Characteristics | Group A | Group B | |||
---|---|---|---|---|---|
n = 44 | n = 33 | p-Value | |||
Age (years) | 0.07 | ||||
Median (range) | 54 | (30–77) | 61 | (29–77) | |
FIGO stage (%) | 0.03 | ||||
I | 2 | (4.5) | 7 | (21.2) | |
II | 4 | (9.1) | 3 | (9.1) | |
III | 33 | (75.0) | 15 | (45.5) | |
IV | 5 | (11.4) | 8 | (24.2) | |
Histological types (%) | 0.24 | ||||
Serous carcinoma | 26 | (59.1) | 18 | (54.6) | |
Clear cell carcinoma | 5 | (11.4) | 9 | (27.3) | |
Endometrioid carcinoma | 6 | (13.6) | 1 | (3.0) | |
Carcinosarcoma | 1 | (2.3) | 1 | (3.0) | |
Squamous cell carcinoma | 1 | (2.3) | 0 | (0) | |
Mucinous carcinoma | 0 | (0) | 1 | (3.0) | |
Adenocarcinoma not otherwise specified | 5 | (11.4) | 3 | (9.1) | |
Residual tumor (≥ 1 cm) at primary surgery (%) | 0.08 | ||||
Yes | 22 | (50.0) | 10 | (30.3) | |
No | 22 | (50.0) | 23 | (69.7) | |
Prior chemotherapy regimens before bevacizumab-containing regimens (times) | 3.8 | (1–11) | 3.5 | (1–11) | 0.61 |
Total dose of bevacizumab set for the first time during the first cycle (mg) | 400.0 | (400) | 745.6 | (520–1113) | < 0.01 |
Best response | 0.13 | ||||
Complete remission | 3 | (6.8) | 0 | (0) | |
Partial remission | 6 | (13.6) | 6 | (18.2) | |
Stable disease | 27 | (61.4) | 15 | (45.5) | |
Progressive disease | 8 | (18.2) | 12 | (36.4) | |
Response rate (%) | 20 | 18.2 | 0.52 | ||
Clinical benefit rate (%) | 82 | 63.6 | 0.07 | ||
Stable duration (months) | 8 | (0–37) | 5 | (0–10) | < 0.01 |