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. 2006 Aug 1;95(5):627–633. doi: 10.1038/sj.bjc.6603300

Table 1. Clinicopathological characteristics and results of p53 immunostaining.

  UK patients (n=288) Dutch patients (n=188) All patients (n=476)
Age (years)
 Median 58 59 59
 Range 23–87 22–83 22–87
       
PFS (months)
 Median 13 18 15
 Range 0–135 0–158 0–158
       
OS (months)
 Median 30 33 31
 Range 0–136 37–186 0–186
       
FIGO stage
 Stage I 21 (7.3%) 23 (12.1%) 44 (9.2%)
 Stage II 39 (13.5%) 18 (9.6%) 57 (12.0%)
 Stage III 181 (62.8%) 117 (62.2%) 298 (62.6%)
 Stage IV 47 (16.3%) 29 (15.4%) 76 (16.0%)
 Missing 0 1 (0.5%) 1 (0.2%)
       
Tumour type
 Serous 154 (53.5%) 105 (55.9%) 259 (54.4%)
 Mucinous 14 (4.9%) 15 (8.0%) 29 (6.1%)
 Clear cell 15 (5.2%) 13 (6.9%) 28 (5.9%)
 Endometrioid 36 (12.5%) 26 (13.8%) 62 (13.0%)
 Adenocarcinoma 37 (12.8%) 20 (10.6%) 57 (12.0%)
 Other 30 (10.4%) 9 (4.8%) 39 (8.2%)
 Missing 2 (0.7%) 0 2 (0.4%)
       
Tumour grade
 Grade I 19 (6.6%) 23 (12.2%) 47 (9.9%)
 Grade II 73 (25.3%) 42 (22.3%) 120 (25.2%)
 Grade III 158 (54.9%) 96 (51.1%) 256 (53.8%)
 Missing 38 (13.2%) 27 (14.4%) 53 (11.1%)
       
Residual disease
 <2 cm 140 (48.6%) 65 (34.6%) 207 (43.5%)
 ⩾2 cm 142 (49.3%) 110 (58.5%) 250 (52.5%)
 Missing 6 (2.1%) 13 (6.9%) 19 (4.0%)
       
Type of chemotherapy
 Platinum containing 98 (34.0%) 95 (50.5%) 195 (41.0%)
 Platinum and taxane containing 165 (57.3%) 72 (38.3%) 237 (49.8%)
 Other regimen 25 (8.7%) 21 (11.2%) 44 (9.2%)
       
P53 expression
 Normal 133 (46.2%) 99 (52.7%) 228 (47.9%)
 Aberrant 155 (53.8%) 89 (47.3%) 248 (52.1%)

FIGO=International Federation of Gynaecology and Obstetrics; OS=overall survival; PFS=progression-free survival.