Department of Radiation Oncology, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-ku, Osaka 541-8567, Japan.
Department of Neurosurgery, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-ku, Osaka 541-8567, Japan.
J Radiat Res. 2024 Sep 24;65(5):658-666. doi: 10.1093/jrr/rrae057.
Brainstem metastases are challenging to manage owing to the critical neurological structures involved. Although stereotactic radiotherapy (SRT) offers targeted high doses while minimizing damage to adjacent normal tissues, the optimal dose fractionation remains undefined. This study evaluated the efficacy and safety of multifraction SRT with an inhomogeneous dose distribution. This retrospective study included 31 patients who underwent 33 treatments for 35 brainstem lesions using linear accelerator-based multifraction SRT (30 Gy in five fractions, 35 Gy in five fractions or 42 Gy in 10 fractions) with an inhomogeneous dose distribution (median isodose, 51.9%). The outcomes of interest were local failure, toxicity and symptomatic failure. The median follow-up time after brainstem SRT for a lesion was 18.6 months (interquartile range, 10.0-24.3 months; range, 1.8-39.0 months). Grade 2 toxicities were observed in two lesions, and local failure occurred in three lesions. No grade 3 or higher toxicities were observed. The 1-year local and symptomatic failure rates were 8.8 and 16.7%, respectively. Toxicity was observed in two of seven treatments with a gross tumor volume (GTV) greater than 1 cc, whereas no toxicity was observed in treatments with a GTV less than 1 cc. No clear association was observed between the biologically effective dose of the maximum brainstem dose and the occurrence of toxicity. Our findings indicate that multifraction SRT with an inhomogeneous dose distribution offers a favorable balance between local control and toxicity in brainstem metastases. Larger multicenter studies are needed to validate these results and determine the optimal dose fractionation.
脑干部位转移瘤的治疗颇具挑战,因为此处存在重要的神经结构。虽然立体定向放射治疗(SRT)可提供靶向高剂量,同时最大限度减少对相邻正常组织的损伤,但最佳分割剂量仍未确定。本研究评估了不均匀剂量分布的多次分割 SRT 的疗效和安全性。本回顾性研究纳入了 31 名患者,共 35 个脑干部位病变接受了基于直线加速器的多次分割 SRT 治疗(30Gy/5 次、35Gy/5 次或 42Gy/10 次),剂量分布不均匀(中位数等剂量为 51.9%)。主要观察终点为局部失败、毒性和症状性失败。脑干部位 SRT 后病变的中位随访时间为 18.6 个月(四分位间距,10.0-24.3 个月;范围,1.8-39.0 个月)。2 个病变观察到 2 级毒性,3 个病变出现局部失败。未观察到 3 级或更高级别的毒性。1 年局部和症状性失败率分别为 8.8%和 16.7%。GTV 大于 1cc 的 7 次治疗中有 2 次观察到毒性,而 GTV 小于 1cc 的治疗中未观察到毒性。未观察到最大脑干剂量的生物有效剂量与毒性发生之间存在明确关联。我们的研究结果表明,不均匀剂量分布的多次分割 SRT 在脑转移瘤中提供了局部控制和毒性之间的良好平衡。需要更大规模的多中心研究来验证这些结果并确定最佳分割剂量。