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Biomarkers Needed for Premenopausal Women With Breast Cancer

Danielle Bucco
Published: Sunday, Sep 17, 2017

Dr. Ruth O'Regan
Ruth O'Regan, MD
Molecular profiling could help differentiate which premenopausal women with ER-positive breast cancer need extended adjuvant therapy and which need ovarian function suppression, with ongoing studies hoping to find a biomarker to help guide treatment selection, according to Ruth O’Regan, MD, at the 2017 Lynn Sage Breast Cancer Symposium.

A host of clinical trials have added new questions into the treatment landscape for patients with ER-positive breast cancer, such as the ATLAS trial, which demonstrated benefits for continuing adjuvant therapy with tamoxifen for 10 years compared with 5 years. Moreover, the TAILORx trial has indicated that chemotherapy may not be needed for all patients and findings from the Suppression of Ovarian Function (SOFT) and Tamoxifen and Exemestane Trial (TEXT) trials showed potential benefits for ovarian suppression in select patients, although not all experienced outcomes that outweighed the potential risks.

“Breast cancer in premenopausal women is biologically different but only because they get more TNBC and less Luminal A cancers. I think that there are premenopausal patients who are going to do just fine, since they have low-risk cancers,” said O’Regan, a professor of Medicine that University of Wisconsin School of Medicine and Carbone Cancer Center. “The assays that we use right now are applicable to these women. We need to hone in on getting a biomarker that tells us who needs ovarian suppression because that is a big issue for these women, since it is hard to take. For women under 35, the lack of adherence was 20%, which is quite high.”

In an interview with OncLive, O’Regan, discussed potential biomarkers, such as Ki-67, that could help tailor treatment for patients, specifically younger, premenopausal women. Moreover, she discussed the potential for the 21-gene recurrence score Oncotype DX, the 70-gene signature MammaPrint, and the Breast Cancer Index, which looks at 7 genes.

OncLive: Can you describe some of the ongoing biomarker research that is ongoing?

O’Regan: We use molecular assays to make a lot of decisions in ER-positive breast cancer. It would be interesting to use one of the existing assays such as 21-gene recurrence score, 70-gene signature, or the Breast Cancer Index, to determine which patients really need this more intensive endocrine therapy approach. The good news is that they have samples in about 80% of the patients that entered SOFT and TEXT. At this point, no RNA has been extracted but I think that is something that we will see. It's just a question of will one of these trials pan out as something that will make sense as a biomarker for these patients. 

How do premenopausal patients differ from other groups?

Overall, only about 20% of breast cancers we see occur in women that are still having regular periods. Less than 10% occur in women of the age of 40 and less then 2% in women under the age of 35. If one looks biologically, what is found is that they are more likely to get triple-negative breast cancer (TNBC) and less likely to get Luminal A cancer. There is data demonstrating that as the age increases the rate of TNBC goes down whereas the rate of Luminal A goes up. 

However, if you look at the molecular profiling assays that we use to make decisions, such as the 21-gene recurrence score or the 70-gene signature, there was about a third of premenopausal patients under the age of 50. Some of those patients had low-recurrent score cancers and there was no reason to believe that they didn't do fine without chemotherapy. Even though they biologically get more aggressive cancers, I still think the assays that we use are applicable to these younger women.

How is adjuvant therapy different for these patients?

When you look at adjuvant therapy, we treat pre- and postmenopausal women the same when it comes to chemotherapy, whether they have TNBC, HER2-positive cancers, or even estrogen receptor (ER)-positive cancers. The big difference is how we manage them from an endocrine therapy perspective. For decades, using tamoxifen for 5 years was the standard, but more recently we’ve used it for 10 years. The SOFT and TEXT trials looked at either adding an ovarian suppression with either tamoxifen or an aromatase inhibitor in women who were undergoing ovarian suppression. This showed a modest difference in favor of adding ovarian suppression. 

One of the key things we don't know is which patients need this approach and it is more toxic. We don't know the long-term toxicities of these approaches. One of the things that we used to make decisions are women of younger age, because there was a benefit for women under the age of 35. We reviewed some data showing that if you have cancers that have low progesterone receptor and high Ki-67 and have received chemotherapy, they appear to benefit from either the addition of ovarian suppression or an aromatase inhibitor.

Going forward, finding the molecular profiling biomarker to tell us which patients need this approach is going to be important. The other problem with SOFT and TEXT is that they compared it to 5 years of tamoxifen and we now very often give 10 years of tamoxifen or 5 years of an aromatase inhibitor after tamoxifen. 

What are the specific challenges that premenopausal patients face?
One of the big challenges for premenopausal patients is typically the younger patients trying to maintain fertility. We have fairly good data suggesting that if you give ovarian suppression during the duration of chemotherapy, they are not as likely to develop permanent ovarian failure and are more likely to get pregnant.

One trial that recruited patients with ER-positive breast cancer showed an improved disease-free survival if you gave ovarian suppression through chemotherapy. That is one of the things that they struggle with. A lot of times, I'll see patients who are told that they can never get pregnant, which is not true. I have had a lot of patients that got pregnant after a diagnosis of breast cancer. We usually want them to wait at least 2 years, if not longer. If they are taking tamoxifen, they can stop it and then restart it later.

The other issue to keep in mind is that these women are undergoing these therapies when they're quite young so we are not sure what is going to happen to their bones or in terms of coronary heart disease. The SOFT and TEXT studies did show that there was an increased rate in hypertension and glucose intolerance in patients who got ovarian suppression, which is slightly worrying. We don’t know the long-term side effects of this ovarian suppression on these women and that is important to investigate. 

For young women, a very good organization is the Young Survival Coalition because if you have questions they will be a very useful group to touch base with.



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