Skip to main content
. 2018 Jul 8;17:1533033818785496. doi: 10.1177/1533033818785496

Table 4.

Percentage of Evaluated Patients Without ADT, GI and GU Adverse Effects, PSA Concentration, and Pain Intensity of Evaluated Patients During FU.

Time After SABR SABR End 1 Month 3 Months 6 Months 9 Months 12 Months 15 Months 18 Months 21 Months 24 Months 30 Months 36 Months 42 Months 48 Months
n (%) 38 (100) 23 (61) 29 (76) 27 (71) 24 (63) 24 (63) 13 (34) 9 (24) 9 (24) 9 (24) 7 (18) 9 (24) 9 (24) 5 (13)
Without ADT (%) 44.7 43.5 48.3 47.8 50 (5% CT) 47.6 (9.5% CT) 30.8 55.6 55.6 33.3 28.6 55.6 33.3 20
GI 0 (%) 97.4 95.5 92.6 95.7 90.4 85.7 92.3 100 100 100 100 88.9 100 100
GI 1 (%) 2.6 4.5 7.4 4.3 4.8 9.5 7.7 11.1
GI 2 (%) 4.8 4.8
GI 3 (%)
GU 0 (%) 78.9 59.1 70.4 69.6 81.0 71.4 75.0 88.9 77.8 87.5 85.7 88.9 77.8 80
GU 1 (%) 15.8 31.8 18.5 17.4 4.8 20.8 8.3 11.1 14.3 11.1 22.2 20
GU 2 (%) 5.3 9.1 7.4 13.0 9.4 4.8 16.7 11.1
GU 3 (%) 3.7 4.8 11.1 12.5
PSA mean 5.98 2.14 2.76 3.70 2.32 12.20 21.90 176.83 14.20 4.42 21.06 20.22 35.97 130.45
PSA median 3.26 0.87 0.65 0.27 0.24 0.42 1.11 1.20 1.50 0.84 0.84 1.09 2.19 0.80
BPI mean 0.026 0.182 0.259 0.044 0.667 0.250 0.000 0.111 0.000 0.500 0.000 0.000 0.556 1.25

Abbreviations: ADT, androgen deprivation therapy; BPI, Brief Pain Inventory; CT, chemotherapy; FU, follow-up; GI, gastrointestinal; GU, genitourinary; PSA, prostate-specific antigen; SABR, stereotactic ablative radiotherapy.