Emerging Horizons in Ovarian Cancer Exploiting Pathways of Susceptibility
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.
FDA-Approved Drugs for Ovarian Cancer
FDA-Approved PARP Inhibitors
Cellular DNA Repair Pathways
PARP Trapping
Phase 3 PARP Inhibitor Maintenance Studies
SOLO2/ENGOT-OV21: Olaparib vs Placebo as Maintenance Therapy After Platinum-Based Treatment, Phase 3
ENGOT-OV16/NOVA: Niraparib vs Placebo as Maintenance Therapy After Platinum-Based Treatment, Phase 3
ARIEL3: Rucaparib vs Placebo as Maintenance Therapy After Platinum-Based Treatment, Phase 3
Quality-Associated PFS With Olaparib, SOLO2
Time Without Symptoms of Disease or Toxicity (TWiST)
Mechanisms of Resistance to PARP Inhibitors
Enhancing Anti-Tumor Activity Combining PARPi’s with Other Targeted Therapies
Potential Overlap of DNA Repair and Angiogenic Pathways
PARPi Plus Anti-Angiogenic Therapy Olaparib + Cediranib, Phase 2
PARPi Plus Anti-Angiogenic Therapy Olaparib + Cediranib, Ongoing Studies
PARPi Plus Anti-Angiogenic Therapy Niraparib + Bevacizumab
PARPi Plus Checkpoint Inhibitors Durvalumab + Olaparib or Cediranib, Phase 1
PARPi Plus Checkpoint Inhibitors Niraparib + Pembrolizumab, Ongoing Phase 1/2
PARPi Plus Checkpoint Inhibitors Ongoing Clinical Trials
Other Combination Therapy
PARPi Plus Chemotherapy Veliparib + Carboplatin/Paclitaxel, Ongoing Phase 3
Key Takeaways
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