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Table 2 Backgrounds of the patients for analysis

From: Objective evaluation of chemotherapy-induced peripheral neuropathy using quantitative pain measurement system (Pain Vision®), a pilot study

   All patient (n = 41) With CIPN (n = 28) Without CIPN (n = 13)
Age   55.8 ± 11.0 57.0 ± 10.7 53.2 ± 11.6
Cancer type Ovarian 22 16 6
Cervical 11 5 6
Endometrial 8 7 1
Regimen TC ± BV 34 27 7
TP 5 1 4
PTX + NED 2 0 2
Cycle   5.9 ± 0.4 5.9 ± 0.3 5.7 ± 0.7
Body-surface area (m2)   1.484 ± 0.126 1.472 ± 0.121 1.509 ± 0.137
Cumulative PTX dose (mg/m2)   1000.6 ± 101.3 1028.5 ± 38.6 940.8 ± 158.6
Cumulative Platinum dose (mg/m2) CBDCA 2328.9 ± 305.5 2340.7 ± 294.5 2283.6 ± 366.7
CDDP 514.8 ± 112.4 296 331.8 ± 35.1
NED 604.0 ± 5.7 - 400
  1. Values are indicated as means ±standard deviations
  2. PTX paclitaxel, CBDCA carboplatin, CDDP cisplatin, NED nedaplatin, TC ± BV bevacizumab (15 mg/kg) ± paclitaxel (175 mg/m2) + carboplatin (AUC = 6), TP paclitaxel (175 mg/m2) + cisplatin (75 mg/m2), PTX-NED paclitaxel (175 mg/m2) + nedaplatin (80 mg/m2)