Prospective Registry of ADC as First- and Second-line Treatment for Breast Cancer

Inclusion Criteria

• Male or female patients aged 18 years or greater with ability to provide written informed consent for this prospective registry study.
• Estimated life expectancy of at least at 3 months per investigator assessment.
• Willingness to provide an archival tissue sample and blood samples (20cc research blood collection at several timepoints) for research purposes.
• Cohort-specific enrollment criteria:

• Cohort 1: Histologically documented HR+/HER2- MBC with plan to start an FDA-approved ADC as their first ADC per standard of care (SOC).
• Cohort 2: Histologically documented metastatic TNBC with plan to start an FDA-approved ADC as their first ADC per standard of care
• Cohort 3: Histologically documented HR+/HER2- MBC with plan to start an FDA-approved ADC as their second ADC per standard of care (ADC1 should be an approved ADC administered per SOC or as monotherapy in a clinical trial; no prior experimental ADCs allowed). Clinical data from the first ADC must be available for retrospective review.
• Cohort 4: Histologically documented metastatic TNBC with plan to start an FDA-approved ADC as their second ADC per standard of care (ADC1 should be an approved ADC administered per standard of care or as monotherapy in a clinical trial; no prior experimental ADCs allowed). Clinical data from the first ADC must be available for retrospective review.
• Measurable disease is not required for any cohort.

Exclusion Criteria

• Prior receipt of an experimental ADC in the metastatic setting. Of note, patients who received an FDA-approved ADC as their first ADC (as monotherapy, not in combination) can participate in cohorts 3 or 4 prior to starting their second FDA-approved ADC per standard of care. Of note, for all cohorts, experimental therapies are not allowed as intervening therapies after starting ADC1. If a patient enrolls on a clinical trial of an experimental therapy after ADC1, they will be taken off study.
• Current participation in a clinical trial with an ADC.
• Contraindication to research phlebotomy to collect \~20cc blood at each research blood draw timepoint.