Trial ID # | NCT03596281; PEMBOV |
Phase | I |
Drug Class | Angiogenesis Inhibitors: VEGF |
Drug Name | Bevacizumab |
Alternate Drug Names | immunoglobulin G1 (human-mouse monoclonal rhuMab-VEGF gamma-chain, anti-VEGF monoclonal antibody, Avastin |
Drugs in Trial | Liposomal doxorubicin, Pembrolizumab, Bevacizumab |
Eligible Participant | Platinum resistant or refractory ovarian cancer |
Patients Enrolled | Bev+Pem: 19 patients, 68% w/ prior Bev; 95% w/ 2 or more prior therapies; Bev+PLD+Pem: 22 patients, median 3 prior therapies (1-13), 41% primary Pt-R, 82% w/ prior Bev, 41% w/ prior PARPi |
Therapy Setting | Recurrence |
Study Design | Open-Label, Non-randomized |
Endpoints | CBR, ORR, DCR, evaluated per RECIST |
Efficacy | Bev+Pem: Bev+PLD+Pem: |
Conclusion | Bevacizumab+pembrolizumab with or without liposomal doxorubicin is well tolerated and demonstrate durable responses in platinum resistant ovarian cancer patients |
Reference | Michels J et al. Pembrolizumab and bevacizumab in platinum resistant epithelial ovarian cancer patients. SITC (2021) abstract 355 Michels J et al. PemBOv trial: Pembrolizumab plus bevacizumab with or without pegylated liposomal doxorubicin-based chemotherapy in patients with platinum-resistant ovarian cancer. J Clin Oncol 40, 2022 (suppl 16; abstr 5575) Michels J et al. Poster |