FDA Finalizes New Mammography Dense Breast Notification Rule
SUMMARY:
The FDA has updated the mammography regulations and now requires that mammography facilities notify patients about the density of their breasts. The amendments incorporate language that specifies how breast density can influence the accuracy of mammography in addition to recommending a discussion with their healthcare professional. The rule goes into effect September 10, 2024. Currently, the ACOG committee opinion states unequivocally that healthcare professionals comply with all laws, although evidence is lacking as to clinical utility and improved outcomes with additional screening and testing.
Summary of Results to be Provided to Patients (FDA Rule)
Non-Dense Breast
Breast tissue can be either dense or not dense
Dense tissue makes it harder to find breast cancer on a mammogram and also raises the risk of developing breast cancer
Your breast tissue is not dense
Talk to your healthcare provider about breast density, risks for breast cancer, and your individual situation
Dense Breast
Breast tissue can be either dense or not dense
Dense tissue makes it harder to find breast cancer on a mammogram and also raises the risk of developing breast cancer
Your breast tissue is dense
In some people with dense tissue, other imaging tests in addition to a mammogram may help find cancers
Talk to your healthcare provider about breast density, risks for breast cancer, and your individual situation
ACOG
The current ACOG Practice Advisory States
While ACOG does not recommend routine use of alternative or adjunctive tests to screening mammography in individuals with dense breasts who are asymptomatic and have no additional risk factors, ACOG recommends that clinicians comply with the new FDA rule and any state laws and federal rules that require disclosure of a patient’s breast density as recorded in a mammogram report
BI-RADS Density Categories (for more on BI-RADS classification, see ‘Related ObG Topics’ Below)
a. Breasts are almost entirely fatty
Prevalence: 10%
Mammography considered highly sensitive in this setting (88%)
b. There are scattered areas of fibroglandular density
Prevalence: 43%
Still sensitive but decreased from category a (82%)
c. Breasts are heterogeneously dense
Prevalence: 39%
Small masses may be obscured
Sensitivity drops to 69%
d. Breasts are extremely dense
Prevalence: 8%
Significantly lowers sensitivity of mammography (62%)
KEY POINTS:
Dense breast tissue and screening is more common in younger women
Accuracy of mammography for the detection of breast cancer is reduced (less sensitive)
In women with heterogeneously and extremely dense breasts, digital mammography appears to be superior to film with respect to efficacy
Breast cancer risk
Dense breast tissue (BI-RADS density categories c and d) is associated with increased breast cancer risk
BI-RADS c breast cancer risk: 1.2 relative risk compared to average breast density
BI-RADS d breast cancer risk: 2.1 relative risk compared to average breast density
The FDA also has required reporting language that should be provided to the referring healthcare professional that falls into 4 categories
(A) The breasts are almost entirely fatty
(B) There are scattered areas of fibroglandular density
(C) The breasts are heterogeneously dense, which may obscure small masses
(D) The breasts are extremely dense, which lowers the sensitivity of mammography
BI-RADS: Standardizing Breast Imaging and Reporting
WHAT IS IT?
BI-RADS: Breast Imaging Reporting and Data System, was developed by the American College of Radiology (ACR) to standardize mammogram reporting, as well as breast ultrasound and MRI reporting.
The standard mammogram report includes the following
Indication and type of mammogram (screening/diagnostic)
Statement regarding breast density
Description of pertinent findings including size and location, oriented by quadrant and clock position
Summary of important findings and BI-RADS category
KEY POINTS:
BI-RADS Classification Standardizes Findings and Recommendations for Further Management
BI-RADS 0 : Incomplete
Recall for additional imaging/comparison with prior examinations, or both
BI-RADS 1: Negative (Essentially 0% chance of malignancy)
Routine screening
BI-RADS 2: Benign (Essentially 0% likelihood of malignancy)
Routine screening
BI-RADS 3: Probably benign (> 0% but ≤ 2% likelihood of malignancy)
6 month follow-up or continued surveillance
BI-RADS 4: Suspicious (> 2% but < 95% likelihood of malignancy)
4A: Low suspicion for malignancy (> 2% to ≤ 10% likelihood)
4B: Moderate suspicion for malignancy (> 10% to ≤ 50% likelihood)
4C: High suspicion for malignancy (> 50% to < 95% likelihood)
Tissue diagnosis needed for all BI-RADS 4 categories
BI-RADS 5: Highly suggestive of malignancy (95% likelihood of malignancy)
Tissue diagnosis needed
BI-RADS 6: Known, biopsy proven malignancy
Surgical excision when appropriate
Density Categories
Category a: Breasts are almost entirely fatty
Prevalence: 10% of the population
Mammography considered highly sensitive in this setting (88%)
Category b: There are scattered areas of fibroglandular density
Prevalence: 43% of the population
Still sensitive but decreased from category a (82%)
Category c: Breasts are heterogeneously dense
Prevalence: 39%
Small masses may be obscured
Sensitivity drops to 69%
Note: Breast cancer risk is 1.2 relative risk compared to average breast density
Category d: Breasts are extremely dense
Breasts are extremely dense
Significantly lowers sensitivity of mammography (62%)
Note: Breast cancer risk is 2.1 relative risk compared to average breast density
Professional organizations continue to release evidence-based guidance on mammography, with ACP the latest to provide updated recommendations. While required frequency and starting age may differ, they all emphasize shared decision making with patients, which entails counseling about uncertainty, risk/benefit, and related patient values.
