According to the Mayo Clinic, hormone replacement therapy is a medication that contains female hormones. You take the medication to replace the estrogen that your body stops making during menopause. Hormone therapy is most often used to treat common menopausal symptoms, including hot flashes and vaginal discomfort.
Aromatase inhibitors can have a variety of side effects, including genitourinary problems associated with menopause such as vaginal dryness, itchiness, burning, overactive bladder, and urinary incontinence. Although these symptoms may be alleviated by the use of vaginal estrogen therapy (VET) or menopausal hormone therapy (MHT), there are concerns the therapies can increase the risk of breast cancer recurrence and death following treatment.
A large Danish observational cohort study concluded neither VET or MHT is linked with an increased risk of recurrence or mortality. However, a subgroup analysis discovered a higher risk of recurrence in women undergoing VET with adjuvant aromatase inhibitors, but not a higher risk of mortality.
The study included 8,461 postmenopausal Danish women between the ages of 35 to 95 years old who had been diagnosed with early-stage invasive ER-positive breast cancer between 1997 and 2004. Chemotherapy had not been given to the women. The individuals were randomly assigned to receive either 5 years of tamoxifen or an aromatase inhibitor, or both treatments in a sequence.
The researchers determined prescription data on hormone therapy, VET, or MHT from Denmark’s national prescription registry.
Among the 8,461 women who did not receive VET or MHT before their breast cancer diagnosis, 1,957 and 133 used VET and MHT after their diagnosis. The median follow-up for recurrence was 9.8 years, and for mortality, it was 15.2 years.
“In postmenopausal women treated for early-stage ER-positive breast cancer, neither VET nor MHT was associated with increased risk of recurrence or mortality. A subgroup analysis revealed an increased risk of recurrence, but not mortality, in patients receiving VET with adjuvant aromatase inhibitors,” concluded the authors of the study.
For more on HRT and breast cancer, head to the American Cancer Society.
The Breast Advocate® App is the World’s first breast cancer surgery shared decision-making app. Download it for free here.
According to new research, chemicals called parabens, which are common ingredients in everyday hair and personal care products, can encourage breast cancer cells in Black women.
In the United States, one in eight women will get breast cancer during their lifetime. Black women are more likely than any other racial or ethnic group to develop breast cancer before the age of 40.
“One reason for the higher risk of breast cancer may be exposure to harmful chemicals called endocrine-disrupting chemicals in hair and personal care products. These chemicals mimic the effects of hormones on the body.” shares lead researcher, Lindsey S. Treviño, Ph.D.
Parabens are common preservative ingredients used in cosmetic, personal hygiene, and food products to prevent the growth of bacteria and other microorganisms. The greatest exposure is believed to be through personal care products. Parabens enter the body via the skin or digestive system and have been detected in human tissues, blood, breast milk, placenta, and urine.
The study tested the effects of parabens on breast cancer cells from Black women. In both Black and white women, parabens increased expression of genes linked to hormone action in breast cancer cell lines. However, parabens only increased the growth of certain breast cancer cells in black women.
“These results provide new data that parabens also cause harmful effects in breast cancer cells from Black women,” Treviño said.
“While this project focuses on Black women, the knowledge we gain about the link between exposure to harmful chemicals in personal care products and breast cancer risk can be used to help all women at high risk of getting breast cancer,” concludes Treviño.
If you are facing surgery for breast cancer we want you to know you are not alone. Breast Advocate® provides evidence-based information and customized recommendations based on your diagnosis, personal preferences and values. It’s your treatment… our mission is to empower you to have the conversation you want to have with your doctors. Download the latest version of the Breast Advocate® app today.
According to a new study published in the online issue of Neurology®, women with multiple sclerosis (MS) are less likely to have breast cancers detected through routine cancer screenings than women without MS.
According to a new study published in the online issue of Neurology®, women with multiple sclerosis (MS) are less likely to have breast cancers detected through routine cancer screenings than women without MS.
