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Poster Display session 2

2632 - Ring-like uptake appearance on dedicated breast positron emission tomography before chemotherapy predicts outcome of neoadjuvant chemotherapy in breast cancer


29 Sep 2019


Poster Display session 2


Tumour Site

Breast Cancer


Norio Masumoto


Annals of Oncology (2019) 30 (suppl_5): v55-v98. 10.1093/annonc/mdz240


N. Masumoto1, T. Kadoya2, M. Nishina3, Y. Kimura4, A. Amioka4, T. Itagaki4, S. Sasada4, A. Emi4, M. Okada4

Author affiliations

  • 1 Surgical Oncology, Hiroshima University, 734-0037 - Hiroshima/JP
  • 2 Surgical Oncology, Institute of Biomedical & Health Sciences, Hiroshima University, 734-8551 - Hiroshima/JP
  • 3 Surgical Oncology, Hiroshima University, 734-8551 - Hiroshima/JP
  • 4 Surgical Oncology, Hiroshima University, Hiroshima/JP


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Abstract 2632


Dedicated breast positron emission tomography (DbPET) with 18F-fluorodeoxyglucose (FDG) can detect intratumoral heterogeneity. In a previous study, we proved that intratumoral heterogeneous distribution of FDG on DbPET is significantly related to a high nuclear grade and high Ki-67 proliferation index; we also proved that DbPET is useful for predicting residual breast tumors after neoadjuvant chemotherapy (NAC). This study included patients with breast cancer who exhibited a ring-like uptake without central FDG accumulation on DbPET and aimed to evaluate whether the uptake can predict the effects of NAC in patients with breast cancer.


The study included 83 consecutive patients with breast cancer who subsequently underwent DbPET and NAC between August 2016 and March 2019 and evaluated the relationship between pathological response to NAC and clinicopathologic factors (clinical T1: n = 14; clinical N0: n = 33; nuclear grade 1 or 2: n = 22; Ki67 ≥ 20: n = 78; ER positive: n = 52; and HER-2 positive: n = 32), such as intratumoral heterogeneous distribution of FDG (positive: n = 54) and ring-like uptake without central FDG accumulation (positive: n = 11) on DbPET images.


Surgical pathological findings obtained after the NAC indicated pathological complete response (pCR) and non-pCR in 32 (38.6%) and 51 (61.4%) patients, respectively. For all the patients, significant predictors for pCR were identified in univariate analyses (clinical T: odds ratio = 3.60, p = 0.03; clinical N: odds ratio = 2.48, p = 0.049; HER-2 overexpression: odds ratio = 2.72, p = 0.03; and ring-like uptake: odds ratio = 5.33, p = 0.01) and multivariate analyses (HER-2 overexpression: odds ratio = 3.29, p = 0.03; ring-like uptake: odds ratio = 17.6, p = 0.0006) (Table).Table:

279P Univariate and multivariate logistic analysis of significant predictive clinicopathological factors for pCR

CharacteristicUnivariate logistic analysisMultivariate logistic analysis
Age, <50 v ≥ 501.380.57-3.380.481.970.65-5.980.23
Clinical T, T1 v T2- T43.601.11-
Clinical N, Negative v Positive2.481.00-6.280.0492.860.97-8.420.06
Nuclear Grade, 3 v 1-21.490.54-4.380.451.650.41-6.700.48
Ki67, ≥20 v < 202.640.37-52.80.361.340.11-16.50.82
ER, Negative v Positive1.250.50-3.120.631.050.33-3.340.93
HER-2, Positive v Negative2.721.09-6.940.033.29 1.11-9.730.03
Intratumoral heterogenity, Positive v Negative1.500.59-3.780.391.690.43-6.570.45
Ring-like uptake, Positive v Negative5.331.40-26.10.0117.62.27-136.20.006


Ring-like uptake on DbPET provides predictive value for evaluating pCR to NAC in patients with breast cancer and might inform therapeutic decisions.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.


Has not received any funding.


All authors have declared no conflicts of interest.

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