Table 1.
Variable | N = 476 |
---|---|
Cancer type | |
Epithelial ovarian cancer | 386 (81%) |
Fallopian tube cancer | 43 (9%) |
Primary peritoneal cancer | 47 (10%) |
Histological classification | |
Serous | 449 (94%) |
Others | 27 (6%) |
Platinum-sensitivity of the recurrent disease | |
Sensitive | 299 (63%) |
Resistant | 138 (29%) |
Refractory | 39 (8%) |
BRCA mutational status | |
BRCA1 | 117 (25%) |
BRCA2 | 57 (12%) |
BRCA wild-type | 302 (63%) |
Homologous recombination deficiency (HRD) status | |
BRCA1 mutation | 117 (25%) |
BRCA2 mutation | 57 (12%) |
BRCA, wild type LOH-high | 126 (26%) |
BRCA, wild type LOH-low | 152 (32%) |
BRCA, wild type LOH(unknown) | 24 (5%) |
Best radiological response after 100 days according to RECIST criteria | |
Complete response | 23 (5%) |
Partial response | 125 (26%) |
Stable disease | 141 (30%) |
Progressive disease | 63 (13%) |
Not evaluable | 124 (26%) |
CA-125 response according to the GCIG | |
Unfavorable | 175 (37%) |
Favorable | 107 (22%) |
Not evaluablea | 194 (41%) |
Key outcome measures | |
Platinum-sensitive cohort (n = 299) | |
Best subsequent radiological response | |
Complete response | 21 (7%) |
Partial response | 96 (32%) |
Stable disease | 92 (31%) |
Progressive disease | 37 (12%) |
Not evaluable | 53 (18%) |
Progression-free survival (PFS) with a 100 day landmark | 5.3 [4.1–6.00] |
Platinum-resistant cohort (n = 177) | |
Best subsequent radiological response | |
Complete response | 2 (1%) |
Partial response | 29 (16%) |
Stable disease | 49 (28%) |
Progressive disease | 26 (15%) |
Not evaluable | 71 (40%) |
Progression-free survival (PFS) with a 100 day landmark | 4.1 [4.0–5.5] |
LOH: loss-of-heterozygosity.
CA-125 response according to the GCIG: baseline CA-125 not available or baseline <2 N (70 kU/L).