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. 2021 Jan 15;10:604084. doi: 10.3389/fonc.2020.604084

Table 2.

Published clinical trials of immunotherapies modulating adaptive immunity of ovarian cancer patients.

Intervention NCT/Author Phase Enrollment Primary Endpoint PFS OS ORR
CAR-T
 Anti-Folate Receptor Kershaw et al. 1 14 recurrent FR+ OC Safety and Activity *
 Anti-Mesothelin Beatty et al. 1 5 OC Safety and Activity 0/5
Anti-CTLA4
 Ipilimumab Hodi et al. 1 9 Stage 4 OC Safety and Activity 0/9
NCT01611558 2 40 RPS OC DrAEs 4/39 (10.3%)
 Nivolumab+Ipilimumab Zamarin et al.
NCT02498600
2 100 recurrent OC ORR 3.9 months 28.1 months 16/51 (31.4%)
Anti-PD-1
 Nivolumab Hamanishi et al. 2 20 RPR OC Safety and Activity 3.5 months 20.0 months 3/20 (15%)
 Nivolumab + Bevacizumab Liu et al. 2 38 recurrent OC ORR 12.1 months in RPS
7.7 months in RPR
8/20 (40%) in RPS
3/18 (16.7%) in RPR
 Pembrolizumab Varga et al. 1b 26 PD-L1+ OC ORR 1.9 months 13.8 months 3/26 (11.5%)
 Pembrolizumab Matulonis et al. 2 Cohort A: 285 recurrent OC
Cohort B: 91 recurrent OC
ORR Cohort A: 2.1 months
Cohort B: 2.1 months
Cohort A: -
Cohort B: 17.6 months
Cohort A: 7.4%
Cohort B: 9.9%
 Pembrolizumab + Niraparib Konstantinopoulos et al. 1/2 Phase 1: 9 RPR OC
Phase 2: 53 RPR OC
Phase 1: Safety and RP2D
Phase 2: ORR
3.4 months Integrated: 18%
 Durvalumab + Olaparib +  Cediranib Zimmer et al. 1 7 recurrent OC
1 peritoneal cancer
1 endomterial
1 TNBC
RP2D 4/9 (44%)
 Durvalumab + Olaparib Lampert et al. 2 35 recurrent OC ORR 3.9 months 5/35 (14%)
 Durvalumab + Olaparib Drew et al. 2 32 BRCAmut, RPS OC ORR 20/32 (63%)
Anti-PD-L1
 Avelumab Disis et al.
NCT01772004
1b 125 recurrent OC ORR 2.6 months 11.2 months 12/125 (9.6%)

-Not reported; *No patients responded to treatment; RPR, recurrent platinum-sensitive; RPR, recurrent platinum-resistant; RP2D, Recommended phase 2 dose; TNBC, Triple-negative breast cancer; ORR, Overall response rate.