Table 5.
Biochemical failure-free survival (BFFS) in subgroups
| Subgroups | Total | Events | Univariate analysis |
Multivariate analysisc |
||||
|---|---|---|---|---|---|---|---|---|
| 3-year BFFS (%) | 5-year BFFS (%) | 7-year BFFS (%) | p-valuea | RR (95% CI) | p-valueb | |||
| All patientsb | 2237 | 207 | 95.7 | 91.9 | 88.5 | |||
| NCCN risk group classification | ||||||||
| Low risk | 1485 | 93 | 97.0 | 94.8 | 92.8 | <0.001 | 1 | |
| Intermediate risk | 582 | 91 | 93.8 | 86.0 | 78.4 | 2.60 (1.93–3.51) | <0.0001 | |
| High risk | 41 | 10 | 78.9 | 73.0 | 73.0 | 3.02 (1.38–6.60) | 0.006 | |
|
V100 (%) | ||||||||
| <90% | 642 | 77 | 95.3 | 90.1 | 86.4 | 0.03 | 1 | |
| ≥90% | 1582 | 128 | 96.0 | 92.8 | 89.5 | 0.76 (0.55–1.04) | 0.09 | |
|
D90 (% of the prescribed dose) | ||||||||
| <90% | 668 | 62 | 95.8 | 91.1 | 89.1 | 0.49 | 1 | |
| ≥90% | 1555 | 143 | 95.8 | 92.3 | 88.5 | 1.01 (0.72–1.42) | 0.93 | |
| Neoadjuvant AD therapy | ||||||||
| No | 1099 | 96 | 96.3 | 92.6 | 89.2 | 0.59 | 1 | |
| Yes | 882 | 80 | 95.8 | 92.0 | 89.1 | 0.79 (0.58–1.07) | 0.13 | |
| Radioactive isotope | ||||||||
| 125I | 2185 | 202 | 95.7 | 91.9 | 85.5 | 0.45 | 1 | |
| 103Pd | 52 | 5 | 96.1 | 91.7 | 89.1 | 0.92 (0.37–2.25) | 0.85 | |
| Age (years) | ||||||||
| <55 | 102 | 7 | 96.9 | 95.7 | 90.9 | 0.42 | 1 | |
| 55–64 | 637 | 56 | 94.6 | 93.4 | 90.8 | 1.31 (0.59–2.88) | 0.51 | |
| 65–74 | 1187 | 112 | 96.3 | 91.5 | 88.0 | 1.38 (0.64–2.97) | 0.42 | |
| ≥75 | 311 | 32 | 95.2 | 88.7 | 84.7 | 1.50 (0.65–3.46) | 0.34 | |
| Interactionsd | ||||||||
| NCCN risk group–V100 | ||||||||
| ≥90% vs <90% (low-risk group) | 0.53 (0.33–0.84) | 0.04 | ||||||
| ≥90% vs <90% (intermediate-/high-risk group) | 1.09 (0.69–1.74) | |||||||
| NCCN risk group–neoadjuvant AD therapy | ||||||||
| AD therapy vs no AD therapy (low-risk group) | 0.56 (0.35–0.89) | 0.07 | ||||||
| AD therapy vs no AD therapy (intermediate-/high-risk group) | 1.09 (0.69–1.71) | |||||||
| NCCN risk group–radioactive isotope | ||||||||
| 103Pd vs125I (low-risk group) | 0.43 (0.10–1.76) | 0.10 | ||||||
| 103Pd vs125I (intermediate-/high-risk group) | 2.34 (0.72–7.61) | |||||||
125I, iodine-125; 103Pd, palladium-103; AD, androgen deprivation; CI, confidence interval; D90, dose received by 90% of target volume; NCCN, National Comprehensive Cancer Network; RR, relative risk; V100; target volume receiving 100% of prescribed dose.
The sum of the number of patients among levels of a variable could be not equal to the total number of patients (N = 2237).
The “not available (N/A)” subgroups, although included both in univariate and multivariate models, have not been shown in this table.
Log-rank test for univariate analysis.
Wald test from Cox regression multivariate model.
Includes NCCN risk group, V100, D90, neoadjuvant AD therapy, radioactive isotope, age and prostatic volume at implantation.
Includes the same variables of c plus the interaction term.