18F-fluoroestradiol PET: current status and potential future clinical applications

GJ Liao, AS Clark, EK Schubert… - Journal of Nuclear …, 2016 - Soc Nuclear Med
Estrogen receptor (ER) expression in breast cancer is associated with a more favorable
prognosis and is necessary for a response to endocrine therapies. Traditionally, ER …

Targeting the androgen receptor in breast cancer

KM Chia, M O'Brien, M Brown, E Lim - Current oncology reports, 2015 - Springer
The androgen receptor (AR) is expressed in the majority of breast cancer and across the
three main breast cancer subtypes. Historically, the oncogenic role of AR has best been …

Estrogen Receptor Binding (18F-FES PET) and Glycolytic Activity (18F-FDG PET) Predict Progression-Free Survival on Endocrine Therapy in Patients with ER+ …

BF Kurland, LM Peterson, JH Lee, EK Schubert… - Clinical Cancer …, 2017 - AACR
Abstract Purpose: 18F-fluoroestradiol (FES) PET scans measure regional estrogen binding,
and 18F-fluorodeoxyglucose (FDG) PET measures tumor glycolytic activity. We examined …

18F-Fluoroestradiol PET/CT Measurement of Estrogen Receptor Suppression during a Phase I Trial of the Novel Estrogen Receptor-Targeted Therapeutic GDC-0810 …

Y Wang, KL Ayres, DA Goldman, MN Dickler… - Clinical Cancer …, 2017 - AACR
Abstract Purpose: Evaluate 18F-fluoroestradiol (FES) PET/CT as a biomarker of estrogen
receptor (ER) occupancy and/or downregulation during phase I dose escalation of the novel …

The quest for improving the management of breast cancer by functional imaging: The discovery and development of 16α-[18F] fluoroestradiol (FES), a PET radiotracer …

JA Katzenellenbogen - Nuclear medicine and biology, 2021 - Elsevier
Abstract Introduction 16α-[18 F] Fluoroestradiol (FES), a PET radiotracer for the estrogen
receptor (ER) in breast cancer, was the first receptor-targeted PET radiotracer for oncology …

G1T48, an oral selective estrogen receptor degrader, and the CDK4/6 inhibitor lerociclib inhibit tumor growth in animal models of endocrine-resistant breast cancer

KJ Andreano, SE Wardell, JG Baker… - Breast cancer research …, 2020 - Springer
Purpose The combination of targeting the CDK4/6 and estrogen receptor (ER) signaling
pathways with palbociclib and fulvestrant is a proven therapeutic strategy for the treatment of …

The Predictive Value of Early Changes in 18F‐Fluoroestradiol Positron Emission Tomography/Computed Tomography During Fulvestrant 500 mg Therapy in Patients …

M He, C Liu, Q Shi, Y Sun, Y Zhang, X Xu… - The …, 2020 - academic.oup.com
Background The aim of this study was to investigate the predictive value of early changes in
18F‐fluoroestradiol (FES) positron emission tomography (PET)/computed tomography (CT) …

Optimization of an indazole series of selective estrogen receptor degraders: Tumor regression in a tamoxifen-resistant breast cancer xenograft

SP Govek, JY Nagasawa, KL Douglas, AG Lai… - Bioorganic & medicinal …, 2015 - Elsevier
Selective estrogen receptor degraders (SERDs) have shown promise for the treatment of
ER+ breast cancer. Disclosed herein is the continued optimization of our indazole series of …

Recent advances in imaging steroid hormone receptors in breast cancer

M Kumar, K Salem, AJ Tevaarwerk… - Journal of Nuclear …, 2020 - Soc Nuclear Med
Estrogen receptor (ER) and progesterone receptor (PR) are important prognostic and
predictive biomarkers in breast cancer. PET using ER-and PR-specific radioligands enables …

PET imaging agents (FES, FFNP, and FDHT) for estrogen, androgen, and progesterone receptors to improve management of breast and prostate cancers by …

JA Katzenellenbogen - Cancers, 2020 - mdpi.com
Many breast and prostate cancers are driven by the action of steroid hormones on their
cognate receptors in primary tumors and in metastases, and endocrine therapies that inhibit …