The Use of PARP Inhibitors in Breast Cancer: Challenges and Opportunities
This program will include a discussion of off-label treatment and investigational agents not approved by the FDA for use in the United States and data that were presented in abstract form. These data should be considered preliminary until published in a peer-reviewed journal.
PARP and PARP Inhibition
PARP Inhibitors Studied in Breast Cancer
BROCADE 2: Study Design
BROCADE 2: Results
I-SPY2: Veliparib/Carboplatin Graduates
BrighTNess: TNBC and Continuous Dosing
BrighTNess Efficacy Data
Phase 2 Studies of Olaparib in gBRCA+ MBC
ABRAZO: Talazoparib Phase 2 in gBRCA+ MBC
OlympiAD Study Design
Primary Endpoint: PFS by BICR
Time to Second Progression or Death (PFS2) by Investigator Assessment
OS: Interim Analysis (46% Data Maturity)
Objective Response by BICR
ORRs in Subgroups
OlympiA Study Population
OlympiA: Methodology
Pilot Study of Neoadjuvant Talazoparib For Early-Stage BRCA+ Breast Cancer
Pilot Study of Neoadjuvant Talazoparib For Early-Stage BRCA+ Breast Cancer (cont)
OlympiAD: AEs
OlympiAD: AEs (cont)
Ongoing Questions
Assays for “BRCAness”/HRD
Mechanisms of Resistance to PARP Inhibitors
Abbreviations
Abbreviations (cont)
Abbreviations (cont)