Researchers looked at health care data for 14.8 million people in Ontario to see if there were any individuals diagnosed with breast or colorectal cancer who also had MS. For the study, they compared 351 women with breast cancer and MS to 1,404 women with breast cancer but no MS. They also identified 54 people with colorectal cancer and MS, and compared these to 216 people with colorectal cancer and no MS.
The team discovered that routine screening revealed breast cancer in 103 (29%) of the women with MS, and in 529 (38%) of the women without MS. After controlling for age, diagnosis year, and income, they found women with MS had a 32% decreased chance of having breast cancer diagnosed through routine screening.
“Disability from MS increases with age, as does cancer risk, so it is likely that those with MS may find it more difficult to get regular mammograms as they get older,” said study author Ruth Ann Marrie, MD.
Researchers also discovered that 21% of people with MS and breast cancer, and 33% of those with MS and colorectal cancer, had a level of impairment that required long-term care. “More research is needed regarding the role of MS-related disability on screenings,” states Marrie.
One limitation was the study did not include the time period from when a person first noticed cancer symptoms to when they told their doctor. “People experiencing marginalization due to race or ethnicity have different access to cancer screening, and this may be exacerbated among people with MS,” said Marrie. She stated that race and ethnicity data were not accessible for this study and that future research should look into it.
Regular screenings can help find cancers earlier before they have a chance to spread. Below are the American Cancer Society’s recommendations on breast cancer screening:
According to the CDC, some of the warning signs of breast cancer include:
If you notice any of these symptoms or something else that concerns you, schedule an appointment with your doctor right away.
If you are facing surgery for breast cancer, or are considering surgery to decrease your risk of developing breast cancer – Breast Advocate® is for you.
According to a recent study, a lumpectomy is as effective as a mastectomy in women with non-metastatic breast cancer under the age of 40. Young women with early stage breast cancer who have breast-conserving surgery (lumpectomy and radiation) have the same survival rate as women who have a mastectomy. These findings show that advising patients on outcomes is critical in decreasing the unnecessary morbidity from surgical procedures that may not be indicated, given the increased use of mastectomy within this age group.
“[The study] results also emphasize the need for future attention on racial outcome disparities in young women,” Christine Pestana, MD, – said during the presentation, a researcher at the Oncology Department of Breast Surgery at the Levin Cancer Institute Atrium Health.
According to Dr. Pestana, 1 in 68 women will develop breast cancer by the age of 40, and these women are more likely to have advanced-stage disease at the time of diagnosis compared to older women.
“Outcome disparities persist between the two groups,” Dr. Pestana goes on to say that “mastectomy rates are increasing in younger patients despite lack of data supporting improved survival [compared to lumpectomy and radiation].”
The researchers evaluated the relationship between survival and surgical approach among approximately 591 women under the age of 40 (66% white, 25.9% black). These women are part of the Lewin Cancer Institute’s database of young women who have had surgery for nonmetastatic breast cancer. About a third (35.5%) of these women had a lumpectomy and the remaining (64.5%) had a mastectomy.
Researchers compared patient age, race, BMI, disease stage, grade, molecular subtype, lymphovascular invasion, extranodal extension, type of surgery, use and timing of chemotherapy, and hormone therapy use.
After a median follow-up of 5.5 years, 72% of women (12%) were deceased. More than half of the women (53.3%) had hormone receptor-positive, HER2-negative cancer, 20.8% had hormone receptor-positive/HER2-positive cancer, 19.3% had triple-negative cancer, and 6.6% had HR-negative/HER2-positive cancer.
There was no difference in overall survival between women who underwent mastectomy and those who had breast-conserving surgery. Most (85.4%) women with HR-positive/HER2-negative disease received antiestrogen therapy. Researchers observed a 2.9-fold increased risk for death among women who had not been treated with hormone therapy compared to those who had hormone therapy.
Black patients had a higher risk of death in all molecular subtype groups. Even after researchers accounted for all other risk factors, multivariate analysis showed black women with triple-negative breast cancer had a 5.7-fold higher risk of dying.
“The results are particularly significant because younger women are increasingly being diagnosed with breast cancer, despite low rates overall, and a growing number are undergoing mastectomy and even prophylactic bilateral mastectomy rather than breast-conserving surgery,” Pestana said.
