
    Mittra, E.
    Quon, A.
    Gambhir, S. S.
    Iagaru, A.
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2009, 36 : S176 - S176
  • [35] Predictive value of 18F-FDG PET/CT indices on extensive residual cancer burden in breast cancer patients treated with neoadjuvant chemotherapy
    Basoglu, Tugba
    Ozguven, Salih
    Ozkan, Huelya Sahin
    Cinar, Merve
    Kostek, Osman
    Demircan, Nazim Can
    Arikan, Rukiye
    Telli, Tugba Akin
    Ercelep, Ozlem
    Kaya, Handan
    Ones, Tunc
    Erdil, Tanju Yusuf
    Ugurlu, Mustafa Umit
    Dane, Faysal
    Yumuk, Perran Fulden
    REVISTA ESPANOLA DE MEDICINA NUCLEAR E IMAGEN MOLECULAR, 2022, 41 (03): : 171 - 178
  • [36] The utility of 18F-FDG PET/CT for monitoring of neoadjuvant therapy response in breast cancer
    Xing, W.
    Li, Q.
    Jiang, C.
    Chen, B.
    Sun, Y.
    BREAST, 2019, 44 : S76 - S77
  • [37] Prediction of the histopathological response to neoadjuvant chemotherapy by F-18-FDG PET/CT in patients with breast cancer
    Taki, Junichi
    Inokuchi, Masafumi
    Wakabayashi, Hiroshi
    Inaki, Anri
    Nakamura, Ayane
    Mochizuki, Takafumi
    Kinuya, Seigo
    JOURNAL OF NUCLEAR MEDICINE, 2010, 51
  • [38] Preoperative 18F-FDG PET/CT predicts disease-free survival in patients with primary invasive ductal breast cancer
    Jo, Ji Eun
    Kim, Jin You
    Lee, Suck Hong
    Kim, Suk
    Kang, Taewoo
    ACTA RADIOLOGICA, 2015, 56 (12) : 1463 - 1470
  • [39] Demonstration of the effectiveness of neoadjuvant chemotherapy and radiotherapy by 18F-FDG PET-CT and MRI in patients with colorectal cancer
    Gul, S. S.
    Rahatli, S.
    Guler, G.
    Sonmezgoz, F.
    Hasbek, Z.
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2016, 43 : S280 - S281
  • [40] Utility of 18F-FDG PET and CT to assess response to neoadjuvant chemotherapy.
    Chaft, Jamie E.
    Naidoo, Jarushka
    Dunphy, Mark
    Woo, Kaitlin
    Sima, Camelia S.
    Downey, Robert J.
    Travis, William D.
    Kris, Mark G.
    JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (15)