Center for Proton Therapy, Paul Scherrer Institute, ETH Domain, CH-5232, Villigen, Switzerland.
Service d'Epidemiologie Clinique, Hôpitaux Universitaire de Genève, CH 12011 Geneva, Geneva, Switzerland.
Br J Radiol. 2020 Mar;93(1107):20190028. doi: 10.1259/bjr.20190028. Epub 2019 Aug 1.
To assess the radiation-induced optic neuropathy (RION) prevalence, following high dose pencil beam scanning proton therapy (PBSPT) to skull base and head and neck (H&N) tumours.
Between 1999 and 2014, 216 adult patients, median age 47 years (range, 18-77), were treated with PBS PT for skull base or H&N malignancies, delivering ≥45 Gy to the optic nerve(s) (ON) and/or optic chiasma (OC). The median administered dose to the planning target volume was 74.0 Gy (range, 54.0-77.4). The median follow-up was 5.3 years (range, 0.8-15.9).
RION was observed in 14 (6.5%) patients at a median time of 13.2 months (range, 4.8-42.6) following PBSPT. Most (92.9%) of RION were symptomatic. Most affected patients (11/14; 79%) developed unilateral toxicity. Grade 4, 3, 2 and 1 toxicity was observed in 10, 2, 1 and 1 patients, respectively. On univariate analyses, age (<70 ≥70 years; < 0.0001), hypertension ( = 0.0007) and tumour abutting the optic apparatus ( = 0.012) were associated with RION. OC's V60 Gy was of border line significance ( = 0.06). None of the other evaluated OC-ON dose/volume metrics (Dmax, Dmean, V40-60) were significantly associated with this complication.
These data suggest that high-dose PBS PT for skull base and H&N tumours is associated with a low prevalence of RION. Caution should be however exercised when treating elderly/hypertensive patients with tumours abutting the optic apparatus.
This is the first study reporting the risk of developing RION following proton therapy with PBS technique, demonstrating the safety of this treatment.
评估高剂量笔形束扫描质子治疗(PBSPT)颅底和头颈部(H&N)肿瘤后放射性视神经病变(RION)的发生率。
1999 年至 2014 年间,216 例成年患者,中位年龄 47 岁(范围 18-77 岁),因颅底或 H&N 恶性肿瘤接受 PBSPT 治疗,视神经(ON)和/或视交叉(OC)接受≥45Gy 剂量照射。计划靶区接受的中位照射剂量为 74.0Gy(范围 54.0-77.4Gy)。中位随访时间为 5.3 年(范围 0.8-15.9 年)。
在接受 PBSPT 后中位时间 13.2 个月(范围 4.8-42.6)时,14 例(6.5%)患者出现 RION。大多数(92.9%)RION 为症状性。受影响的大多数患者(14 例中的 11 例;79%)发生单侧毒性。4 级、3 级、2 级和 1 级毒性分别在 10 例、2 例、1 例和 1 例患者中观察到。单因素分析显示,年龄(<70 岁≥70 岁;<0.0001)、高血压(=0.0007)和肿瘤毗邻视神经(=0.012)与 RION 相关。OC 的 V60Gy 具有边界显著性(=0.06)。其他评估的 OC-ON 剂量/体积指标(Dmax、Dmean、V40-60)均与该并发症无显著相关性。
这些数据表明,颅底和 H&N 肿瘤的高剂量 PBSPT 与 RION 的低发生率相关。然而,在治疗毗邻视神经的肿瘤的老年/高血压患者时应谨慎。
这是第一项报道使用 PBS 技术质子治疗后发生 RION 风险的研究,证明了这种治疗的安全性。