Early metabolic response using FDG PET/CT and molecular phenotypes of breast cancer treated with neoadjuvant chemotherapy

被引:58
|
作者
Keam, Bhumsuk [1 ,2 ]
Im, Seock-Ah [1 ,2 ]
Koh, Youngil [1 ]
Han, Sae-Won [1 ,2 ]
Oh, Do-Youn [1 ,2 ]
Cho, Nariya [4 ]
Kim, Jee Hyun [1 ,2 ]
Han, Wonshik [5 ]
Kang, Keon Wook [2 ,3 ]
Moon, Woo Kyung [4 ]
Kim, Tae-You [1 ,2 ]
Park, In Ae [6 ]
Noh, Dong-Young [5 ]
Chung, June-Key [2 ,3 ]
Bang, Yung-Jue [1 ,2 ]
机构
[1] Seoul Natl Univ, Coll Med, Dept Internal Med, Seoul 151, South Korea
[2] Seoul Natl Univ, Coll Med, Canc Res Inst, Seoul, South Korea
[3] Seoul Natl Univ, Coll Med, Dept Nucl Med, Seoul, South Korea
[4] Seoul Natl Univ, Coll Med, Dept Radiol, Seoul, South Korea
[5] Seoul Natl Univ, Coll Med, Dept Surg, Seoul, South Korea
[6] Seoul Natl Univ, Coll Med, Dept Pathol, Seoul 151, South Korea
来源
BMC CANCER | 2011年 / 11卷
基金
新加坡国家研究基金会;
关键词
FDG PET; breast cancer; neoadjuvant chemotherapy; molecular phenotype; POSITRON-EMISSION-TOMOGRAPHY; PATHOLOGICAL RESPONSE; F-18; FLUORODEOXYGLUCOSE; PRIMARY TUMOR; BLOOD-FLOW; PHASE-II; STAGE-II; IN-SITU; DOXORUBICIN; GUIDELINES;
D O I
10.1186/1471-2407-11-452
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: This study was aimed 1) to investigate the predictive value of FDG PET/CT (fluorine-18 fluorodeoxyglucose positron emission tomography/computed tomography) for histopathologic response and 2) to explore the results of FDG PET/CT by molecular phenotypes of breast cancer patients who received neoadjuvant chemotherapy. Methods: Seventy-eight stage II or III breast cancer patients who received neoadjuvant docetaxel/doxorubicin chemotherapy were enrolled in this study. FDG PET/CTs were acquired before chemotherapy and after the first cycle of chemotherapy for evaluating early metabolic response. Results: The mean pre- and post-chemotherapy standard uptake value (SUV) were 7.5 and 3.9, respectively. The early metabolic response provided by FDG PET/CT after one cycle of neoadjuvant chemotherapy was correlated with the histopathologic response after completion of neoadjuvant chemotherapy (P = 0.002). Sensitivity and negative predictive value were 85.7% and 95.1%, respectively. The estrogen receptor negative phenotype had a higher pre-chemotherapy SUV (8.6 vs. 6.4, P = 0.047) and percent change in SUV (48% vs. 30%, P = 0.038). In triple negative breast cancer (TNBC), the pre-chemotherapy SUV was higher than in non-TNBC (9.8 vs. 6.4, P = 0.008). Conclusions: The early metabolic response using FDG PET/CT could have a predictive value for the assessment of histopathologic non-response of stage II/III breast cancer treated with neoadjuvant chemotherapy. Our findings suggest that the initial SUV and the decline in SUV differed based on the molecular phenotype.
引用
收藏
页数:9
相关论文
共 50 条
  • [41] Tumor metabolism with 18F-FDG PET/CT predicts final neoadjuvant chemotherapy response in breast cancer
    Garcia Vicente, Ana Maria
    Soriano, Angel
    Leon Martin, Alberto
    Cruz Mora, Miguel Angel
    Munoz Sanchez, Maria del Mar
    Relea Calatayud, Fernanda
    JOURNAL OF NUCLEAR MEDICINE, 2014, 55
  • [42] Role of F-18 FDG PET/CT in Predicting Response to Neoadjuvant Chemotherapy in Invasive Ductal Breast Cancer
    Sengoz, Tarik
    Karakaya, Yeliz Arman
    Gueltekin, Aziz
    Yilmaz, Sevda
    Erdem, Ergun
    Taskoylu, Burcu Yapar
    Kesen, Zehra
    Yaylali, Olga
    Yuksel, Dogangun
    EUROPEAN JOURNAL OF BREAST HEALTH, 2023, 19 (02) : 159 - 165
  • [43] Relevance of Breast Cancer Subtypes in Response Monitoring with 18F-FDG PET/CT During Neoadjuvant Chemotherapy
    Koolen, B. B.
