Screening for breast cancer

Changed by Candace Makeda Moore, 31 Oct 2019

Updates to Article Attributes

Body was changed:

Screening for breast cancer includes activities which test members of asymptomatic populations for breast cancer. Many advanced countries have breast screening programs. The most widely adopted method for breast cancer screening is mammography.

There are few areas in imaging specifically and medicine in general, fraught with more controversy than screening for breast cancer. Due to the emotive issues surrounding the diagnosis, the scientific literature on breast screening and its issues reaches the lay press quickly and is sometimes reproduced in non-scientific, often potentially inaccurate terms. 

Mammography is notAny screening examination, like any test in medicine, will have a perfect studyfalse negative and ita false positive rate. Mammography as a screening exam does not find all cancers in all women, and will in some cases be read as positive in women without cancer. But until a cure is found, thisNonetheless mammography is currently believed to the best universally available tool we have to find breast cancers reliably and reproducibly early in the disease process.

The rationale behind screening

The rationale behind screening for breast cancer is the universally accepted dictum that (all other factors being equal) earlier diagnosis results in increased survival. The smaller the cancer at the time of diagnosis, the better the 5 year survival of breast cancer.

In general, if a breast cancer is found at less than a 1 cm diameter, the 5 year survival is the same as the general population at large. Screening for breast cancer is often cost and risk effective, feasible and evidence-based.

Historical background 

The increased survival, however cost, risks and treatments available vary dramatically in breast cancer is due in part to earlier diagnosis but also markedly improved treatments. 

The previously used radical surgical therapies for breast cancer are now a thing ofdifferent populations around the past. Lymphoedema used to be a very significant, dreaded complication of mastectomy and is now a rare occurrence in clinical practiceglobe.

Not only are more women surviving this disease, they are doing it with cosmetically acceptable results. This is a direct result of the use of screening mammography. Treated patients may now enjoy a good quality of life without the radical surgical interventions previously used which were often associated with unpleasant sequelae.

The initial literature support came from the Two Counties Trial in Sweden. Follow up for the trial participants continues and the data support the continued use of screening to detect breast cancer at an early stage when the therapy is potentially curative and cosmetically acceptable. The Two Counties trail and the subsequent Health Insurance Plan (HIP) study in New York showed a decrease in deaths from breast cancer in those aged 40-74 years. A direct result of the HIP study was that screening was introduced in the USA.

Since screening was introduced in the US, the mortality rate from breast cancer has declined by 30%; it had stayed constant from the Second World War.

The concept of risk

As it pertains to screening and breast cancer, there is significant confusion among the general population and many professionals about the concept of risk.

Approximately 10% of breast cancers have a first degree family history of breast cancer. This means that 90% or more of the cases will be sporadic, i.e. due to spontaneous mutations in patients with no known family history.

A common occurrence seen regularly is the reaction when someone is told they have a breast malignancy and invariably the reaction is "but I don't have a family history" or "no one in my family has breast cancer". This unfortunate state of affairs is further compounded by the potentially misleading term "average risk" when used in the context of breast cancer. This is a misnomer. Women with a positive family history are at exceptional risk; women with no family history are at risk because of their gender. The unthinking use of "average risk" inadvertently implies that we should concentrate our efforts at the 10% or that the 90% with no history can somehow relax and not get breast imaging. We cannot ignore the 90% of the population who would otherwise have a false sense of security under the umbrella of "average" risk. 

What about those under 50?

As a general rule, biologically, cancers in younger women tend to grow faster and hence metastasize earlier. The lag period in the time before a lesion is picked up is therefore potentially shorter in women under 50 than in post menopausal women. Some of the cancers seen in screening in those over 50 were actually potentially diagnosable when the patient was under 50 years 9

Criteria for a screening test

There are three stepsnecessary to prove that screening mammography is effective in breast cancer 7:

1. The test can find cancers when they are smaller than without the test: mammography has succeeded here without doubt. To such an extent that "overdiagnosis" is now a concern.

2. randomized, controlled trials must show a reduction in mortality: there is no argument here in the accepted medical literature. Seven trials have demonstrated this 2,7.

3. when the test is introduced into the general population, the death rate declines: the number of deaths per thousand of the population. Screening mammography has reduced the death rate of women 7,8.

OverdiagnosisHistorical background 

Increased survival rates for breast cancer are due in part to earlier diagnosis but also markedly improved treatments. Not only are more women surviving this disease, they are doing it with cosmetically acceptable results. This is partly due to the use of screening mammography. Treated patients may now enjoy a good quality of life without the radical surgical interventions previously used which were often associated with unpleasant sequelae.

