Active Smoking
Linked To Increased Risk Of Breast Cancer
Non-Smokers Exposed
To Smoke Were Not At A Higher Risk
Active smoking appears
to play a larger role in the development of breast cancer than
previously thought, according to a study reported in the Journal
of the National Cancer Institute.
Tobacco smoke contains
a number of human carcinogens, and metabolites of cigarette
smoke have been found in the breast fluid of smokers.
However, studies examining
the association between tobacco smoke and breast cancer risk
have yielded inconsistent results, experts say.
The authors of the
new study say that many studies have not been able to independently
assess the contributions of the timing of exposure, age of diagnosis,
or genetic susceptibilities to the overall risk of breast cancer.
In addition, many
of these studies did not consider passive smoking exposures,
or exposure to secondhand smoke, among nonsmokers.
Dr. Peggy Reynolds
of the California Department of Health Services and her colleagues
examined breast cancer risk among 116,544 women in the California
Teachers Study who had reported their smoking status on a survey
given to them when they enrolled in the study.
Between 1996 and 2000,
2,005 of the women were diagnosed with invasive breast cancer.
The incidence of breast
cancer among current smokers was approximately 30% greater than
that among women who had never smoked, irrespective of whether
they were compared to women who had or had not been exposed
to passive smoking, the authors report.
Analysis of subgroups
of active smokers revealed increased breast cancer risks among
women who started smoking before age 20; who began smoking at
least five years before their first full-term pregnancy;
and who had a longer duration of smoking or who smoked 20 or
more cigarettes per day.
Current smoking was
associated with increased breast cancer risk in women without
a family history of breast cancer but not among women with a
family history of the disease.
There was no statistically
significant increase in breast cancer risk among former smokers,
and there was no evidence of a link between passive smoking
exposure and breast cancer risk.
Always consult your
physician for more information.
Risk
Factors for Breast Cancer
Any woman may develop
breast cancer. However, the following risk factors may increase
the likelihood of developing the disease.
Risk factors that
cannot be changed:
-
gender
Breast cancer occurs nearly 100 times more often in women
than in men.
-
aging
A majority of cases occur after age 50.
-
personal history of breast
cancer
-
previous breast irradiation
-
family history and genetic
factors
Having a close relative, such as a mother or sister, with
breast cancer increases the risk. This includes changes
in certain genes such as BRCA1, BRCA2, and others.
-
-
previous breast biopsy in
which the tissue showed atypical hyperplasia
-
menstrual periods that began
early in life
-
menopause began later in
life
The most frequently
cited lifestyle-related risk factors:
-
-
not having children, or first
child after age 35
-
-
obesity and a high-fat diet
-
-
-
long-term, post-menopausal
use of combined estrogen and progestin (HRT)
-
weight gain and obesity after
menopause
Environmental risk
factors:
-
Exposure to pesticides, or
other chemicals, is currently being examined as a possible
risk factor.
Always consult your
physician for more information.
Online
Resources
(Our Organization
is not responsible for the content of Internet sites.)
American
Cancer Society
American
Society for Clinical Oncology
Centers
for Disease Control and Prevention (CDC)
National
Institutes of Health (NIH)
National
Women's Health Information Center
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February 2004
Risk
Factors for Breast Cancer
Tailoring
Adjuvant Therapy for Early-stage Breast Cancer Studied
Online
Resources
Tailoring
Adjuvant Therapy for Early-stage Breast Cancer Studied
Although chemotherapy
and ovarian function suppression are both effective adjuvant
therapies for patients with early-stage breast cancer, little
is known of the efficacy of their sequential combination (how
well the treatment works when given in a certain order), state
researchers in a new study report.
Adjuvant therapy is
a term used to describe when physicians choose more than one
therapy in treating a patient, specifically the therapy is given
after the primary cancer treatment is completed in order to
improve the chance of a cure.
A new study by the
International Breast Cancer Study Group (IBCSG)
concludes that premenopausal women with lymph node-negative
breast cancer should receive adjuvant therapy tailored according
to the estrogen receptor status of the primary tumor.
The study was reported
in the Journal of the National Cancer Institute (JNCI).
Patients with estrogen
receptor (ER)-negative, or endocrine nonresponsive, breast
cancer should receive adjuvant chemotherapy, according to the
study, whereas for patients with ER-positive, or endocrine responsive,
tumors, the use of endocrine therapy alone or in combination
with adjuvant chemotherapy requires further study.
Some studies have
suggested that cytotoxic chemotherapy benefits premenopausal
women with breast cancer because it causes premature menopause.
The new study addresses
whether adjuvant ovarian function suppression can be used as
a replacement for or as a supplement to cytotoxic adjuvant chemotherapy
for premenopausal women with early-stage breast cancer.
In an editorial commenting
of this study in the JNCI, the authors said,
"These findings support the idea that ovarian suppression "is
a viable treatment alternative for at least some premenopausal
women with breast cancer." The authors, Dr. Joseph L. Pater
and Dr. Wendy R. Parulekar, are physicians at the National
Cancer Institute of Canada Clinical Trials Group at
Queen's University in Kingston, Ontario.
In the study, Dr.
Monica Castiglione-Gertsch, a member of the IBCSG,
compared outcomes of 1,063 pre- and perimenopausal women who
were previously treated for lymph-node negative (early-stage)
breast cancer and randomly assigned to receive adjuvant chemotherapy,
adjuvant therapy with the ovarian function suppression drug
goserelin, or adjuvant chemotherapy followed by goserelin.
The women were tested
to determine the estrogen receptor status of their tumors.
After a median follow-up
of seven years, there was no difference in disease-free
survival or overall survival among patients in the three treatment
groups.
However, a subgroup
analysis showed that patients with ER-negative tumors who
received chemotherapy alone or followed by goserelin had better
disease-free survival than patients who received goserelin alone.
By contrast, among
patients with ER-positive tumors, results were similar after
chemotherapy alone or goserelin alone. Sequential use of chemotherapy
followed by goserelin resulted in a statistically nonsignificant
benefit that was limited to younger women.
The study authors
caution that the study findings "should not alter current
patient care, but rather emphasize the relevance of current
studies of chemotherapy and endocrine agents."
Drs. Pater and Parulekar
agree, recommending that future studies examine the selective
use of ovarian suppression in women who are not rendered menopausal
by chemotherapy.
Always consult your
physician for more information.
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