MRI + Mammography for Breast Cancer Screening
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to determine how well two screening methods—abbreviated breast MRI and digital tomosynthesis mammography (also known as Digital Breast Tomosynthesis or 3D Mammography)—detect breast cancer in women with dense breasts. The trial will assess whether combining these methods yields better results than using just one. Women with dense breast tissue who are not experiencing symptoms or undergoing other breast cancer treatments qualify as good candidates for this study. Participants will undergo both screening methods either on the same day or within 24 hours, both at the start and after one year. As an unphased study, this trial offers participants the chance to contribute to important research that could enhance breast cancer detection methods.
Will I have to stop taking my current medications?
The trial does not specify if you need to stop taking your current medications, but you cannot be taking medication for breast cancer prevention.
What prior data suggests that this screening method is safe for women with dense breasts?
Research has shown that abbreviated breast MRI is generally safe and well-tolerated. It accurately and quickly detects breast cancer, with no major safety concerns reported. This method uses radio waves and magnets to create detailed images, without any radiation.
Studies indicate that digital tomosynthesis mammography is also safe and effective. It uses X-rays to create 3D images of the breast, which can help find cancer more accurately, especially in dense breast tissue. Reports suggest it has fewer side effects and requires fewer follow-up tests than traditional mammography.
Both methods are designed for regular use and have proven effective in detecting breast cancer.12345Why are researchers excited about this trial?
Researchers are excited about this trial because it combines Abbreviated Breast MRI (AB-MR) and Digital Tomosynthesis Mammography (DBT) for breast cancer screening, potentially enhancing early detection. Unlike traditional mammography, DBT provides a 3D image of the breast, improving accuracy and reducing false positives. Meanwhile, AB-MR is a quicker version of the standard MRI, taking less than 10 minutes, which makes it more accessible and less time-consuming for patients. By exploring the effectiveness of using these techniques together, researchers hope to improve screening accuracy and provide a more comprehensive assessment of breast health.
What evidence suggests that MRI and mammography are effective for breast cancer screening in women with dense breasts?
This trial compares the effectiveness of two breast cancer screening methods: Abbreviated Breast MRI (AB-MR) and Digital Tomosynthesis Mammography (DBT). Studies have shown that a shorter version of breast MRI effectively detects breast cancer, correctly identifying cancer in up to 94.7% of cases. Research also indicates that this method can find more invasive cancers compared to some other imaging techniques. Meanwhile, digital tomosynthesis mammography, which creates 3D pictures of the breast, finds more cancers and has fewer false alarms than traditional 2D mammography. This trial will test the combination of both methods, potentially offering a better screening option for women with dense breast tissue by detecting more cases of cancer early. Participants in Arm A will undergo DBT followed by AB-MR, while those in Arm B will undergo AB-MR followed by DBT.23567
Who Is on the Research Team?
Christopher Comstock
Principal Investigator
ECOG-ACRIN Cancer Research Group
Are You a Good Fit for This Trial?
This trial is for women with dense breasts who are due for routine screening, not pregnant or breastfeeding, and have no history of breast cancer or high-risk lesions. They mustn't be taking breast cancer prevention drugs, haven't had a breast MRI before, and can undergo an MRI with contrast. Women at high risk for breast cancer or those with certain health conditions like severe allergies to gadolinium or renal impairment are excluded.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Baseline Testing
Participants undergo DBT and AB-MR on the same day or within 24 hours
1-Year Follow-up Testing
Participants undergo follow-up DBT and AB-MR after 1 year
Long-term Follow-up
Participants are monitored every 6 months for 3 years after the study completion
What Are the Treatments Tested in This Trial?
Interventions
- Abbreviated Breast MRI
- Digital Tomosynthesis Mammography
Find a Clinic Near You
Who Is Running the Clinical Trial?
ECOG-ACRIN Cancer Research Group
Lead Sponsor
National Cancer Institute (NCI)
Collaborator