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. 2018 Nov 20;51(3):1144–1155. doi: 10.4143/crt.2018.508

Table 1.

Patients’ clinicopathologic characteristics

Characteristic Value (n=866)
Age (yr) 53.5±11.2
BMI (kg/m2) 23.4±3.4
Co-morbidities
 Hypertension
  No 698 (80.6)
  Yes 168 (19.4)
 Diabetes
  No 797 (92.0)
  Yes 69 (8.0)
 Dyslipidemia
  No 803 (92.7)
  Yes 61 (7.0)
  Unknown 2 (0.2)
Pretreatment CBC
 Hemoglobin (g/dL) 12.3±1.3
 Platelets (×103/μL) 327.5±104.2
 WBC (×103/μL) 7.1±2.5
  Segmented neutrophils (%) 66.3±10.1
   Count (×10/μL) 478.4±215.3
  Lymphocytes (%) 24.3±9.0
   Count (×10/μL) 160.2±56.2
  Monocytes (%) 6.9±2.3
   Count (×10/μL) 47.5±23.4
ln(CA-125) (IU/mL) 5.8±1.9
FIGO stage
 I 220 (25.4)
 II 62 (7.2)
 III 441 (50.9)
 IV 143 (16.5)
Histologic type
 Serous 529 (61.1)
 Endometrioid 96 (11.1)
 Mucinous 79 (9.1)
 Clear cell 85 (9.8)
 Others 77 (8.9)
Primary treatment strategy
 PDS 712 (82.2)
 NAC 154 (17.8)
Residual tumor after PDS/IDS (cm)
 No gross 638 (73.7)
 < 1 144 (16.6)
 1-2 44 (5.1)
 > 2 31 (3.6)
 Unknown 9 (1.0)
Post-operative taxane- and platinum-based chemotherapy
 No 74 (8.5)
 Yes 792 (91.5)
  CRa) 616 (71.1)
  PR 108 (12.5)
  SD 13 (1.5)
  PD 55 (6.4)
Recurrence
 No 425 (49.1)
 Yes 441 (50.9)
  No post-operative chemotherapy 8 (0.9)
  PSRb) 285 (32.9)
  PRR 148 (17.1)
Platinum sensitivity
 Platinum-sensitivec) 562 (64.9)
 Platinum-resistant 148 (17.1)

Values are presented as mean±standard deviation or number (%). BMI, body mass index; CA-125, cancer antigen 125; CBC, complete blood count; WBC, white blood cell; FIGO, International Federation of Gynecology and Obstetrics; PDS, primary debulking surgery; NAC, neoadjuvant chemotherapy; IDS, interval debulking surgery; CR, complete remission; PR, partial remission; SD, stable disease; PD, progressive disease; PSR, platinum-sensitive recurrence; PRR, platinum-resistant recurrence; SD, standard deviation.

a)

Reponses to chemotherapy were evaluated by Response Evaluation Criteria in Solid Tumors (RECIST) ver. 1.1,

b)

PSR was defined as relapse ≥ 6 months after completion of taxane- and platinum-based chemotherapy, whereas PRR as relapse < 6 months,

c)

In addition to PSR, the patients who completed taxane- and platinum-based chemotherapy and did not experience disease recurrence during at least 6 months of follow-up period were considered platinum-sensitive.