Department of Radiation Oncology, University of Toronto, Toronto, Ontario, Canada; Radiation Medicine Program, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Department of Biostatistics, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Int J Radiat Oncol Biol Phys. 2018 Jul 1;101(3):574-580. doi: 10.1016/j.ijrobp.2018.02.025. Epub 2018 Mar 2.
To explore and quantify the relationship between esophageal dose and toxicity in the setting of lung stereotactic body radiation therapy (SBRT).
This analysis was conducted on the basis of a prospective study of patients treated with SBRT at our institution from October 2004 to December 2015. Most patients were treated with 54 Gy/3 fractions, 48 Gy/4 fractions alternate days, or 60 Gy/8 fractions daily. Toxicity was prospectively graded using Common Terminology Criteria for Adverse Events version 3.0. Logistic regression was used to estimate the risk of esophageal toxicity as a function of radiation therapy dose, in 2-Gy-equivalent dose, using an α/β ratio of 3 Gy in the linear-quadratic model.
A total of 632 patients were analyzed. The median follow-up was 20.8 months. Median overall survival was 35.3 months. The rate of late or acute grade ≥1 esophageal toxicity, including dysphagia, odynophagia, and esophagitis, was 3.3% (n = 21). The median (range) esophageal doses were 11.8 Gy (0.2-48.2 Gy), 10.34 Gy (0.17-44.5 Gy), and 9.63 Gy (0.08-43 Gy) for Dmax, D1cc, and D2cc, respectively. A 15% risk of esophageal toxicity was associated with a 2-Gy-equivalent dose of Dmax 141.6 Gy, D1cc 123.61 Gy, and D2cc 117.6 Gy. Of the 21 patients who experienced esophageal toxicity, only 1 patient had grade 3 toxicity, and the remainder had grade 2 or lower toxicity.
The observed rate of toxicity was low, despite some patients receiving relatively high doses to the esophagus. A prospective study in a targeted population, for example patients with ultracentral tumors, may provide more accurate dose-toxicity parameters.
探讨并量化肺立体定向体部放射治疗(SBRT)中食管剂量与毒性之间的关系。
本分析基于对 2004 年 10 月至 2015 年 12 月在本机构接受 SBRT 治疗的患者进行的前瞻性研究。大多数患者接受 54Gy/3 个剂量、48Gy/4 个剂量隔日或 60Gy/8 个剂量每日治疗。采用不良事件通用术语标准 3.0 版前瞻性分级毒性。使用线性二次模型中 3Gy 的α/β 比,对数回归估计食管毒性风险作为放疗剂量(2Gy 等效剂量)的函数。
共分析了 632 例患者。中位随访时间为 20.8 个月。中位总生存期为 35.3 个月。迟发性或急性≥1 级食管毒性(包括吞咽困难、咽痛和食管炎)的发生率为 3.3%(n=21)。Dmax、D1cc 和 D2cc 的中位(范围)食管剂量分别为 11.8Gy(0.2-48.2Gy)、10.34Gy(0.17-44.5Gy)和 9.63Gy(0.08-43Gy)。食管毒性风险增加 15%与 Dmax 141.6Gy、D1cc 123.61Gy 和 D2cc 117.6Gy 的 2Gy 等效剂量相关。在 21 例发生食管毒性的患者中,仅 1 例为 3 级毒性,其余为 2 级或更低级毒性。
尽管一些患者接受了相对较高的食管剂量,但观察到的毒性发生率较低。针对特定人群(例如超中心肿瘤患者)的前瞻性研究可能提供更准确的剂量-毒性参数。