Clinical trials have also shown that women choosing to have lumpectomy and radiation have an overall rate of local recurrence at 5 years of less than 5%. This statistic compares similarly with mastectomy local recurrence rates.
While several studies show lumpectomy and radiation is associated with (at least) the same overall survival as removing the entire breast, there is no “one size fits all” approach to breast cancer surgery. There are many factors that patients will need to consider in deciding the best approach for their individual situation. Ultimately, the final decision should be reached using a shared decision-making approach between the patient and their healthcare team.
The Breast Advocate® App is the World’s first breast cancer surgery shared decision-making app. Download it free here.
New research performed in Sweden has found a key protein that protects against breast cancer tumor growth. The recent discovery at the Karolinska Institute in Sweden also showed that estrogen receptor (ER) negative breast cancer patients with higher levels of this protein, known as GIT1, have a better prognosis.
Breast cancer affects 1 in 8 American women at some point in their lives. Unfortunately, there are fewer treatment options for ER-negative breast cancers, which lack estrogen receptors (ER) and do not respond to anti-estrogen hormone therapy. Triple-negative breast cancers, which lack estrogen, progesterone, and HER2 receptors, are very difficult to treat since they lack the receptors that mainstay breast cancer treatments target.
“Identification of new molecular mechanisms that regulate the growth of ER-negative breast cancer is warranted, as these mechanisms may represent novel therapeutic targets,” explains Per Uhlén, professor at the Department of Medical Biochemistry, Karolinska Institutet.
Professor Uhlén and his team at the Department of Medical Biochemistry, Karolinska Institutet discovered a novel way by which the GIT1 protein regulates ap rocess known as Notch signaling. Overactive Notch signaling affects the development and progression of ER-negative breast cancer and has previously been linked to a worse prognosis.
“Our results provide important information about a mechanism that controls the initiation and growth of breast tumours,” continues Professor Uhlén. These study results could potentially lead to the development of new treatments for hard-to-treat types of breast cancer that do not respond to first-line therapies.
Professor Uhlén’s research group is working closely with physicians who treat cancer patients to focus on research areas that are critical to patient care.
“We want to conduct research that can benefit patients with severe diseases,” says Professor Uhlén. “At Karolinska Institutet, we have state-of-the-art tools and equipment that can push the development of new therapies.”
Screening mammograms save lives. However, studies also show they can lead to overdiagnosis of breast cancer. Overdiagnosis occurs when the tumors that are found would never have caused harm if they had not been detected. New research has found that this happens less often than experts previously thought.
Among women who have routine mammogram screening every 2 years between the ages of 50 and 74, about 1 in 7 breast cancers detected will be overdiagnosed. This is lower than previous reports that quoted estimates as high as 30%.
Dr. Katrina Armstrong of Massachusetts General Hospital in Boston states, “The good news is, it’s less common than we thought.”
According to Armstrong, the issue with overdiagnosed cancers is that they lead to unnecessary treatment and emotional baggage. Still, the chances of that happening are low for anyone undergoing breast cancer screening.
Approximately 7 in 1,000 women are diagnosed with breast cancer through mammography screening. According to the latest estimate, about 1 in 1,000 women who undergo screening will be diagnosed with a cancer that would not have caused any harm in the first place.
“Assuming that 60% of the 280,000 cases of breast cancer diagnosed in the United States each year are found through mammography screening, eliminating overdiagnosis could spare 25,000 women the cost and complications of unnecessary treatment,” shares Armstrong.
“No screening test is perfect, and there are always downsides,” said senior study author Ruth Etzioni.
Finding a tumor that would never have developed to the point of causing harm might lead to overdiagnosis. In other circumstances, the tumor is developing but would not have progressed to a “clinical disease” before the individual died of another cause.
According to Armstrong, the field has a “duty” to prevent overdiagnosis, and overtreatment, as much as possible. She believes it is possible, based on ongoing research. Studies are underway to increase the accuracy of screening technologies and to find better strategies to predict the progression of breast cancers.
