Age Standardised Incidence and Mortality Rates
For breast cancer
Age Standardised
Incidence and Mortality Rates For breast cancer
In EU Countries
Age Standardised
Incidence and Mortality Rates For breast cancer
In Great Britain
Age Specific
Incidence Rates For breast cancer In Great
Britain
Modern Treatment
Has Resulted in 90%of White Women Surviving With
breast cancer
We know that there are certain risk factors for cancer although exactly how they work is not known.
Genetic and lifestyle factors have
important but incompletely understood roles.
Breast
Cancer and Family History
The significance of breast cancer in the family on the chance of another family member being affected is disputed. Early studies found the risk ratio (Q33.27) for developing
breast cancer to be 1.9 if the mother has had cancer of the breast and 2.3 if the disease had affected a sister. There is virtually no increased risk for more distant relatives. However, a meta-analysis (Q33.23) could find no evidence that there as an increased risk of
breast cancer even if a close relative had the disease. A meta-analysis of 51 studies, reported in The Lancet in 1997 evaluating the relationship between HRT and
breast cancer demonstrated no increased risk for those whose mothers or sisters have had
breast cancer to those with no family history.
For some women with a very strong history of breast or ovarian cancer it may be appropriate to test for the high penetrance
breast cancer susceptibility gene BRCA1 (breast cancer 1). This gene is located on chromosome 17. More intensive and frequent screening of those at increased genetic risk would appear to be appropriate. It is wise for the implications to be carefully addressed by a counsellor before the test is performed. It may be that we shall be able to provide a degree of reassurance, for some women at least, when there is a history of
breast cancer in the family.
Other genes are currently being evaluated in several research centres.
Hormones:
One cause of breast cancer is prolonged endogenous female sex
hormone production - early puberty and late
menopause.
This is supported by epidemiological evidence
and clinical trials confirming the therapeutic
benefit of anti-oestrogenic therapy in the
treatment and prevention of hormone- sensitive
(that is, oestrogen-receptor positive) disease.
However, breast cancer development is complex.
The association of HRT with an increased risk of breast cancer
is well recognized but has attracted disproportionate attention
following recent publications that have in turn resulted in conflicting advice from regulatory authorities. This
has reduced health professional and patient confidence in HRT
and triggered a dramatic decline in HRT prescribing.
In a few studies, reduced breast cancer mortality in women who
used hormone therapy before diagnosis have been observed . Due
to the high prevalence of past and current hormone use, it is
important to investigate whether these preparations are related
to breast cancer mortality.
To evaluate the influence of prediagnostic use of hormone therapy on breast cancer mortality,
a prospective cohort of 12,269 women ages 50 years or more
diagnosed with incident invasive breast cancer and residents of
Wisconsin, Massachusetts, or New Hampshire were enrolled in
three phases beginning in 1988. They were followed for death
until December 31, 2005, using the National Death Index. During
an average 10.3 years of follow-up, 1,690 deaths from breast
cancer were documented. Cumulative mortality from breast cancer
was lower among hormone therapy users, specifically current
users at the time of diagnosis, and oestrogen/progestogen users,
compared with nonusers. No association was observed for women
who were former or current users of oestrogen-alone
preparations. Although use of combined oestrogen/progestogen
preparations increases breast cancer risk, in this study, use of
these hormones before diagnosis was associated with reduced risk
of death after a breast cancer diagnosis.0801
breast cancer and Early pregnancy loss
Anti-Termination of Pregnancy Groups have claimed that pregnancy
termination increases the risk of breast cancer by 30%. There
would appear to be no foundation for this contention according
to a study by Michels et al.0701
They found no increased risk of breast cancer in women with a
history of pregnancy termination or spontaneous miscarriage.
breast cancer and the combined oral contraceptive pill.
Breast cancer is common with more than 600,000 new cases reported
internationally each year. Many studies have been undertaken to determine
whether the pill might place women at increased risk of breast cancer
The results of meta-analyses (Q33.23) are reasonably reassuring with at most a marginal increase. This must be balanced against several pill benefits including reduction in the risk of ovarian and endometrial cancer, fibroids, ovarian cysts, endometriosis, benign breast disease and ectopic pregnancy. Those women found to have
breast cancer whilst taking the pill are usually diagnosed at an early stage so that the prognosis is relatively good.
-
Every three minutes a woman in the
United States is diagnosed with breast
cancer. In 2006, an estimated 212,920 new
cases of invasive breast cancer were
diagnosed, along with 61,980 new cases of
non-invasive breast cancer. 40,970
women died in 2006 from this disease.
- breast cancer is the leading cancer
among white and African American women.
African American women are more likely to
die from this disease.
- breast cancer incidence in women has
increased from one in 20 in 1960 to one in
eight today.
