Hormone therapy commonly is given as a targeted treatment for women whose cancer cells carry receptors for oestrogen.
But the therapy only works for about half of all patients. Until now, there hasn’t been a good way to reliably predict who will benefit and who will not.
Researchers at Washington University School of Medicine in St. Louis, USA, have shown they can distinguish patients likely or unlikely to benefit from hormone therapy using an imaging test that measures the function of the oestrogen receptors in their cancer cells.
In a small phase 2 clinical trial, the researchers showed that the cancers of all patients with working oestrogen receptors remained stable or improved on hormone therapy, and progressed in all women with nonfunctional oestrogen receptors.
The findings, published in Nature Communications, could help doctors choose among treatment options and reduce the chances that women would receive a therapy unlikely to help.
“If breast cancer in a patient is oestrogen receptor-positive, doctors will usually recommend hormone therapy even though they know it will only work for slightly more than half the patients,” said senior author Farrokh Dehdashti, MD, the Drs. Barry A. and Marilyn J. Siegel Professor of Radiology at Mallinckrodt Institute of Radiology (MIR).
“When hormone therapy works, it’s typically quite effective, and it has milder side effects than some other therapies, and that’s why oncologists and patients want to try it first. But we need to narrow down who is likely to benefit, and there really hasn’t been a reliable test to accomplish that.”
Approximately four out of five breast cancers – some 250,000 per year in the United States – are labeled “oestrogen receptor-positive,” meaning that the cancer cells carry oestrogen receptors and the tumour grows in response to the naturally occurring hormone oestrogen. Hormone therapy is designed to stop the effects of oestrogen on the tumour.
A variety of drugs can be prescribed as hormone therapy, and doctors choose a treatment regimen depending on the patient and the specifics of that person’s disease. Aromatase inhibitors prevent the body from making oestrogen and are usually the first treatment chosen for hormone therapy.
Fulvestrant blocks the oestrogen receptor on cancer cells. These drugs usually are given to postmenopausal women. Pre-menopausal women often are given different hormone therapies because their ovaries still are producing large amounts of oestrogen.
Doctors have long suspected that the difference between women who respond to hormone therapy and those who don’t comes down to whether the oestrogen receptors on their cancer cells are working properly. If the receptors are present but nonfunctional, targeting them is unlikely to have much effect.
Dehdashti and colleagues, including co-authors Barry A. Siegel, MD, a professor of radiology, set about measuring the functionality of oestrogen receptors by taking advantage of a link between the oestrogen receptor and a receptor for another hormone: progesterone. When oestrogen receptors are stimulated, cells respond by increasing the number of progesterone receptor molecules on their surfaces.
Co-author John Katzenellenbogen, PhD, a chemist at the University of Illinois, designed an imaging agent to probe the number of progesterone receptors on the surface of cancer cells, in collaboration with the late Michael Welch, PhD, then a professor of radiology at Washington University.
The compound, 21-[18F] fluorofuranylnorprogesterone (FFNP), attaches to progesterone receptors and can be detected with a positron emission tomogrophy (PET) scan. When more progesterone receptors are present, the PET signal is higher.
The researchers recruited 43 postmenopausal women with oestrogen receptor-positive breast cancer. Most (86%) had metastatic disease, while 14% had locally advanced or locally recurrent disease.
The majority (72%) already had received some form of treatment before the start of the study.
Their prior treatment was most often a hormone therapy-based regimen.
The women underwent a PET scan using FFNP, followed by three doses of oestrogen over a 24-hour period, and then a second PET scan a day after the oestrogen treatment.
For 28 women, the PET signal in the tumour increased considerably after exposure to oestrogen, indicating that their oestrogen receptors were working and had responded to the hormone by triggering an increase in progesterone receptor numbers.
Fifteen women showed little to no change in progesterone receptor numbers after oestrogen treatment.
Then, the researchers followed the participants for six months or longer as they underwent hormone therapy as recommended by their individual oncologists. The disease of all 15 women whose tumours had not responded to oestrogen worsened within six months. Of the women whose tumours had responded, 13 remained stable and 15 improved.
“The goal of therapy is to control or improve disease, so if the therapy is likely to be ineffective, it should not be given to a patient,” said Dehdashti, who is also senior vice chair and division director of nuclear medicine at MIR. “We observed 100% agreement between the response to oestrogen challenge and the response to hormone therapy, even though the participants were on a variety of treatment regimens. This method should work for any therapy that depends on a functional oestrogen receptor, and it could provide valuable information to oncologists deciding how best to treat their patients.”
The researchers are now in the process of setting up a larger phase 2 clinical trial with collaborators at other institutions to verify their results.