Clinical Study

Efficacy of Immediate Switching from Bicalutamide to Flutamide as Second-Line Combined Androgen Blockade

Table 2

The clinical factors in the responders and nonresponders to second-line CAB therapy.

Responders (50% PSA change)Nonresponders value

Number of patients (%)8 (40%)12 (60%)
Clinical stage, (%)
 T21 (12.5)0 (0)
 T35 (62.5)6 (50)
 T42 (25.0)6 (50)0.25
Gleason score, (%)
 61 (12.5)0 (0.0)
 71 (12.5)2 (16.7)
 82 (25.0)2 (16.7)
 94 (50.0)7 (58.4)
 100 (0)1 (8.3)0.654
Mean PSA at the diagnosis, ng/mL (range)487.5 (23.8–2350)941 (17.2–5740)0.94
Mean nadir PSA after first-line CAB therapy, ng/mL (range)2.06 (0.003–14.7)2.67 (0.011–16.8)0.11
Mean duration to nadir PSA after first-line CAB, months12.3 (3–26)13.8 (2–48)0.64
Mean duration of first-line CAB therapy, months23 (11–38)18.4 (7–50)0.32
Mean PSA at the start of second-line CAB therapy, ng/mL (range)4.88 (0.116–20.7)24.8 (0.114–116.3)0.09
Mean duration of the response to second-line CAB therapy, months18.4 (3–26)
AWS01

CAB: combined androgen blockade; AWS: antiandrogen withdrawal syndrome.