Although the incidence of breast cancer has
been increasing, deaths have been falling -
Figure 1

Figure 1 Incidence
and mortality from breast cancer 1975 to 2005 in
Great Britain.
(http://info.cancerresearchuk.org/cancerstats/mortality/timetrends/)
Breast Cancer Screening Benefits - Mammograph
and Mammograms
Self-Examination:
- The majority of doctors would advocate self-checking on a regular basis.
More than 90% of breast cancers are found by the woman herself. If any
change is noted, early assessment by the doctor is to be highly recommended.
- The breast tissue becomes more nodular (lumpy) before each period so that it
is best to undertake examination after a period.
- The breasts are composed of
lobes of glandular tissue that can be felt between the thumb and the fingers
by gentle squeezing this is therefore not the method to examine the breast for lumps or thickening.
- The hand should be closed and flat with the fingers being gently but firmly pressed in and moved to feel for swellings.
- Imagine each breast in four quarters and systematically check each of these areas.
- Other changes such as discharge or bleeding from the nipple should also be reported to your general practitioner.
Mammography: Early breast cancer detection is the aim of screening by mammography.
The merits of a screening test are listed in
screening tests. With reference to
Q32.8:-
- Breast cancer is an important health risk (A). There are 24,000 new cases and 15,000 deaths reported annually in theUK .
- Breast cancer is the commonest cancer in women in theUK (B). One women in twelve (7.5%) will develop
breast cancer at some time in her life.
- The majority of breast cancers are found in women over the age of 55 years. We know a lot about the natural history of the disease (C). When the tumour is limited to a duct or measures less than 1 cm, spread to the lymph glands is least likely to have occurred. Screening aims to detect this early stage of disease.
- The five year survival for stage 1 breast
cancer (less than 2 cm) with appropriate treatment is 84% whereas it falls to 18% for stage 4 disease (D). The UK screening programme (mammography) costs 37 million per year.
- An evaluation in 1986 found that the cost per quality-adjusted life year (a year of good health quality) achieved by screening compared favourably to other approved and established screening programmes (E).
- Mammography has
- high specificity (low false negatives – (F)
- and sensitivity (low false positives - G).
In the three years from 1992, 4,729,003 women aged 50-65 were offered mammography –
3,582,332 (75.8%) accepted (H). Breast biopsies were required for 24,651 women (0.69% of those having mammograms.
breast cancer was identified 19,792 (0.55%). Cancer of 1 cm or less was found in 5,785 (0.16%).
It is not known if all invasive breast cancers begin as ductal carinoma in situ lesions
(pre-malignant). Not all early abnormalities
undergo calcification and mammography, looking
for calcification, may not be the most effective
way of diagnosing early lesions. A prospective
study from Germany has compared mammography with
MRI. The MRI proved more effective in diagnosing
early lesions.0701
Being screened for breast cancer reduced
breast cancer deaths by 48% in a study in East
Anglia following the introduction of screening
in 1989.2008
It might be assumed that computer assisted
detection of abnormality on mammography would
enhance interpretation. In practice, the use of
computer-aided detection is associated with
reduced accuracy of interpretation of screening
mammograms. The increased rate of biopsy with
the use of computer-aided detection is not
clearly associated with improved detection of
invasive breast cancer.0702
The ideal interval for breast cancer screening has yet to be established. The UK was one of the first to offer national breast screening with mammography. All women aged 50 – 64 are offered screening at three year intervals. The Department of Health is currently assessing the potential of extending the upper limit of screening to the age of 69. Most European programmes screen at two year intervals. A British trial looking at this interval is due to report in 1998. The Cancer Research Campaign is evaluating the possible benefits of mammography starting at age 40.
The breasts in younger women are usually too dense for interpretation of x-ray mammography. Sonography (ultrasound examination of the breast) is accurate but the investigation requires considerable expertise and is time-consuming.
Compression of the breast during mammography can be painful but the discomfort is just for a short time.
Mammography involves radiation. Current evidence suggests that, at most, mammography could be the cause of cancer in one woman for every two million women screened.
Whereas cervical screening is designed to pick up cervical disease before it becomes malignant,
breast cancer screening is designed to pick up the disease when it has already become active although hopefully early enough to provide curative treatment.
Nine out of ten women found to have an abnormality on mammography do not have cancer. If an abnormality is detected on the mammogram a sample of tissue is taken by the breast specialist often under local anaesthetic. A pathologist will then examine this biopsy microscopically to provide the definitive diagnosis. The emotive issues around breast screening, the need for quick evaluation and access to specialist consultation and treatment are being increasingly recognised by many units.
