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Table 3 Univariate and multivariate analyses for progression-free survival after bevacizumab administration in all cases included in this study

From: Potential efficacy of weekly low-dose administration of bevacizumab as a combination therapy for platinum-resistant ovarian carcinoma: a retrospective analysis

  

Univariate analysis

Multivariate analysis

Variables

 

Hazard ratio (95% CI)

p-Value

Hazard ratio (95% CI)

p-Value

Method of bevacizumab administration

Group A vs. group B

0.47 (0.27–0.80)

 < 0.01

0.53 (0.29–0.95)

0.03

Age (years)

 ≥ 50 vs. < 50

1.83 (1.01–3.50)

0.045

1.40 (0.73–2.81)

0.31

Drug combined with bevacizumab

Gemcitabine vs. other regimens

1.70 (0.95–3.25)

0.08

  

Histology

Serous carcinoma vs. other histology

0.73 (0.43–1.24)

0.24

  

Residual tumor at primary surgery

 < 1 cm vs. ≥ 1 cm

0.94 (0.55–1.58)

0.82

  

FIGO stage

I, II vs. III, IV

0.98 (0.54–1.90)

0.95

  
  1. Group A was defined as patients treated with weekly low-dose administration of bevacizumab
  2. Group B was defined as patients treated with monthly high-dose administration of bevacizumab
  3. CI confidence interval, FIGO International Federation of Gynecology and Obstetrics