18F-Fluoroestradiol Tumor Uptake Is Influenced by Structural Components in Breast Cancer.


Journal

Clinical nuclear medicine
ISSN: 1536-0229
Titre abrégé: Clin Nucl Med
Pays: United States
ID NLM: 7611109

Informations de publication

Date de publication:
01 Nov 2021
Historique:
pubmed: 29 7 2021
medline: 16 10 2021
entrez: 28 7 2021
Statut: ppublish

Résumé

Estrogen receptor (ER) is expressed in the majority of invasive breast cancer and is an important prognostic indicator. The tumor stroma also plays an important role in disease progression. This study evaluated the effect of stromal components on 16α-[18F]-fluoro-17β-estradiol (18F-FES) uptake in breast cancer and proposed a partial-volume correction method for 18F-FES PET based on histopathological analyses. Fifteen patients with biopsy-confirmed breast cancer underwent preoperative 18F-FES PET. Estrogen receptor expression in biopsy specimens was assayed by immunohistochemistry, cellular components in surgical specimens were measured using hematoxylin-eosin staining, and nuclear components in surgical and biopsy specimens were measured using Azan-Mallory staining. The relationship between 18F-FES SUV of the primary tumor and histopathological findings including ER expression, the Allred score, ER-positive cellular component ratio, and ER-positive nuclear component ratio (NCR) was examined. The relationship between stroma-free 18F-FES SUV and ER expression was also examined. 18F-FES uptake was not significantly positively correlated with ER expression (r = 0.44, P = 0.10). 18F-FES uptake was significantly correlated with the Allred score, ER-positive cellular component ratio, and ER-positive NCR in surgical specimens (ρ = 0.60, P = 0.02; r = 0.55, P = 0.03; and r = 0.65, P = 0.01, respectively). 18F-FES uptake was predominantly correlated with ER-positive NCR in biopsy specimens (r = 0.84, P < 0.001). Stroma-free 18F-FES SUV was significantly correlated with ER expression (r = 0.78, P < 0.01). 18F-FES PET predominantly demonstrates the level of ER expression in breast cancer cell nucleus. Although tumor 18F-FES uptake is affected by the degree of stromal components, the partial volume effect on the uptake can be corrected by stroma-volume fraction in Azan-Mallory staining.

Identifiants

pubmed: 34319950
doi: 10.1097/RLU.0000000000003835
pii: 00003072-202111000-00003
doi:

Substances chimiques

Receptors, Estrogen 0
Estradiol 4TI98Z838E

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

884-889

Informations de copyright

Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest and sources of funding: This study was partly funded by the Takeda Science Foundation. The authors declare that they have no potential conflicts of interest.

