Complete Metabolic Response on Interim 18F-Fluorodeoxyglucose Positron Emission Tomography/Computed Tomography to Predict Long-Term Survival in Patients with Breast Cancer Undergoing Neoadjuvant Chemotherapy

Author:

Chen Suyun12,Ibrahim Nuhad K.3,Yan Yuanqing4,Wong Stephen T.5,Wang Hui1,Wong Franklin C.2

Affiliation:

1. Department of Nuclear Medicine Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China

2. Department of Nuclear Medicine The University of Texas MD Anderson Cancer Center, Houston, Texas, USA

3. Department of Medical Oncology The University of Texas MD Anderson Cancer Center, Houston, Texas, USA

4. Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA

5. Department of System Medicine and Bioengineering Methodist Hospital Research Institution, Weill Cornell Medical College, Houston, Texas, USA

Abstract

Abstract Background This study aims to investigate the prognostic role of complete metabolic response (CMR) on interim 18F-fluorodeoxyglucose positron emission tomography/computed tomography (PET/CT) in patients with breast cancer (BC) receiving neoadjuvant chemotherapy (NAC) according to tumor subtypes and PET timing. Patients and Methods Eighty-six consecutive patients with stage II/III BC who received PET/CT during or following NAC were included. Time-dependent receiver operating characteristic analysis and Kaplan-Meier analysis were used to determine correlation between metabolic parameters and survival outcomes. Results The median follow-up duration was 71 months. Maximum standardized uptake value (SUVmax) on an interim PET/CT independently correlated with survival by multivariate analysis (overall survival [OS]: hazard ratio: 1.139, 95% confidence interval: 1.058–1.226, p = .001). By taking PET timing into account, best association of SUVmax with survival was obtained on PET after two to three cycles of NAC (area under the curve [AUC]: 0.941 at 1 year after initiation of NAC) and PET after four to five (AUC: 0.871 at 4 years), while PET after six to eight cycles of NAC had less prognostic value. CMR was obtained in 62% of patients (23/37) with estrogen receptor-positive (ER+)/human epidermal growth factor receptor 2-negative (HER2−) BC, in 48% (12/25) triple-negative BC (TNBC), and in 75% (18/24) HER2-positive (HER2+) tumors. Patients with CMR on an early-mid PET had 5-year OS rates of 92% for ER+/HER2− tumors and 80% for TNBC, respectively. Among HER2+ subtype, 89% patients (16/18) with CMR had no relapse. Conclusion CMR indicated a significantly better outcome in BC and may serve as a favorable imaging prognosticator.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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