Skip to main content
. Author manuscript; available in PMC: 2014 Sep 12.
Published in final edited form as: Gynecol Oncol. 2009 Oct 17;116(1):61–65. doi: 10.1016/j.ygyno.2009.09.018

Table 2.

Patient demographics

Cases PFS OS
Subjects n=253
Age 61.8 ± 11.4 0.002 0.001

Type of cancer
 Ovarian cancer 224 (88.5%) 0.45 0.42
 Primary peritoneal cancer 24 (9.5%)
 Fallopian cancer 5 (2.0%)

Lymph nodes metastasis 99 (39.1%) 0.54 0.57
Lympho-vascular invasion 92 (36.4%) 0.006 0.001

FIGO Stage 0.09 0.08
 IIIA and IIIB 7 (2.8%)
 IIIC 211 (83.4%)
 IV 35 (13.8%)

Histologic type 0.4 0.46
 Serous 206 (81.4%)
 Endometrioid 9 (3.6%)
 Mucinous 5 (2.0%)
 Undifferentiated 5 (2.0%)
 Clear cell 5 (2.0%)
 Mixed 21 (8.3%)
 Other 2 (0.8%)

Tumor size 8.5 cm (1.2–24.5) 0.11 0.33
High grade tumor 194 (76.7%) 0.72 0.12
Preoperative CA-125 677 IU/L (8–5620) 0.006 0.03

Optimal surgery 105 (41.5%) <0.001 <0.001
Bowel resection 88 (34.8%) 0.023 0.017

Type of chemotherapy
 Carboplatin + Paclitaxel 119 (52.4%) 0.002 <0.001
 Carboplatin + Docetaxel 72 (31.7%)
 Cisplatin + Paclitaxel 34 (15.0%)
 Carboplatin + Cyclophosphamide 2 (0.9%)
 Number of cycles 6 (0–12) <0.001 <0.001
 Chemotherapy response* 184 (81.0%) <0.001 <0.001

Site of recurrence 196 (77.4%)
 Extrapelvis 116 (68.2%)
 Pelvis 31 (18.2%)
 Chest 14 (8.2%)
 Other 9 (5.3%)

Univariate analysis was performed between each variable and survival outcomes (PFS or OS) (P-value is shown). Comparisons of variables were performed for: ovarian vs primary peritoneal vs fallopian cancer for type of cancer; Stage III vs IV for FIGO Stage; serous vs non-serous for histology; and carboplatin + paclitaxel vs carboplatin + docetaxel vs cisplatin + paclitaxel vs carboplatin + cyclophosphamide. Crude tumor size and preoperative CA-125 were compared to survival.

*

227 cases with available response.

17 cases, no chemotherapy.

Abbreviations: PFS, progression-free survival; and OS, overall survival.