Table 1.
All patients (n=16) |
Chemo+TIL (n=13) |
Chemo+TIL+IFNa (n=3) | |
Age | |||
Median age and range (year) | 61 (29–77) | 62 (29–77) | 58 (53–73) |
WHO status; n (%) | |||
0 | 6 (38) | 6 (46) | 0 (0) |
1 | 10 (62) | 7 (54) | 3 (100) |
2 | 0 (0) | 0 (0) | 0 (0) |
Tumor type | |||
HGSOC | 15 (94) | 12 (92) | 3 (100) |
LGMOC | 1 (6) | 1 (8) | 0 (0) |
Platinum sensitivity | |||
>6 and <12 months | 6 (38) | 5 (38) | 1 (33) |
>12 months | 10 (62) | 8 (62) | 2 (67) |
Mutation status; n (%) | |||
BRCA mutation | 2 (13) | 2 (15) | 0 (0) |
HR status; n (%) | |||
ER− and PrR− | 4 (25) | 3 (23) | 1 (33) |
ER+ or PrR+ | 7 (44) | 6 (46) | 1 (33) |
Unknown | 5 (31) | 4 (31) | 1 (33) |
Previous lines of chemotherapy; n (%) | |||
1 | 12 (75) | 10 (77) | 2 (67) |
2 | 3 (19) | 2 (15) | 1 (33) |
>3 | 1 (6) | 1 (8) | 0 (0) |
Other previous treatments; n (%) | |||
Bevacizumab | 2 (13) | 1 (8) | 1 (33) |
Endocrine therapy | 2 (13) | 1 (8) | 1 (33) |
PARPi | 2 (13) | 1 (8) | 1 (33) |
ER, estrogen receptor; HGSOC, high grade serous ovarian cancer; HR, hormone receptor; LGMOC, low-grade mucinous ovarian cancer; PrR, progesterone receptor.