A Multicenter, Observational Study on the Real-World Effectiveness and Safety of inavolisib Combined with Endocrine Therapy With or Without a CDK4/6 Inhibitor in Patients with HR-Positive/HER2-Negative, PIK3CA-Mutated Advanced Breast Cancer.
Study Type
OBSERVATIONAL
Enrollment
100
Inavolisib in Combination With ET
Inavolisib in Combination With ET+CDK4/6i
Real-World Progression-Free Survival (rwPFS)
Time from the index date (first prescription of inavolisib) to the first recorded disease progression (based on radiological or clinical assessment) or death from any cause, whichever occurs first.
Time frame: From first prescription of inavolisib to disease progression or death from any cause, assessed for up to approximately 3 years
Stratified rwPFS for Cohort A and Cohort B
Time from the index date (first prescription of inavolisib) to the first recorded disease progression (based on radiological or clinical assessment) or death from any cause, whichever occurs first.
Time frame: From first prescription of inavolisib to disease progression or death from any cause, assessed for up to approximately 3 years
Number of Participants With Adverse Events (AEs)
Time frame: Up to approximately 36 months
Real-world Duration of Response (rwDoR)
Time frame: From onset of first tumor response to first occurrence of PD or death from any cause (up to approximately 36 months)
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