Correlation between Histopathological Prognostic Tumor Characteristics and [18F]FDG Uptake in Corresponding Metastases in Newly Diagnosed Metastatic Breast Cancer

Author:

Boers Jorianne1,Eisses Bertha1ORCID,Zwager Mieke C.2,van Geel Jasper J. L.1ORCID,Bensch Frederike1,de Vries Erik F. J.3ORCID,Hospers Geke A. P.1,Glaudemans Andor W. J. M.3ORCID,Brouwers Adrienne H.3ORCID,den Dekker Martijn A. M.4,Elias Sjoerd G.5,Kuip Evelien J. M.6,van Herpen Carla M. L.6,Jager Agnes7,van der Veldt Astrid A. M.7ORCID,Oprea-Lager Daniela E.8,de Vries Elisabeth G. E.1,van der Vegt Bert2ORCID,Menke-van der Houven van Oordt Willemien C.9ORCID,Schröder Carolina P.110

Affiliation:

1. Department of Medical Oncology, University Medical Center Groningen, University of Groningen, 9713 Groningen, The Netherlands

2. Department of Pathology, University Medical Center Groningen, University of Groningen, 9713 Groningen, The Netherlands

3. Department of Nuclear Medicine and Molecular Imaging, University Medical Center Groningen, University of Groningen, 9713 Groningen, The Netherlands

4. Department of Radiology, University Medical Center Groningen, University of Groningen, 9713 Groningen, The Netherlands

5. Department of Epidemiology, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, 3584 Utrecht, The Netherlands

6. Department of Medical Oncology, Radboud Medical Center, 6500 Nijmegen, The Netherlands

7. Department of Medical Oncology, Erasmus MC Cancer Institute, 3015 Rotterdam, The Netherlands

8. Department of Radiology and Nuclear Medicine, Amsterdam University Medical Center, Location VU University Medical Center, 1081 Amsterdam, The Netherlands

9. Department of Medical Oncology, Amsterdam University Medical Center, Location VU University Medical Center, 1081 Amsterdam, The Netherlands

10. Department of Medical Oncology, Dutch Cancer Institute, 1066 Amsterdam, The Netherlands

Abstract

Background: In metastatic breast cancer (MBC), [18F]fluorodeoxyglucose positron emission tomography/computed tomography ([18F]FDG-PET/CT) can be used for staging. We evaluated the correlation between BC histopathological characteristics and [18F]FDG uptake in corresponding metastases. Patients and Methods: Patients with non-rapidly progressive MBC of all subtypes prospectively underwent a baseline histological metastasis biopsy and [18F]FDG-PET. Biopsies were assessed for estrogen, progesterone, and human epidermal growth factor receptor 2 (ER, PR, HER2); Ki-67; and histological subtype. [18F]FDG uptake was expressed as maximum standardized uptake value (SUVmax) and results were expressed as geometric means. Results: Of 200 patients, 188 had evaluable metastasis biopsies, and 182 of these contained tumor. HER2 positivity and Ki-67 ≥ 20% were correlated with higher [18F]FDG uptake (estimated geometric mean SUVmax 10.0 and 8.8, respectively; p = 0.0064 and p = 0.014). [18F]FDG uptake was lowest in ER-positive/HER2-negative BC and highest in HER2-positive BC (geometric mean SUVmax 6.8 and 10.0, respectively; p = 0.0058). Although [18F]FDG uptake was lower in invasive lobular carcinoma (n = 31) than invasive carcinoma NST (n = 146) (estimated geometric mean SUVmax 5.8 versus 7.8; p = 0.014), the metastasis detection rate was similar. Conclusions: [18F]FDG-PET is a powerful tool to detect metastases, including invasive lobular carcinoma. Although BC histopathological characteristics are related to [18F]FDG uptake, [18F]FDG-PET and biopsy remain complementary in MBC staging (NCT01957332).

Funder

Dutch Cancer Society

Publisher

MDPI AG

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