Clinical Research Directory

Inclusion Criteria: * -Female patients aged ≥18 years old at the time of T-DXd initiation * Patients with a confirmed histological or cytologically based diagnosis of HR-positive mBC. * Patients who were classified as HER2-low or HER2-ultralow mBC confirmed by the closest locally obtained HER2 test prior to or on the index date, and who meet the following definitions: * HER2-low status defined as IHC scores 1+ and 2+ without ISH gene amplification based on the pathology report. * HER2-ultralow status defined as IHC 0 with membrane staining based on the pathology report. * Patient who received at least one prior line of ET (± targeted therapy) in the metastatic setting. * Patients who are chemotherapy-naïve in the metastatic setting. * Patients who initiated T-DXd up to 30 days before the signature of the ICF. The decision to initiate T-DXd must be made independently by treating physicians as part of routine clinical practice. * Patients are willing to sign the written ICF, indicating that they understand the purpose of the study and procedures required for participation. Exclusion Criteria: * -Patients with a history of other malignancies, other than basal cell carcinoma of the skin and squamous cell carcinoma of the skin. * Patients who received prior chemotherapy in the metastatic setting. * Patients with Eastern Cooperative Oncology Group (ECOG) status ≥2 or missing ECOG status at the time of initiation of T-DXd (index date). * Patients with a history of participation in another clinical trial in the metastatic setting. * Female patient with current or planned pregnancy, or breastfeeding.