Physicians may soon have a new way to measure the efficacy or failure of hormone therapy for breast cancer patients, according to new research published in the February issue of The Journal of Nuclear Medicine. Researchers report that positron emission tomography (PET) imaging with 18F-fluorofuranyl norprogesterone (18F-FFNP) has been found to successfully measure changes in progesterone receptor (PR) levels resulting from a short-course estrogen treatment, also known as an estradiol challenge.
Estrogen-receptor (ER)-positive breast cancer is the most common class of breast cancer, affecting nearly 70 percent of patients. By participating in an estradiol challenge, physicians can determine the likelihood of the potential benefit of hormonal therapies targeting ER for individual patients. Many hormone therapies interfere with the ability of estrogen to regulate the expression of PR protein; which is more pronounced in the presence of estrogen.
As such, several PET tracers are developing to monitor and analyze changes in the PR level during therapy. “Typically, anatomic size and proliferation biomarkers are analyze to determine endocrine sensitivity,” said Amy M. Fowler, MD, Ph.D., assistant professor, Section of Breast Imaging, Department of Radiology, University of Wisconsin-Madison. “However, non-invasive detection of changes in PR expression with 18F-FFNP during an estradiol challenge may be an earlier indicator of the effectiveness of specific hormone therapy.”
Breast cancer cells
In this study, T47D human breast cancer cells (cells with estrogen and progesterone receptors, but without human epidermal growth factor receptor-2) and mice bearing T47D tumor xenografts are treating with estrogen to increase PR expression. The cells and mice are imaging with 18F-FFNP, and assays are conducting for cell uptake and tissue biodistribution.
To investigate the separate role of PR-A and PR-B isoforms on the overall 18F-FFNP binding; triple-negative MDA-MB-231 breast cancer cells are engineere to express either PR-A or PR-B. In vitro 18F-FFNP binding is measuring by saturation and competitive binding assays; while in vivo uptake is measuring with PET imaging.
In T47D cells treate with estrogen, an increase in 18F-FFNP uptake is measuring at 48 hours after treatment; in mice with T47D tumor xenografts, increase uptake was seen at 48 and 72 hours after treatment. This increase in 18F-FFNP uptake also correlated with an increase in PR protein expression and proliferation.
Results showed that there was no significant preferential 18F-FFNP binding or uptake by PR-A versus PR-B in PR isoform cell lines or tumor xenografts. “This is an important finding given the variability of PR isoform expression observed in breast cancer patients,” stated Fowler.
She continued; “Validation of PR imaging as a biomarker of endocrine sensitivity in patients before and after estradiol challenge could provide new opportunities in the field of molecular imaging and nuclear medicine for breast cancer imaging. Improved methods for testing endocrine sensitivity in patients could better inform decisions for optimal individualized ER-positive breast cancer therapy; potentially reducing morbidity and mortality.”