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Table 4 PSA response rate, overall survival, and time-to-treatment failure

From: Real-world efficacy and safety of two doses of cabazitaxel (20 or 25 mg/m2) in patients with castration-resistant prostate cancer: results of a Japanese post-marketing surveillance study

Outcome

C20

C25

Statistic

N

Response rate, n (%)

N

Response rate, n (%)

OR (95% CI)

p

PSA response

601

169 (28.1)b

    

 Unadjusted

177

49 (27.7)

146

46 (31.5)

1.20 (0.74–1.94)

0.453

 Multivariablea

135

38 (28.2)

120

36 (30.0)

1.18 (0.66–2.13)

0.572

 PSM

106

28 (26.4)

103

33 (32.0)

1.31 (0.72–2.39)

0.372

Outcome

N

Median (95% CI)

N

Median (95% CI)

HR (95% CI)

p

OS (days)

656

319 (293–361)b

    

 Unadjusted

188

287 (240–326)

159

NR

0.71 (0.53–0.97)

0.030

 Multivariablea

141

287 (234–327)

129

NR

0.69 (0.48–0.99)

0.047

 PSM

110

291 (230–NR)

112

NR

0.73 (0.50–1.08)

0.119

TTF (days)

660

116 (108–135)b

    

 Unadjusted

190

113 (94–137)

159

120 (104–157)

0.78 (0.62–0.97)

0.026

 Multivariablea

143

115 (92–138)

129

115 (99–157)

0.71 (0.54–0.93)

0.014

 PSM

112

122 (90–148)

112

120 (109–158)

0.75 (0.57–0.99)

0.046

  1. C20 20 mg/m2 cabazitaxel, C25 25 mg/m2 cabazitaxel, PSA Prostate-specific antigen, OR Odds ratio, CI Confidence interval, PSM Propensity score matching, HR Hazard ratio, OS Overall survival, NR Not reached, TTF Time-to-treatment failure
  2. aCovariates were: age, body surface area, duration of disease, Gleason score, TNM, performance status, PSA, medical history, complications, curative intent focal therapy, palliative radiation therapy, and previous treatment (docetaxel, enzalutamide or abiraterone acetate)
  3. bIn all available patients