Evaluating the Performance of AI in Evaluating Breast MRI Performed With Dose Reduction

The study involves each patient presenting for an initial MRI with a regular dose of gadolinium and then presenting at least 48 hours after (no less than 14 days later) for a ¼ dose (see below regarding dosing) gadolinium MRI exam. Both exams will be performed on a 1.5 Tesla magnet. Both exams will include a full protocol. The full dose contrast exam will be read as standard protocol. All images will be anonymized. Images from the reduced dose study will be collected and an AI algorithm applied. All three anonymized data sets (regular dose, low dose, and AI algorithm applied to low dose) will be provided to the readers.

Readers will be three attending radiologists specializing in breast imaging. Exams will be scored on quality, background parenchymal enhancement (BPE), and lesion conspicuity. Enhancing lesions will be identified and characterized by the radiologists in a document provided.

Inclusion criteria

for Breast Cancer Patients:

• Female patient between ≥ 18 years old and ≤ 99 years old
• Patients with newly diagnosed primary breast cancer
• Patient able and willing to participate in the trial

Inclusion criteria

for Non-malignant indications:

• Female patients between ≥ 18 years old and ≤ 99 years old
• Be referred for MRI for non-malignant indications (screening or BIRADS 3)
• Patients have had prior exam with known enhancing mass, nonmass enhancement, or focus/foci.

Exclusion criteria

• Non-female patients
• Patients < 18 years old
• Women who are lactating or pregnant
• Patients with recurrent breast cancer
• Patients who have already received neoadjuvant chemotherapy
• Unable to lie still on the imaging table for one (1) hour
• Patients that are unable to undergo MRI evaluation for reasons specific to MRI