Characteristic | No. patients | Percentage | |
---|---|---|---|
Total | 259 | 100 | |
Sex | |||
Male | 194 | 74.9 | |
Female | 65 | 25.1 | |
Median age (range); years | 49 (19–74) | ||
T category | |||
T 1–2 | 34 | 13.1 | |
T 3–4 | 225 | 86.9 | |
N category | |||
N 0–1 | 89 | 34.4 | |
N 2–3 | 170 | 65.6 | |
Stage | |||
III | 129 | 49.8 | |
IVA | 130 | 50.2 | |
Plasma EBV-DNA (copies/mL) | |||
≤ 500 | 173 | 66.8 | |
> 500 | 86 | 33.2 | |
95% of target volume received dose greater than (D95, Gy) | |||
Average dose of nasopharynx (PTVnx + rn) (range) | 70.2 (66.1–74.3) | ||
Average dose of neck node (PTVnd) (range) | 69.4 (60.7–75.9) | ||
Sites of residual | |||
Primary focus | 121 | 46.7 | |
Retropharyngeal lymph nodes | 54 | 20.8 | |
Cervical lymph nodes | 152 | 58.7 | |
Median time to boost after RT (range); days | 36 (1–74) | ||
Average boost dose for primary focus (range); Gy | 8.1 (4–12.5) | ||
Average boost dose for retropharyngeal lymph nodes (range); Gy | 8.3 (5–12.5) | ||
Average boost dose for cervical lymph nodes (range); Gy | 8.6 (4–18) |