PI3K/ AKT/mTOR Pathway Inhibitors in the Treatment of HR+/HER2- Metastatic Breast Cancer – Enduring Webcast
Description
Program Description
This enduring webcast will provide up-to-date, evidence-based information for diagnosing and treating patients with HR+/HER2–Â metastatic Breast Cancer. The activity will focus on:
HR+/HER2—MBC Testing: Hybrid capture-based next generation sequencing (NGS) assays (FoundationOne®, FoundationOne®CDx, or FoundationOne®Liquid CDx) CLIA-certified, College of American Pathologists (CAP)-accredited laboratory (Foundation Medicine, Inc.) -Guideline update
- Comprehensive Genomic Profiling of ESR1, PIK3CA, AKT1, and PTEN in HR+/HER2—MBC.
HR+/HER2— MBC – First-line CDK4/6i combinations for HR+/HER2—MBC with PIK3CA mutation (PIK3CAmt)
- Palbociclib plus fulvestrant versus placebo plus fulvestrant
- Abemaciclib plus fulvestrant versus placebo plus fulvestrant
HR+/HER2—MBC – Second-line therapies for HR+/HER2—MBC with PIK3CA/AKT1/PTEN alterations
- After progression on endocrine therapy plus CDK4/6i, second-line options for patients with PIK3CA/AKT1/PTEN alterations include inavolisib, alpelisib, capivasertib, and everolimus.
- Investigational therapies for HR+/HER2—MBC with PIK3CA/AKT1/PTEN alterations – Gedatolisib
- Mutant-selective inhibitors – RELAY 2608, STX-478, LOXO-783, TOS-358
Adverse Effects (AEs)Â – Management of associated toxicities with the inhibitors of the PI3K/AKT/mTOR pathway
- Hyperglycemia and Hyperinsulinemia
- Stomatitis
- Maculopapular Rash
- Cardiovascular Events (CVAEs)
Intended Audience
Medical oncologists, pathologists, nurse practitioners, physician assistants, and nurses who diagnose and treat patients with HR+/HER2– metastatic Breast Cancer.
Commercial Supporter
This activity is supported by an educational grant from AstraZeneca Pharmaceuticals
CME | 1.25 Credits
Webcast
Time to Complete: 75 minutes
Released: October 3, 2025
Expires: October 3, 2026
Maximum Credits:
1.25 / AMA PRA Category 1 CreditsTM
1.25 / ANCC Contact Hours