More information on breast cancer early detection can be found at the American Cancer Society.
According to Dr. Svasti Haricharan, lead author of a recent study, “Society has internalized the narrative that lifestyle factors are to blame for racial differences in [breast cancer] outcomes, so most scientists don’t look at molecule-level differences between people.”
Researchers compared estrogen receptor-positive (ER-positive) cancerous tissue from black and white women with normal breast tissue. They discovered that eight DNA damage response and repair (DDR) genes in black women functioned differently in black women.
The repair response was inhibited by some of the dysregulated DDR genes.
Dr. Haricharan continues, “What we’re seeing here is a tangible molecular difference in how these cells repair damaged DNA – a critical factor in the development of cancer – which affects how cells grow and reproduce in tumors.”
This study proves that how patients do after a breast cancer diagnosis is certainly not just dependent on lifestyle factors. More importantly, doctors may need to adjust treatment plans for black women with breast cancer based on the findings of the study.
“This is something we can act upon immediately because helping these women is less about finding a new drug and more about changing the timing for treatments we already have available,” explains Dr. Haricharan.
Doctors use cyclin-dependent kinase inhibitors in the later stages of treatment for ER-positive breast cancer. They may be able to introduce this earlier in the treatment of black women with breast cancer, giving them a better prognosis.
Dr. Haricharan spoke with Medical News Today about the research and the team’s future plans.
“Black women are severely underrepresented in virtually all datasets of patient tumors, so a lot of previous results about breast cancer only accurately reflect what’s happening to white women,” said Dr. Haricharan. “We hope our research will highlight the need to study cancer in different racial and ethnic groups more closely and improve outcomes for historically marginalized patients.”
According to a recent study led by researchers at the National Cancer Institute’s (NCI) Center for Cancer Research, an experimental form of immunotherapy that uses an individual’s own tumor-fighting immune cells could potentially be used to treat people with metastatic breast cancer. The study found that most women with metastatic breast cancer can build an immune response against their tumors, which is required for this type of immunotherapy and relies on TILs (Tumour-Infiltrating Lymphocytes).
In a clinical trial of 42 women with metastatic breast cancer, 67% established an immune response against their cancer. Six women were treated with this method, with half of them experiencing a significant tumor decrease in tumor size.
Mutations in tumor DBU create abnormal cells called neoantigens. TILs can target neoantigens that the immune cells cannot recognize. When mutations in tumor DNA occur, neoantigens are created. Other types of immunotherapy have been proven to be beneficial in treating cancers, such as melanoma, that have many mutations and neoantigens. Its effectiveness in cancers that have fewer neoantigens, such as breast cancer, however, has been less clear.
The goal of this study was to see if using immunotherapy to treat metastatic epithelial-type cancers, such as breast cancer, could result in tumor regression.
In the trial, researchers used whole-genome sequencing to find mutations in tumor samples from 42 women with metastatic breast cancer whose cancers had progressed despite conventional treatments. TILs were extracted from the tumor samples, and their reactivity against neoantigens produced by the various tumor mutations in the tumor was examined in lab testing. TILs recognized at least one neoantigen in twenty-eight women. Almost all of the neoantigens discovered were specific to each patient.
The researchers developed the reactive TILs to large numbers in the lab for each of the six women who were treated. Next, they gave each patient intravenous infusions of the immune cells. All of the patients received four doses of pembrolizumab (Keytruda), a checkpoint inhibitor, before the infusion to prevent the newly introduced T cells from becoming inactivated.
The study reported that “objective tumor regression was noted in three patients, including one complete response (now ongoing over 5.5 years) and two partial responses (6 and 10 months).
The researchers recognized that the use of pembrolizumab could raise questions about its impact on the outcome of the TIL therapy. However, they determined that treatment with such checkpoint inhibitors alone has not previously resulted in long-term shrinkage in people with hormone receptor-positive metastatic breast cancer.
This study shows that most patients with breast cancer are able to generate a natural immune response to their tumors. Most patients with breast cancer generated a natural immune response which could potentially be harnessed to improve breast cancer treatment with immunotherapy in the future, particularly for those who don’t respond to standard therapies.
