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. 2016 Jul 25;89(1065):20150981. doi: 10.1259/bjr.20150981

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.

a

Log-rank test for univariate analysis.

b

Wald test from Cox regression multivariate model.

c

Includes NCCN risk group, V100, D90, neoadjuvant AD therapy, radioactive isotope, age and prostatic volume at implantation.

d

Includes the same variables of c plus the interaction term.