Seenu Vuthaluru, Sharma Ankit, Kumar Rakesh, Suhani Suhani, Prashanth Arun, Mathur Sandeep, Parshad Rajinder
Department of Surgical Disciplines, All India Institute of Medical Sciences, New Delhi, India.
Department of Nuclear Medicine, All India Institute of Medical Sciences, New Delhi, India.
World J Nucl Med. 2020 Jul 22;19(3):233-239. doi: 10.4103/wjnm.WJNM_71_19. eCollection 2020 Jul-Sep.
Estrogen receptor (ER) expression in breast cancer is routinely studied on immunohistochemistry (IHC) of tissue obtained from core biopsy or surgical specimen. Sampling error and heterogeneity of tumor may incorrectly label a breast tumor as ER negative, thus denying patient hormonal treatment. Molecular functional ER imaging can assess the in-vivo ER expression of primary tumor and metastases at sites inaccessible for biopsy and also track changes in expression over time. The aim was to study ER expression using 16α-F-fluoro-17β-estradiol or F-fluoroestradiol (F FES) positron emission tomography (PET) computed tomography (CT). Twenty-four biopsy-proven breast cancer patients consenting to participate in the study underwent FES PET CT. Standard uptake value (SUV) of maximum of 7 lesions/patient was analyzed, and tumor-to-background ratio was calculated for each lesion. Visual interpretation score was calculated for lesion on FES PET and correlated with the Allred score on IHC of tumor tissue samples for ER expression. The diagnostic indices of FES PET CT were assessed taking IHC as "gold standard." On FES PET CT, the mean SUV for ER+ tumors was 4.75, whereas the mean SUV for ER - tumors was 1.41. Using receiver operating characteristic curve, tumors with an SUV of ≥ 1.8 on FES PET could be considered as ER+. The overall accuracy of FES PET CT to detect ER expression was 91.66%, with two false negatives noted in this study. F-FES PET CT appears promising in evaluating ER expression in breast cancer. It is noninvasive and has potential to assess the in-vivo ER expression of the entire primary tumor and metastasis not amenable for biopsy.
乳腺癌中雌激素受体(ER)的表达通常通过对经粗针活检或手术标本获得的组织进行免疫组织化学(IHC)研究。肿瘤的取样误差和异质性可能会将乳腺肿瘤错误地标记为ER阴性,从而使患者无法接受激素治疗。分子功能ER成像可以评估原发性肿瘤和活检无法到达部位的转移灶的体内ER表达,还可以追踪表达随时间的变化。目的是使用16α-F-氟-17β-雌二醇或F-氟雌二醇(F-FES)正电子发射断层扫描(PET)计算机断层扫描(CT)研究ER表达。24例经活检证实同意参与研究的乳腺癌患者接受了FES PET CT检查。分析了每位患者最多7个病灶的标准摄取值(SUV),并计算每个病灶的肿瘤与背景比值。计算FES PET上病灶的视觉解释评分,并与肿瘤组织样本ER表达的IHC上的Allred评分相关。以IHC为“金标准”评估FES PET CT的诊断指标。在FES PET CT上,ER+肿瘤的平均SUV为4.75,而ER-肿瘤的平均SUV为1.41。使用受试者操作特征曲线,FES PET上SUV≥1.8的肿瘤可被视为ER+。FES PET CT检测ER表达的总体准确率为91.66%,本研究中发现两例假阴性。F-FES PET CT在评估乳腺癌ER表达方面似乎很有前景。它是非侵入性的,有潜力评估整个原发性肿瘤和无法活检的转移灶的体内ER表达。