There is some concern that HRT (hormone
replacement therapy) reduces the
accuracy of mammography. Observational studies
have shown HRT to reduce sensitivity (ability to
detect an abnormality) and therefore increase
interval cancer rates (cancer diagnosed between
mammographic screens due to being missed at a
previous screen).9 HRT is also reported to
reduce specificity (ability to differentiate
cancer from non-cancerous change), leading to an
increase in false positive recall.0101
HRT is also reported to reduce specificity
(ability to differentiate cancer from
non-cancerous change), leading to an increase in
false positive recall.0601,
0602 However, only combined
therapy of oestrogen with progestogen,
significantly increases mammographic breast
density and hence potentially affects
sensitivity.9901
Almost all the increase occurs in the
first year and affects about 1 in 4 women. The
mammographic density increase with the combined
HRT is in the order of 6%.0501
Related Medical Abstracts - Click on the paper title:-
Breast Cancer Treatment
Premenopausal women with early breast cancer are usually
treated with tamoxifen and/or chemotherapy after
surgery. As their ovaries are producing oestrogen and
progesterone, it may be advantageous to suppress ovarian
function with Gonadotrophin Releasing Hormone (GnRH) if
the tumour is receptor positive. A meta-anlysis has
demonstrated their effectiveness. The optimum duration
of treatment is unknown.0701
Evidence from the International breast cancer Trialists Collaborative Group have found that any woman with hormone sensitive
breast cancer would benefit from tamoxifen regardless of her age or menopausal status. Tamoxifen has been shown to protect substantially against
breast cancer recurrence and death. These conclusions were derived from a meta-analysis
(Q33.23) of 55 trials involving 37,000 women. In the group of women with oestrogen sensitive tumours or those with unknown oestrogen sensitivity, there was a 47 % reduction in recurrence rate over ten years following five years of tamoxifen treatment. The survival rate was improved by 11 % over ten years. Tamoxifen was associated with a slight increase in the incidence of endometrial cancer.
For the past 30 years, tamoxifen has saved millions of lives throughout the
world. The same has been proven in randomized trials and meta-analyses.
Recent trials have shown clinical superiority of aromatase inhibitors over
tamoxifen in terms of disease free survival and reduction in complications.
However, because of the unique mechanism of tamoxifen, intrinsic advantages
and low cost, this wonder drug may still be a reasonable choice for hormonal
therapy in breast cancer.0801
Related Medical Abstracts - Click on the paper title:-
Support Groups
Members of a support group, provide each other with
various types of help and information for a particular
shared difficulty. The support may take the form of
providing relevant information, relating personal
experiences, listening to others' experiences, providing
sympathetic understanding and establishing social networks.
A support group may also provide ancillary support, such as
serving as a voice for the public or engaging in advocacy.
Support groups maintain interpersonal contact among their
members in a variety of ways. Support groups also maintain
contact through printed information rich newsletters,
telephone chains, internet forums, and mailing lists.
Support groups offer companionship and information for
people coping with diseases or disabilities. Support groups
may not be appropriate for everyone, and some find that a
support group actually adds to their stress rather than
relieving it.
Evaluation of the quality of Web sites is discussed
in(Q4.27) . You may find that several general women's health
sites may help you (internet information). The following are more specialised relevant Web sites:-
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Breast Cancer
Support Groups |
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http://www.breastcancercare.org.uk/
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| http://www.breastcancer.org/
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http://www.cancer.gov/cancertopics/types/breast |
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breast cancer Care |
Kiln House 210 New Kings Road
London SW6 4NQ32.33c (Tel 020 7384 2984) |
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Breast Care and Mastectomy Association (BCMA) |
26a Harrison Street, London WC1X 9JN (Tel: 020 7964 0260) |
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British Association of Cancer United Patients and Their Families and Friends (BACUP) |
121-3 Charterhouse Street, London, EC1M 6AA (Tel: 020 7608 1661) |
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CancerBACUP |
3 Bath Place Rivington Street London EC2A 3DR (Tel: 0207 696 9003) |
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Cancer Care Society
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James Scarth House 39 Hundred Romsey S15 HE Tel: 01794 830300 |
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CancerLink |
11-21 Northdown Street London N1 9NB (Tel: 0800 132905) |
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Cancer Relief MacMillan Fund
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Anchor House 15-19 Britten Street London
SW3 (Tel: 020 7351 7811) |
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Marie Curie Cancer Care |
28 Belgrave Square London SW1X 8QG
(Tel: 020 7235 3325) |
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Ovacome Ovarian Cancer Support Network |
C/O Shirley Lodge, 470 London Road Slough Berks SL3 8QY (Tel 01753 714333) |
DISCLAIMER
The aim of this web site is to provide a general guide and it is not intended as a substitute for a consultation with an appropriate specialist in respect of individual care and treatment.
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