The definitioninitial literature support for screening came from the Two Counties Trial in Sweden. Follow up for the trial participants continues and the data support the continued use of overdiagnosisscreening to detect breast cancer at an early stage when the therapy is epidemiologicpotentially curative and cosmetically acceptable. The Two Counties trail and the subsequent Health Insurance Plan (HIP) study in New York showed a decrease in deaths from breast cancer in those aged 40-74 years. A direct result of the HIP study was that screening was introduced in the USA, although it is not pathologic i.eperformed universally on all relevant populations there.

Concepts of risks

As they pertain to screening and breast cancer, there is significant confusion among the general population and many professionals about the concepts of different risks (relative risk, absolute risk and attributable risks).

Most cases of breast cancer are understood to be sporadic. The prevalence of genetic mutations associated with breast cancer such as the BRCA1 and 2 genes varies by population. Although some studies look at the occurrence of breast cancer in people with first degree family history, this does not mean that all of these cases are genetic.

Controversies

  • Age to begin screening: As a cancer wouldgeneral rule, biologically, cancers in younger women tend to grow faster and hence metastasize earlier. The lag period in the time before a lesion is picked up is therefore potentially shorter in women under 50 than in post menopausal women. Some of the cancers seen in screening in those over 50 were actually potentially diagnosable when the patient was under 50 years 9. Nonetheless, on a population basis, in certain contexts, specifically low resource settings, screening populations under 50 is not have been diagnosed duringrecommended 14.  Recommendations vary country by country and across different professional organizations within the same country.
  • Age to stop screening: Although it is currently accepted that screening is not cost effective after a patient's lifetime if screening had not taken placecertain age, as life expectancy rises, the precise age for each population is currently a matter of ongoing research.
  • Overdiagnosis: Unfortunately, there are currently no pathological or imaging features to distinguish the progressive cancers - with lethal potential - from the indolent cases.In general, much overdiagnosis will likely represent cases of low grade DCIS (ductal carcinoma in situ) and those cases of indolent IDC that on review were actually present on mammograms of years ago but have only now been diagnosed for whatever reason (as a general rule, the rate.Some cases of growth of an IDC can be an indication of how aggressive the tumour is).

    All radiologists have seen

    cancers like this: they have been there for years in an invariably elderly lady and they don'tthat are well followed without intervention do not seem to change much with time. Maybe we need to re-evaluate in terms of how we manage confirmed low grade DCIS or small slow growing indolent cancers in elderly patients with multiple comorbidities.they appear on radiological studies available at present. Some breast cancers will not be fatal. Indeed in some autopsy series, up to 2% of female autopsies have breast cancer. But the cancers that will not kill are not only those we find on screening; they also include large palpable cancers 10.

For a comprehensive overview of the current thinking on breast screening, there is a comprehensive review supplement in the Journal of Medical Screening Sept 2012 13.