    Pengel, K. E.
    Wesseling, J.
    Vogel, W. V.
    Peeters, M. Vrancken
    Gilhuijs, K. G.
    Rodenhuis, S.
    Rutgers, E. J.
    Olmos, R. A. Valdes
    EUROPEAN JOURNAL OF CANCER, 2012, 48 : S42 - S42
  • [44] Feasibility of FDG PET/CT to monitor the response of axillary lymph node metastases to neoadjuvant chemotherapy in breast cancer patients
    Marieke E. Straver
    Tjeerd S. Aukema
    Renato A. Valdes Olmos
    Emiel J. T. Rutgers
    Kenneth G. A. Gilhuijs
    Margaret E. Schot
    Wouter V. Vogel
    Marie-Jeanne T. F. D. Vrancken Peeters
    European Journal of Nuclear Medicine and Molecular Imaging, 2010, 37 : 1069 - 1076
  • [45] Glycolytic activity with 18F-FDG PET/CT predicts final neoadjuvant chemotherapy response in breast cancer
    Garcia Vicente, Ana Maria
    Cruz Mora, Miguel Angel
    Leon Martin, Antonio Alberto
    Munoz Sanchez, Maria del Mar
    Relea Calatayud, Fernanda
    Van Gomez Lopez, Ober
    Espinosa Aunion, Ruth
    Gonzalez Ageitos, Ana
    Soriano Castrejon, Angel
    TUMOR BIOLOGY, 2014, 35 (11) : 11613 - 11620
  • [46] Feasibility of FDG PET/CT to monitor the response of axillary lymph node metastases to neoadjuvant chemotherapy in breast cancer patients
    Straver, Marieke E.
    Aukema, Tjeerd S.
    Olmos, Renato A. Valdes
    Rutgers, Emiel J. T.
    Gilhuijs, Kenneth G. A.
    Schot, Margaret E.
    Vogel, Wouter V.
    Peeters, Marie-Jeanne T. F. D. Vrancken
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2010, 37 (06) : 1069 - 1076
  • [47] MRI phenotypes predict response and recurrence in locallyadvanced breast cancer treated with neoadjuvant chemotherapy
    Yu, E
    Gibbs, J
    Au, A
    Chew, K
    Hylton, N
    Esserman, L
    Hwang, S
    Ewing, C
    Rugo, H
    Park, J
    Tripathy, D
    JOURNAL OF INVESTIGATIVE MEDICINE, 2003, 51 (06) : 340 - 340
  • [48] 18F-FDG PET/CT and PET for evaluation of pathological response to neoadjuvant chemotherapy in breast cancer: a meta-analysis
    Cheng, Xu
    Li, Yongjun
    Liu, Biao
    Xu, Zhaoqiang
    Bao, Lihua
    Wang, Jie
    ACTA RADIOLOGICA, 2012, 53 (06) : 615 - 627
  • [49] 18F-FDG PET/CT and PET for evaluation of pathological response to neoadjuvant chemotherapy in breast cancer: A meta-analysis
    Cheng, Xu
    Li, Yongjun
    Liu, Biao
    JOURNAL OF NUCLEAR MEDICINE, 2012, 53
  • [50] Early Predictive Value of Non-response to Docetaxel in Neoadjuvant Chemotherapy in Breast Cancer Using 18F-FDG-PET
    Hirakata, Tomoko
    Yanagita, Yasuhiro
    Fujisawa, Tomomi
    Fujii, Takaaki
    Kinoshita, Teruhiko
    Horikoshi, Hiroyuki
    Oya, Nariyuki
    Akiyoshi, Tsukasa
    Iijima, Misa
    Miyamoto, Takeshi
    Kuwano, Hiroyuki
    ANTICANCER RESEARCH, 2014, 34 (1A) : 221 - 226