Table 2. Correlation of EDD expression with clinicopathological and gene expression variablesa.
| Variable | P-valueb |
|---|---|
| Age | 0.20 |
| FIGO Stage | 0.12 |
| Tumour grade | 0.17 |
| Surgical debulking | 0.59 |
| Menopausal status | 0.52 |
| CA125 | 0.027 |
| Adjuvant chemotherapy | |
| P only | 0.94 |
| P+C | 0.44 |
| P+T | 0.38 |
| M only | 0.97 |
| VEGF >2 vs ⩽2 | 0.80 |
| p53 >10% vs ⩽10% | 0.50 |
| p27Kip1 ⩽65% vs >65% | 0.22 |
| p21Wap/Cif1 ⩽10% vs >10% | 0.22 |
| Cyclin D1 >10% vs ⩽10% | 0.90 |
| Cyclin E >10% vs ⩽10% | 0.21 |
C=cyclophosphamide; M=melphalan; P=platinum; T=paclitaxel.
EDD expression was modelled as a continuous variable. Clinicopathological and gene expression variables were dichotomised as shown in Table 1, as described in the text (VEGF) and Bali et al, 2004 (cell cycle markers).
Bold type indicates significant P-values.