  • -<p>There are few areas in imaging specifically and medicine in general, fraught with more controversy than <strong>screening for breast cancer</strong>. Due to the emotive issues surrounding the diagnosis, the scientific literature on breast screening and its issues reaches the lay press quickly and is sometimes reproduced in non-scientific, often potentially inaccurate terms. </p><p><a href="/articles/mammography">Mammography</a> is not a perfect study and it does not find all cancers in all women. But until a cure is found, this is currently the best universally available tool we have to find <a href="/articles/breast-neoplasms">breast cancers</a> reliably and reproducibly early in the disease process.</p><h4>The rationale behind screening</h4><p>The rationale behind screening for breast cancer is the universally accepted dictum that (all other factors being equal) earlier diagnosis results in increased survival. The smaller the cancer at the time of diagnosis, the better the 5 year survival of breast cancer.</p><p>In general, if a breast cancer is found at less than a 1 cm diameter, the 5 year survival is the same as the general population at large. Screening for breast cancer is cost and risk effective, feasible and evidence-based.</p><h4>Historical background </h4><p>The increased survival in breast cancer is due in part to earlier diagnosis but also markedly improved treatments. </p><p>The previously used radical surgical therapies for breast cancer are now a thing of the past. <a href="/articles/lymphoedema-1">Lymphoedema</a> used to be a very significant, dreaded complication of <a href="/articles/mastectomy">mastectomy</a> and is now a rare occurrence in clinical practice.</p><p>Not only are more women surviving this disease, they are doing it with cosmetically acceptable results. This is a direct result of the use of screening mammography. Treated patients may now enjoy a good quality of life without the radical surgical interventions previously used which were often associated with unpleasant sequelae.</p><p>The initial literature support came from the Two Counties Trial in Sweden. Follow up for the trial participants continues and the data support the continued use of screening to detect breast cancer at an early stage when the therapy is potentially curative and cosmetically acceptable. The Two Counties trail and the subsequent Health Insurance Plan (HIP) study in New York showed a decrease in deaths from breast cancer in those aged 40-74 years. A direct result of the HIP study was that screening was introduced in the USA.</p><p>Since screening was introduced in the US, the mortality rate from breast cancer has declined by 30%; it had stayed constant from the Second World War.</p><h4>The concept of risk</h4><p>As it pertains to screening and breast cancer, there is significant confusion among the general population and many professionals about the concept of risk.</p><p>Approximately 10% of breast cancers have a first degree family history of breast cancer. This means that 90% or more of the cases will be sporadic, i.e. due to spontaneous mutations in patients with no known family history.</p><p>A common occurrence seen regularly is the reaction when someone is told they have a breast malignancy and invariably the reaction is "but I don't have a family history" or "no one in my family has breast cancer". This unfortunate state of affairs is further compounded by the potentially misleading term "average risk" when used in the context of breast cancer. This is a misnomer. Women with a positive family history are at exceptional risk; women with no family history are at risk because of their gender. The unthinking use of "average risk" inadvertently implies that we should concentrate our efforts at the 10% or that the 90% with no history can somehow relax and not get breast imaging. We cannot ignore the 90% of the population who would otherwise have a false sense of security under the umbrella of "average" risk. </p><h4>What about those under 50?</h4><p>As a general rule, biologically, cancers in younger women tend to grow faster and hence metastasize earlier. The lag period in the time before a lesion is picked up is therefore potentially shorter in women under 50 than in post menopausal women. Some of the cancers seen in screening in those over 50 were actually potentially diagnosable when the patient was under 50 years <sup>9</sup>. </p><h4>Criteria for a screening test</h4><p>There are three steps<strong> </strong>necessary to prove that screening mammography is effective in breast cancer <sup>7</sup>:</p><p>1. The test can find cancers when they are smaller than without the test: mammography has succeeded here without doubt. To such an extent that "overdiagnosis" is now a concern.</p><p>2. randomized, controlled trials must show a reduction in mortality: there is no argument here in the accepted medical literature. Seven trials have demonstrated this <sup>2,7</sup>.</p><p>3. when the test is introduced into the general population, the death rate declines: the number of deaths per thousand of the population. Screening mammography has reduced the death rate of women <sup>7,8</sup>.</p><h4>Overdiagnosis</h4><p>The definition of <a title="Overdiagnosis" href="/articles/overdiagnosis">overdiagnosis</a> is epidemiologic, not pathologic i.e. a cancer would not have been diagnosed during a patient's lifetime if screening had not taken place. Unfortunately, there are currently no pathological or imaging features to distinguish the progressive cancers - with lethal potential - from the indolent cases.</p><p>In general, overdiagnosis will likely represent cases of low grade <a href="/articles/ductal-carcinoma-in-situ">DCIS (ductal carcinoma in situ)</a> and those cases of indolent <a href="/articles/invasive-ductal-carcinoma">IDC</a> that on review were actually present on mammograms of years ago but have only now been diagnosed for whatever reason (as a general rule, the rate of growth of an IDC can be an indication of how aggressive the tumour is).</p><p>All radiologists have seen cancers like this: they have been there for years in an invariably elderly lady and they don't seem to change much with time. Maybe we need to re-evaluate how we manage confirmed low grade DCIS or small slow growing indolent cancers in elderly patients with multiple comorbidities.</p><p>Some breast cancers will not be fatal. Indeed in autopsy series, up to 2% of female autopsies have breast cancer. But the cancers that will not kill are not only those we find on screening; they also include large palpable cancers <sup>10</sup>.</p><p>For a comprehensive overview of the current thinking on breast screening, there is a comprehensive review supplement in the Journal of Medical Screening Sept 2012 <sup>13</sup>.</p>
