Trial ID # | NCT02657889; TOPACIO |
Phase | I/II |
Drug Class | Immunotherapy: Checkpoint Inhibitors/PD-1 |
Drug Name | Pembrolizumab |
Alternate Drug Names | Keytruda, Lambrolizumab, SCH 900475, MK3475, MK-3475 |
Drugs in Trial | Pembrolizumab, Niraparib |
Eligible Participant | Platinum resistant, refractory or sensitive (platinum-ineligible) ovarian cancer with ≤ 5 prior therapies; no primary Pt-R/Pt-Rf |
Patients Enrolled | 62; median 3 prior therapies (1-5) (Phase I: 9, Phase II: 53); 63% w/ prior Bev |
Therapy Setting | Recurrence |
Study Design | Open-Label, Non-randomized |
Endpoints | ORR, DCR, PFS, evaluated per RECIST |
Biomarkers | Exploratory: BRCA1/2, HRD (myChoice HRD test, Myriad Genetics), PD-L1 protein |
Efficacy | ORR: 18.3% (3CR, 8PR, n=60) Exploratory analysis Pt status: 5 of 8 patients with long-term response (>6 months) were Pt-R/Pt-Rf and BRCA WT |
Clinically Significant Adverse Events | Serious AE: none |
Conclusion | Promising activity of non-chemotherapy combination in Pt-R/Pt-Rf patients independent of BRCA status, HRD status and PD-L1 expression |
Reference | Konstantinopoulos PA et al. TOPACIO/Keynote-162 (NCT02657889): A phase 1/2 study of niraparib + pembrolizumab in patients (pts) with advanced triple-negative breast cancer or recurrent ovarian cancer (ROC)—Results from ROC cohort. J Clin Oncol (2018) 36 (suppl; abstr 106) Konstantinopoulos PA et al. Single-Arm Phases 1 and 2 Trial of Niraparib in Combination With Pembrolizumab in Patients With RecurrentPlatinum-Resistant Ovarian Carcinoma. JAMA Oncol (2019) 5(8):1141-1149 |