BENEFITS OF MAMMOGRAPHY
Appears to decrease breast cancer mortality by 15 to 20%
Studies demonstrate varying magnitude
ACS (RCT data): Relative risk 0.80-0.82
Recent data from the Canadian National Breast Screening Study did not show decrease when comparing mammography to controls, perhaps due to more recent improvements in treatments but does not take in to account advances in imaging
May increase life expectancy (ACS systematic review) but could not quantitate
HARMS OF MAMMOGRAPHY
False Positives (additional images and benign biopsies)
USPSTF review
Collaborative modeling data: Screening biennially from ages 40 to 74 years would result in 1376 false-positive results per 1000 women screened over a lifetime of screening
ACS review
Increased risk of false positive with dense breasts among women 40-49
Callbacks minimized if prior films available
Anxiety and Distress
May persist even if follow-up is normal
Financial concerns as patient may be responsible for paying for additional tests
Overdiagnosis and Overtreatment
Overdiagnosis is defined as detecting a cancer that would have remained indolent and not become apparent without screening
Overtreatment is defined as treatment for an overdiagnosed cancer
Difficult to discern actual number of overdiagnosed cancers
Collaborative modeling data (USPSTF): Screening biennially from ages 40 to 74 years would lead to 14 overdiagnosed cases of breast cancer per 1000 persons screened over the lifetime of screening with a very wide range of estimates (4 to 37 cases) across models
Other organizations such as ACS make the point that certain assumptions may not be verifiable in addition to bias in methodology and design
PROFESSIONAL GUIDELINES:
ACOG
Start Age
Recommend at age 40
Screening Interval
Every 1 or 2 years (shared decision-making)
Stop Age
Age 75
> 75 shared decision-making including overall health and longevity
USPSTF
Start Age
Recommend at 40 years
Screening Interval: Every 2 years until 74 years
Stop Age
≥ 75 years: Insufficient evidence to recommend for/against
ACS
Start Age
Recommend at age 45 years | Consider 40 years if patient desires
Screening Interval
45 – 50 years: annual
≥55 years: Every 2 years or can choose annual
Stop Age
Continue if good health and life expectancy >10 years
ACR
Start Age
Recommend at 40 years
Screening Interval: Annual
Stop Age
“Screening should continue past age 74 without an upper age limit, unless severe comorbidities limit life expectancy or ability to accept treatment.“
Note: ACR updated guidelines to include transgender patients stating “Annual screening at age 40 is recommended for transfeminine (male-to-female) patients who have used hormones for ≥5 years, as well as for transmasculine (female-to-male) patients who have not had mastectomy”
ACP
Start Age
Recommended at 50 years
40-49 years: Discuss risks vs benefits and patient preference (“potential harms outweigh the benefits for most women” in this age bracket )
Screening Interval: Every 2 years
Stop Age
Screening not recommended for women ≥75
Life expectancy ≤10 years
NCCN
Start Age
Recommend at 40 years
Screening Interval: Annual
Stop Age
Upper age limit not yet established
Consider comorbidities that may impact life expectancy (≤10 years)
American Society of Breast Surgeons
Start Age
Non-dense breasts (A and B density): 3D preferred modality | Age 40 | No need for supplemental imaging
Dense breasts (C and D density): 3D preferred modality | Age 40 | Consider supplemental imaging
Screening Interval
Annual
Stop Age
When life expectancy is <10 years
ADDITIONAL KEY POINTS:
Clinical Breast Examination (CBE)
ACOG & NCCN: Offer every 1 to 3 years for women 25 to 39 years and annually for ≥ 40 years
USPSTF & AAFP: Insufficient evidence to recommend for or against
ACS, ACP & Canadian Task Force on Preventative Healthcare: Not recommended
WHO: CBE may be of benefit for women age 50 to 69 years with poor access to healthcare resources
Most professional organizations find insufficient evidence to recommend adjunctive screening using breast ultrasonography, MRI, Digital Breast Tomosynthesis, or other method in the setting of a normal mammogram and no other risk factors
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