Table 2. Patient and Treatment Characteristics.
Characteristic | Value (N = 2142) |
---|---|
Age | |
Mean (SD), y | 67.9 (9.5) |
Median (range), y | 68 (41-92) |
Risk grouping, No. (%) | |
Low risk | 1185 (55.3) |
Favorable intermediate risk | 692 (32.3) |
Unfavorable intermediate riska | 265 (12.4) |
Gleason grade, No. (%) | |
I | 1355 (63.3) |
II | 614 (28.7) |
III | 173 (8.1) |
Clinical T stage, No. (%) | |
T1c | 1595 (74.5) |
T2a | 430 (20.1) |
T2b | 104 (4.9) |
T2c | 13 (0.6) |
Initial prostate-specific antigen level | |
Mean (SD), ng/mL | 6.4 (3.1) |
Median (range), ng/mL | 5.7 (0.09-19.9) |
Equivalent dose in 2-Gy fractions, No. (%) | |
≥91 Gy | 797 (37.2) |
<91 Gy | 1346 (62.8) |
Treatment platform, No. (%) | |
Robotic arm–mounted linear acceleratorb | 1479 (69.0) |
Gantry-mounted linear accelerator | 664 (31.0) |
Fractionation, No. (%) | |
Daily | 1013 (47.3) |
Every other day | 1015 (47.4) |
Weekly | 114 (5.3) |
Androgen deprivation therapy use, No./total No. (%) | |
Total | 115/2142 (5.4) |
Low | 43/1185 (3.6) |
Favorable | 47/692 (6.8) |
Unfavorable | 25/265 (9.4) |
Duration of androgen deprivation therapy, mean (SD), mo | 3.6 (4.2) |
Percentage of positive cores was not available for 248 of 957 intermediate-risk patients (25.9%) who did not have other factors that could classify them as having unfavorable intermediate-risk disease; in instances of ambiguity, patients were classified conservatively as having favorable intermediate-risk disease.
CyberKnife (Accuray Inc).