van Werkhoven Lucy A, Mattioli Chiara, Milder Maaike T W, Loi Mauro, Nuyttens Joost J
Department of Radiotherapy, Erasmus MC Cancer Institute, University Medical Center Rotterdam, The Netherlands.
Radiation Oncology, Azienda Ospedaliero Universitaria Careggi, Università di Firenze, Firenze, Italy.
Int J Radiat Oncol Biol Phys. 2025 Jun 18. doi: 10.1016/j.ijrobp.2025.05.087.
This study evaluated late ureteral toxicity in relation to dose in patients treated with stereotactic body radiation therapy (SBRT) on abdominopelvic lymph node (A-P LN) oligometastases and assessed differences between planned and received ureteral dose.
Patients treated between 2011 and 2023 with SBRT on A-P LN oligometastases from various primary tumors were retrospectively reviewed. Toxicity was graded using the Common Terminology Criteria for Adverse Events version 5.0. Dose-volume histogram parameters (maximum dose to the ureter [D] maximum dose to 0.1 cc of the ureter [D], and maximum dose to 0.5 cc of the ureter [D]) from ureters receiving >10 Gy were extracted and compared with published ureteral constraints (D 108, D 108, and D 77 Gy equivalent dose of 2 Gy per fraction with a:b ratio of 3 Gy [EQD2]). Interfraction dose variation was derived from patients who were treated with online adaptive SBRT.
The study included 144 patients, of whom 121 had a total of 137 ureters that were treated with <10 Gy. Most patients (85%) received 45 Gy in 5 fractions. The median ureter D and D were 60 and 42 Gy EQD2, respectively. No grade (G) ≥ 4 toxicities were observed. Three patients (2%) developed G3 ureteral obstruction, with D values of 121, 97, and 74 Gy EQD2. Five patients (4%) experienced any G of late urinary toxicity, but only 1 of them exceeded the D of 108 Gy EQD2. In total, 31 (23%) patients did not experience late toxicity, despite exceeding this parameter. No significant difference was found between the planned and received ureter dose (D 25 vs 22 Gy EQD2P = .23). The median follow-up was 28 months.
The incidence of G3 ureteral toxicity after SBRT on A-P LN oligometastases is low (2%). Published dose constraints were violated in 23% of the patients without reported toxicity, suggesting other factors may contribute. Furthermore, no difference was found between the planned and received ureter dose, indicating that the planned dose is a reliable estimate of the dose received.
本研究评估了立体定向体部放射治疗(SBRT)用于治疗腹盆腔淋巴结(A-P LN)寡转移患者时输尿管晚期毒性与剂量的关系,并评估了计划输尿管剂量与实际接受的输尿管剂量之间的差异。
回顾性分析2011年至2023年间接受SBRT治疗各种原发性肿瘤所致A-P LN寡转移的患者。使用不良事件通用术语标准第5.0版对毒性进行分级。提取接受超过10 Gy照射的输尿管的剂量体积直方图参数(输尿管最大剂量[D]、输尿管0.1 cc的最大剂量[D]和输尿管0.5 cc的最大剂量[D]),并与已发表的输尿管限制剂量(D 108、D 108和D 77 Gy,等效剂量为每分次2 Gy,a:b比值为3 Gy[EQD2])进行比较。分次间剂量变化来自接受在线自适应SBRT治疗的患者。
该研究纳入144例患者,其中121例患者的137条输尿管接受的照射剂量<10 Gy。大多数患者(85%)接受5次分割、总剂量45 Gy的治疗。输尿管D和D的中位数分别为60和42 Gy EQD2。未观察到≥4级毒性反应。3例患者(2%)发生3级输尿管梗阻,其D值分别为121、97和74 Gy EQD2。5例患者(4%)出现任何级别的晚期泌尿系统毒性反应,但其中只有1例超过了108 Gy EQD2的D值。尽管超过了该参数,但共有31例(23%)患者未出现晚期毒性反应。计划输尿管剂量与实际接受的输尿管剂量之间未发现显著差异(D 25 vs 22 Gy EQD2,P = 0.23)。中位随访时间为28个月。
SBRT治疗A-P LN寡转移后3级输尿管毒性反应的发生率较低(2%)。23%的患者违反了已发表的剂量限制但未报告毒性反应,提示可能有其他因素起作用。此外,计划输尿管剂量与实际接受的输尿管剂量之间未发现差异,表明计划剂量是实际接受剂量的可靠估计。