Boers Jorianne, Eisses Bertha, Zwager Mieke C, van Geel Jasper J L, Bensch Frederike, de Vries Erik F J, Hospers Geke A P, Glaudemans Andor W J M, Brouwers Adrienne H, den Dekker Martijn A M, Elias Sjoerd G, Kuip Evelien J M, van Herpen Carla M L, Jager Agnes, van der Veldt Astrid A M, Oprea-Lager Daniela E, de Vries Elisabeth G E, van der Vegt Bert, Menke-van der Houven van Oordt Willemien C, Schröder Carolina P
Department of Medical Oncology, University Medical Center Groningen, University of Groningen, 9713 Groningen, The Netherlands.
Department of Pathology, University Medical Center Groningen, University of Groningen, 9713 Groningen, The Netherlands.
Diagnostics (Basel). 2024 Feb 14;14(4):416. doi: 10.3390/diagnostics14040416.
In metastatic breast cancer (MBC), [F]fluorodeoxyglucose positron emission tomography/computed tomography ([F]FDG-PET/CT) can be used for staging. We evaluated the correlation between BC histopathological characteristics and [F]FDG uptake in corresponding metastases.
Patients with non-rapidly progressive MBC of all subtypes prospectively underwent a baseline histological metastasis biopsy and [F]FDG-PET. Biopsies were assessed for estrogen, progesterone, and human epidermal growth factor receptor 2 (ER, PR, HER2); Ki-67; and histological subtype. [F]FDG uptake was expressed as maximum standardized uptake value (SUV) and results were expressed as geometric means.
Of 200 patients, 188 had evaluable metastasis biopsies, and 182 of these contained tumor. HER2 positivity and Ki-67 ≥ 20% were correlated with higher [F]FDG uptake (estimated geometric mean SUV 10.0 and 8.8, respectively; = 0.0064 and = 0.014). [F]FDG uptake was lowest in ER-positive/HER2-negative BC and highest in HER2-positive BC (geometric mean SUV 6.8 and 10.0, respectively; = 0.0058). Although [F]FDG uptake was lower in invasive lobular carcinoma ( = 31) than invasive carcinoma NST ( = 146) (estimated geometric mean SUV 5.8 versus 7.8; = 0.014), the metastasis detection rate was similar.
[F]FDG-PET is a powerful tool to detect metastases, including invasive lobular carcinoma. Although BC histopathological characteristics are related to [F]FDG uptake, [F]FDG-PET and biopsy remain complementary in MBC staging (NCT01957332).
在转移性乳腺癌(MBC)中,[F]氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描([F]FDG-PET/CT)可用于分期。我们评估了乳腺癌组织病理学特征与相应转移灶中[F]FDG摄取之间的相关性。
所有亚型的非快速进展性MBC患者前瞻性地接受了基线组织学转移灶活检和[F]FDG-PET检查。对活检组织进行雌激素、孕激素和人表皮生长因子受体2(ER、PR、HER2);Ki-67;以及组织学亚型的评估。[F]FDG摄取以最大标准化摄取值(SUV)表示,结果以几何平均数表示。
200例患者中,188例有可评估的转移灶活检,其中182例含有肿瘤。HER2阳性和Ki-67≥20%与较高的[F]FDG摄取相关(估计几何平均SUV分别为10.0和8.8;P = 0.0064和P = 0.014)。[F]FDG摄取在ER阳性/HER2阴性乳腺癌中最低,在HER2阳性乳腺癌中最高(几何平均SUV分别为6.8和10.0;P = 0.0058)。尽管浸润性小叶癌(n = 31)的[F]FDG摄取低于浸润性非特殊类型癌(n = 146)(估计几何平均SUV为5.8对7.8;P = 0.014),但转移灶检出率相似。
[F]FDG-PET是检测转移灶的有力工具,包括浸润性小叶癌。尽管乳腺癌组织病理学特征与[F]FDG摄取有关,但在MBC分期中[F]FDG-PET和活检仍具有互补性(NCT01957332)。