Table 3. PFS and PSA response rate performance of the risk model in this study.
Risk group | No. (%) | PSA response rate (%) | Median PFS (months) | HR (95% CI) | P value |
---|---|---|---|---|---|
Low risk | 65 (40.6) | 42/65 (64.6) | 3.6 | 1.619 (1.444–1.815) | Reference |
Moderate risk | 38 (23.8) | 9/38 (23.7) | 3.0 | <0.001 | |
High risk | 57 (35.6) | 0/57 (0) | 1.4 |
Abbreviations: CI, confidence interval; HR, hazard rate; PFS, progression-free survival; PSA, prostate-specific antigen; PSADT, PSA doubling time.
Low risk denotes patients with 0–1 risk factor, moderate risk denotes 2 risk factors and high risk denotes 3–4 risk factors. The risk factors included a nadir PSA of ≥0.2 ng ml−1, a baseline testosterone of <0.1 ng ml−1, a baseline haemoglobin less than normal (<120 g l−1) and a PSADT of <2 months. The PSA response rate was defined as the percentage of patients with a PSA decline of ≥50% compared with the baseline PSA level during the ketoconazole therapy.