This observational disease registry is a prospective, national, non-interventional study designed to enroll participants who have received an initial diagnosis of unresectable, locally advanced (LA) or metastatic breast cancer (mBC), up to 6 months prior to registry enrolment. These participants will be prospectively followed for at least 5 years after study enrolment to evaluate their anti-cancer treatments. Data on participants' previous anti-cancer treatments for breast cancer will be collected retrospectively at study entry.
Study Type
OBSERVATIONAL
No intervention was administered in this study.
Progression-Free Survival (PFS) For Each Anti-Cancer Treatment Regimen
Time frame: Up to approximately 8 years
Overall Survival (OS)
Time frame: Up to approximately 8 years
Objective Response Rate (ORR) For Each Anti-Cancer Treatment Regimen
Time frame: Up to approximately 8 years
Number and Percentage of Participants Receiving Each Unique Treatment Regimen Overall and as First-Line Therapy Versus Second-Line Therapy Versus Subsequent-Line Therapy
Time frame: Up to approximately 8 years
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