The study reviewed here suggests that several hormone-related health factors may affect the risk of developing specific types of breast cancer.
The researchers compared the health histories of more than 1,000 women aged 55 to 79 who were diagnosed with breast cancer to the health histories of about 1,500 similar women who weren't diagnosed with breast cancer. The diagnosed breast cancers were of three different types:
The study found that:
Hormone-receptor-positive breast cancer is more common and has a better prognosis than HER2-positive and triple-negative breast cancers. Hormones play an important role in the development and growth of hormone-receptor-positive breast cancers. Hormonal therapy medicines can effectively treat this type of breast cancer and can lower the risk of the breast cancer coming back.
The targeted therapies Herceptin (chemical name: trastuzumab) and Tykerb (chemical name: lapatinib) are used to treat HER2-positive breast cancers. Herceptin also can be used to lower the risk of HER2-positive breast cancer coming back.
Triple-negative breast cancer can be challenging to treat since hormonal therapies and targeted therapies aren't as effective in treating this type of breast cancer. Chemotherapy and radiation therapy can be used to treat triple-negative breast cancer.
Deciding to breast feed or to use HRT are personal choices that you can control. You can't control when you start having periods or when you start to go through menopause. A better understanding of any links between health factors -- whether or not they can be controlled -- and the development of different types of breast cancer can offer doctors more clues about how different types of breast cancer happen as well as how to treat each type.
This study found that the risk of hormone-receptor-positive breast cancer was 70% higher in women who used combination HRT compared to women who didn't use HRT. Other research has shown a similar link between HRT use and higher breast cancer risk. Still, the side effects of menopause, such as hot flashes, can dramatically reduce quality of life for some women. These women have to weigh the benefits of HRT against the risks.
If you're having severe hot flashes or other menopausal side effects and are considering taking HRT, talk to your doctor about:
Together, you and your doctor can decide if HRT or another treatment to ease menopausal side effects might be right for you. If you decide to use HRT, try to make healthy lifestyle choices (eating a healthy diet, exercising) that can lower your breast cancer risk. During and after HRT, make sure to follow recommended breast cancer screening guidelines, including monthly breast self-exams, annual mammograms, and annual physical exams by your doctor.
SEATTLE, Aug. 25 (MedPage Today) -- Different molecular subtypes of breast cancer appear to be influenced by specific reproductive factors, investigators here reported.
Early age at menarche almost tripled the odds for HER-2 overexpression, whereas late age at menopause and use of combined hormonal therapy significantly increased the risk of luminal disease, reported Amanda I. Phipps, of the Fred Hutchinson Cancer Research Center here, and colleagues, in the Oct. 1 issue of Cancer.
Breastfeeding for at least six months had a protective effect against luminal and triple-negative (estrogen and progesterone receptor, HER-2) disease, the researchers found.
"Our data do support the premise that risk factor profiles vary by breast cancer subtype and that hormonal risk factors have a greater impact on luminal-type breast cancers than HER 2-overexpressing or triple-negative tumors," they said.
"Further research is needed to clarify the epidemiology of [HER-2 overexpressing and triple-negative] tumors because at the current time no consistent risk factors for either of these 2 subtypes have been identified," the researchers concluded.
Gene expression studies have identified five breast cancer subtypes: luminal A and B, HER 2-overexpressing, basal-like, and unclassified.
Luminal tumors are characterized by expression of the estrogen receptor, which is usually accompanied by expression of the progesterone receptor. The protein kinase HER-2/neu is upregulated in HER 2 overexpressing tumors. Basal-like and unclassified tumors constitute the triple-negative phenotype.
"Compared with luminal tumors, both HER 2-overexpressing and triple-negative tumors have a poorer prognosis," the authors said. "However, to our knowledge, differences in the epidemiology of these subtypes are not well defined."
Examination of risk factors by tumor subtype may reveal disease-specific associations that go unrecognized when the subtypes are grouped together, they theorized.
So in the current study, the investigators examined reproductive influences on tumor subtype in patients from two population-based, case-control studies of breast cancer.
The two studies involved women ages 55 to 79 and included 1,023 cases of luminal breast cancer, 39 cases of HER 2-overexpressing breast cancer, 78 cases of triple-negative disease, and 1,476 controls.
Using logistic regression to compare each case group with controls, the authors found that early age at menarche increased the odds ratio for HER 2-positive breast cancer by 2.7 (95% CI, 1.4 to 5.5).
Early menarche did not significantly affect development of the other disease subtypes.
Breastfeeding for at least six months reduced the risk of luminal breast cancer (OR 0.8, 95% CI 0.6 to 1.0) and triple-negative disease (OR 0.5, 95% CI 0.3 to 0.9).
The risk of luminal disease was increased by 60% in women who were older at menopause (OR 1.6, 95% CI 1.1 to 2.2) and by 70% in women who used combined estrogen-progestin hormone therapy (OR 1.7, 95% CI 1.3 to 2.1).
Neither parity nor age at first live birth influenced the development of any of the molecular subtypes.
The researchers acknowledged that the statistical power of their analysis was limited by the inclusion of only 78 triple-negative and 39 HER-2-overexpressing cases.
Nor was it possible, they said, to distinguish between basal-like and unclassified cases and other misclassification of case subtypes was possible.
The study was supported by the National Cancer Institute and the National Center for Research Resources.
The authors reported no conflicts of interest.
Primary source: Cancer Source reference: Phipps AI et al. "Reproductive and hormonal risk factors for postmenopausal luminal, HER-2-overexpressing, and triple-negative breast cancer" Cancer 2008; DOI: 10.1002/cncr.23786.
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