Références

Tryfonidis K, Zardavas D, Katzenellenbogen BS, et al. Endocrine treatment in breast cancer: cure, resistance and beyond. Cancer Treat Rev . 2016;50:68–81.
McGuire AH, Dehdashti F, Siegel BA, et al. Positron tomographic assessment of 16α-[ 18 F] fluoro-17β-estradiol uptake in metastatic breast carcinoma. J Nucl Med . 1991;32:1526–1531.
Linden HM, Stekhova SA, Link JM, et al. Quantitative fluoroestradiol positron emission tomography imaging predicts response to endocrine treatment in breast cancer. J Clin Oncol . 2006;24:2793–2799.
Linden HM, Kurland BF, Peterson LM, et al. Fluoroestradiol positron emission tomography reveals differences in pharmacodynamics of aromatase inhibitors, tamoxifen, and fulvestrant in patients with metastatic breast cancer. Clin Cancer Res . 2011;17:4799–4805.
CERIANNA™ (fluoroestradiol F 18) Injection, for intravenous use Initial U.S. Approval, May 20, 2020.
Mintun MA, Welch MJ, Siegel BA, et al. Breast cancer: PET imaging of estrogen receptors. Radiology . 1988;169:45–48.
Peterson LM, Mankoff DA, Lawton T, et al. Quantitative imaging of estrogen receptor expression in breast cancer with PET and 18 F-fluoroestradiol. J Nucl Med . 2008;49:367–374.
de Kruijf EM, van Nes JG, van de Velde CJ, et al. Tumor-stroma ratio in the primary tumor is a prognostic factor in early breast cancer patients, especially in triple-negative carcinoma patients. Breast Cancer Res Treat . 2011;125:687–696.
Loktev A, Lindner T, Mier W, et al. A tumor-imaging method targeting cancer-associated fibroblasts. J Nucl Med . 2018;59:1423–1429.
Mankoff DA, Tewson TJ, Eary JF. Analysis of blood clearance and labeled metabolites for the estrogen receptor tracer [F-18]-16α-fluoroestradiol. Nucl Med Biol . 1997;24:341–348.
Evangelista L, Guarneri V, Conte PF. 18 F-Fluoroestradiol positron emission tomography in breast cancer patients: systematic review of the literature & meta-analysis. Curr Radiopharm . 2016;9:244–257.
Allison KH, Hammond MEH, Dowsett M, et al. Estrogen and progesterone receptor testing in breast cancer: ASCO/CAP guideline update. J Clin Oncol . 2020;38:1346–1366.
Allred DC, Harvey JM, Berardo M, et al. Prognostic and predictive factors in breast cancer by immunohistochemical analysis. Mod Pathol . 1998;11:155–168.
Mesker WE, Junggeburt JM, Szuhai K, et al. The carcinoma-stromal ratio of colon carcinoma is an independent factor for survival compared to lymph node status and tumor stage. Cell Oncol . 2007;29:387–398.
Levin ER. Extranuclear steroid receptors are essential for steroid hormone actions. Annu Rev Med . 2015;66:271–280.
Aurilio G, Disalvatore D, Pruneri G, et al. A meta-analysis of oestrogen receptor, progesterone receptor and human epidermal growth factor receptor 2 discordance between primary breast cancer and metastases. Eur J Cancer . 2014;50:277–289.
Chae SY, Ahn SH, Kim SB, et al. Diagnostic accuracy and safety of 16α-[ 18 F]fluoro-17β-oestradiol PET-CT for the assessment of oestrogen receptor status in recurrent or metastatic lesions in patients with breast cancer: a prospective cohort study. Lancet Oncol . 2019;20:546–555.
Kurland BF, Wiggins JR, Coche A, et al. Whole-body characterization of estrogen receptor status in metastatic breast cancer with 16α- 18 F-Fluoro-17β-estradiol positron emission tomography: meta-analysis and recommendations for integration into clinical applications. Oncologist . 2020;25:835–844.
Elledge RM, Green S, Pugh R, et al. Estrogen receptor (ER) and progesterone receptor (PgR), by ligand-binding assay compared with ER, PgR and pS2, by immuno-histochemistry in predicting response to tamoxifen in metastatic breast cancer: a Southwest Oncology Group Study. Int J Cancer . 2000;89:111–117.

Auteurs

Mizuho Takahashi (M)

From the First Department of Surgery, Faculty of Medical Sciences.

Hiroyuki Maeda (H)

From the First Department of Surgery, Faculty of Medical Sciences.

Tetsuya Tsujikawa (T)

Biomedical Imaging Research Center, University of Fukui.

Hiroko Kono (H)

From the First Department of Surgery, Faculty of Medical Sciences.

Tetsuya Mori (T)

Biomedical Imaging Research Center, University of Fukui.

Yasushi Kiyono (Y)

Biomedical Imaging Research Center, University of Fukui.

Hidehiko Okazawa (H)

Biomedical Imaging Research Center, University of Fukui.

Sakon Noriki (S)

Faculty of Nursing and Social Welfare Science, Fukui Prefectural University.

Yoshiaki Imamura (Y)

Division of Surgical Pathology, University of Fukui Hospital, Fukui, Japan.

Takanori Goi (T)

From the First Department of Surgery, Faculty of Medical Sciences.

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