  • +<p><strong>Screening for breast cancer </strong>includes activities which test members of asymptomatic populations for breast cancer. Many advanced countries have <a href="/articles/breast-screening-programmes">breast screening programs</a>. The most widely adopted method for breast cancer screening is <a href="/articles/mammography">mammography</a>.</p><p>There are few areas in imaging fraught with more controversy than <strong>screening for breast cancer</strong>. Due to the emotive issues surrounding the diagnosis, the scientific literature on breast screening and its issues reaches the lay press quickly and is sometimes reproduced in non-scientific, often potentially inaccurate terms. </p><p>Any screening examination, like any test in medicine, will have a false negative and a false positive rate. Mammography as a screening exam does not find all cancers in all women, and will in some cases be read as positive in women without cancer. Nonetheless mammography is currently believed to the best universally available tool we have to find <a href="/articles/breast-neoplasms">breast cancers</a> reliably and reproducibly early in the disease process.</p><h4>The rationale behind screening</h4><p>The rationale behind screening for breast cancer is the universally accepted dictum that (all other factors being equal) earlier diagnosis results in increased survival.</p><p>Screening for breast cancer is often cost and risk effective, feasible and evidence-based, however cost, risks and treatments available vary dramatically in different populations around the globe.</p><p>There are three steps<strong> </strong>necessary to prove that screening is effective in breast cancer <sup>7</sup>:</p><p>1. The test can find cancers when they are smaller than without the test: mammography has succeeded here without doubt. To such an extent that "overdiagnosis" is now a concern.</p><p>2. randomized, controlled trials must show a reduction in mortality: there is no argument here in the accepted medical literature. Seven trials have demonstrated this <sup>2,7</sup>.</p><p>3. when the test is introduced into the general population, the death rate declines: the number of deaths per thousand of the population. Screening mammography has reduced the death rate of women <sup>7,8</sup>.</p><h4>Historical background </h4><p>Increased survival rates for breast cancer are due in part to earlier diagnosis but also markedly improved treatments. Not only are more women surviving this disease, they are doing it with cosmetically acceptable results. This is partly due to the use of screening mammography. Treated patients may now enjoy a good quality of life without the radical surgical interventions previously used which were often associated with unpleasant sequelae.</p><p>The initial literature support for screening came from the Two Counties Trial in Sweden. Follow up for the trial participants continues and the data support the continued use of screening to detect breast cancer at an early stage when the therapy is potentially curative and cosmetically acceptable. The Two Counties trail and the subsequent Health Insurance Plan (HIP) study in New York showed a decrease in deaths from breast cancer in those aged 40-74 years. A direct result of the HIP study was that screening was introduced in the USA, although it is not performed universally on all relevant populations there.</p><h4>Concepts of risks</h4><p>As they pertain to screening and breast cancer, there is significant confusion among the general population and many professionals about the concepts of different risks (relative risk, absolute risk and attributable risks).</p><p>Most cases of breast cancer are understood to be sporadic. The prevalence of genetic mutations associated with breast cancer such as the BRCA1 and 2 genes varies by population. Although some studies look at the occurrence of breast cancer in people with first degree family history, this does not mean that all of these cases are genetic.</p><h4>Controversies</h4><ul>
  • +<li>
  • +<strong>Age to begin screening</strong>: As a general rule, biologically, cancers in younger women tend to grow faster and hence metastasize earlier. The lag period in the time before a lesion is picked up is therefore potentially shorter in women under 50 than in post menopausal women. Some of the cancers seen in screening in those over 50 were actually potentially diagnosable when the patient was under 50 years <sup>9</sup>. Nonetheless, on a population basis, in certain contexts, specifically low resource settings, screening populations under 50 is not recommended<sup> 14</sup>.  Recommendations vary country by country and across different professional organizations within the same country.</li>
  • +<li>
  • +<strong>Age to stop screening</strong>: Although it is currently accepted that screening is not cost effective after a certain age, as life expectancy rises, the precise age for each population is currently a matter of ongoing research.</li>
  • +<li>
  • +<strong>Overdiagnosis</strong>: Unfortunately, there are currently no pathological or imaging features to distinguish the progressive cancers - with lethal potential - from the indolent cases. In general, much overdiagnosis will likely represent cases of low grade <a href="/articles/ductal-carcinoma-in-situ">DCIS (ductal carcinoma in situ)</a> and those cases of indolent <a href="/articles/invasive-ductal-carcinoma">IDC</a> that on review were actually present on mammograms of years ago but have only now been diagnosed for whatever reason.Some cases of cancers that are well followed without intervention do not seem to change much with time in terms of how they appear on radiological studies available at present. Some breast cancers will not be fatal. Indeed in some autopsy series, up to 2% of female autopsies have breast cancer.</li>
  • +</ul><p> </p>

References changed:

  • 14. WHO Position Paper on Mammography Screening. Geneva: World Health Organization; 2014. Available from: https://www.ncbi.nlm.nih.gov/books/NBK269545/

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