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, (%) | | | | T2 | 1 (12.5) | 0 (0) | | T3 | 5 (62.5) | 6 (50) | | T4 | 2 (25.0) | 6 (50) | 0.25 | Gleason score, (%) | | | | 6 | 1 (12.5) | 0 (0.0) | | 7 | 1 (12.5) | 2 (16.7) | | 8 | 2 (25.0) | 2 (16.7) | | 9 | 4 (50.0) | 7 (58.4) | | 10 | 0 (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, months | 12.3 (3–26) | 13.8 (2–48) | 0.64 | Mean duration of first-line CAB therapy, months | 23 (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, months | 18.4 (3–26) | — | — | AWS | 0 | 1 | — |
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CAB: combined androgen blockade; AWS: antiandrogen withdrawal syndrome.
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