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. 2024 Aug 16;49:100843. doi: 10.1016/j.ctro.2024.100843

Table 1.

Baseline patient and treatment characteristics.

Variables CFRT (n = 90) MHRT (n = 90) UHRT (n = 60) p-value
Age (median, IQR) 77 (71–80) 75 (70–79) 74 (68–79) 0.1
Risk group (n, %)
UIR
High risk

0
90 (100 %)

0
90 (100 %)

13 (21.7 %)
47 (78.3 %)
<0.0001
Grade group (n, %)
1
2
3
4
5
Unknown

0
14 (15.6 %)
10 (11.1 %)
33 (36.7 %)
29 (32.2 %)
4 (4.4 %)

1 (1.1 %)
5 (5.6 %)
8 (8.9 %)
39 (43.3 %)
32 (35.6 %)
5 (5.6 %)

1 (1.7 %)
10 (16.7 %)
15 (25 %)
18 (30 %)
16 (26.7 %)
0 (0 %)
0.03
Clinical stage (n, %)
T1c
T2a
T2b
T2c
T3a
T3b
Unknown

28 (31.1 %)
27 (30 %)
14 (15.6 %)
8 (8.9 %)
8 (8.9 %)
1 (1.1 %)
4 (4.4 %)

30 (33.3 %)
23 (25.6 %)
12 (13.3 %)
7 (7.8 %)
12 (13.3 %)
1 (1.1 %)
5 (5.6 %)

10 (16.7 %)
17 (28.3 %)
10 (16.7 %)
11 (18.3 %)
8 (13.3 %)
3 (5 %)
1 (1.7 %)
0.3
Baseline PSA (median, IQR) 15.7 (7.1–26.5) 13.5 (7.5–23.6) 11.8 (6.9–19.9) 0.3
Baseline PSA categories (n, %)
<10
10–20
>20
Unknown

31 (34.4 %)
21 (23.3 %)
35 (38.9 %)
3 (3.3 %)

30 (33.3 %)
27 (30 %)
29 (32.2 %)
4 (4.4 %)

22 (36.7 %)
23 (38.3 %)
15 (25 %)
0 (0 %)
0.3
Risk of lymph node involvement (median, IQR) 33.1 (10.4–73.7) 32.9 (17.9–80.0) 26.9 (21.7–33.0) 0.0006
Duration of ADT (median, IQR) 22.2 (15–29.5) 22 (15–30.1) 12 (6.2–15.9) <0.0001
Duration of ADT categories (n, %)
0 months
≤12 months
>12–24 months
≥24 months

5 (5.6 %)
17 (18.9 %)
29 (32.2 %)
39 (43.3 %)

3 (3.3 %)
15 (16.7 %)
35 (38.9 %)
37 (41.1 %)

4 (6.6 %)
24 (40 %)
31 (51.7 %)
1 (1.7 %)
<0.0001

*CFRT: conventionally fractionated radiotherapy; MHRT: moderately hypofractionated radiotherapy; UHRT: ultrahypofractionated radiotherapy; IQR: interquartile range; UIR: unfavorable intermediate risk; PSA: prostate specific antigen; ADT: androgen deprivation therapy.