According to research published in the JAMA Network Open, the combination of having dense breast tissue and a high body mass index (BMI) increases the risk of developing breast cancer, with a stronger association identified among postmenopausal women.
Both factors should be included in risk classification in population-based screening, explained Thi Xuan Mai Tran, Ph.D., from Hanyang University in South Korea.
“Women with obesity and dense breast tissue might benefit from tailored early screening strategies to detect breast cancer,” states Tran.
Dense breast tissue and obesity are both known to be significant risk factors for breast cancer. However, how these two factors combine is not clear, particularly when it comes to menopausal status.
Tran’s team sought to look at the relationship between breast density, BMI, and menopausal status. The team looked at data from the Korean National Cancer Screening Program, which included 3.2 million premenopausal women with an average age of 45 years and 4.4 million postmenopausal women with an average age of 60 years. Premenopausal women were found to have 34,466 cases of breast cancer, while postmenopausal women had 30,816 cases.
The researchers found that increased breast density was linked to a higher risk of breast cancer in both premenopausal women across all BMI groups.
Without taking BMI into account, premenopausal women in the BI-RADS 4 category had twice the risk of breast cancer compared to those in the BI-RADS 1 category who were underweight.
When breast density and BMI were paired with breast cancer risk, Tran’s team discovered that high breast density and high BMI had a “significant” positive interaction for both premenopausal and postmenopausal women, with the latter having the strongest effect.
“Our findings suggest that breast density notification should be provided not as a stand-alone risk factor but as an adjunct factor with BMI for risk stratification in population-based mammographic screening settings for public health significance,” the researchers concluded.
Be sure to discuss your breast density and weight management with your healthcare team. It is very important to know if you have dense breasts as you may benefit from a tailored breast cancer screening strategy to increase the chances of early detection.
According to a recent study, at least 1 in every 10 patients diagnosed with breast cancer require treatment for depression. Unfortunately, patients generally don’t get the care they need unless doctors screen them for the mental health disorder. About 1% of breast cancer patients who were not screened were ultimately diagnosed with depression, data showed.
The findings are based on an analysis of a program introduced by the Kaiser Permanente health system in 2017 to identify cancer patients who need behavioral healthcare. This program successfully guided 7% of breast cancer patients with depression into the treatment they needed.
“Early identification and treatment for mental health issues is critical, yet depression and other mental health issues are often under-identified and under-treated in breast cancer patients,” study co-author Erin E. Hahn said.
“Our study showed that the use of implementation strategies to facilitate depression screening is highly effective … [at helping] our cancer patients achieve the best possible health,” states Hahn, a research scientist with Kaiser Permanente Southern California in Los Angeles.
According to the National Institute of Mental Health, over 20 million people in the United States are diagnosed with depression each year.
Research suggests that roughly 25% of patients diagnosed with breast cancer develop this mental illness, which produces chronic feelings of sadness, loss of interest in daily activities, loss of energy, difficulty sleeping, and even thoughts of suicide. Some types of breast cancer treatment, such as chemotherapy, hormone therapy, and surgical removal of the ovaries can increase the risk of depression.
Hahn and her colleagues enrolled 1,436 breast cancer patients treated by Kaiser Permanente doctors for this study. Patients were divided into 2 equal-sized groups and either received specific screening for depression followed by tailored interventions, or education only.
Among those who completed the screening, 10% had scores that indicated a need for mental health care. Furthermore, patients who were screened were more likely to be referred to behavioral care and required fewer oncology visits.
“The trial of this program was so successful that we have rolled out depression screening initiatives across all our Kaiser Permanente medical oncology departments in Southern California,” study co-author Hahn said.
“We are incorporating the lessons learned from the trial, particularly the importance of ongoing audit and feedback of performance and are encouraging our clinical teams to adapt the workflow to meet their needs,” she said.
Depression is a mental illness and is a lot more than just not feeling yourself for a few days. If you can’t shake the feeling of sadness, are disinterested in life activities, or are having problems coping in any way, please reach out to your healthcare team for help.