Department of Radiation Oncology, Ludwig-Maximilians-University, Marchioninistr. 15, 81377, Munich, Germany.
Strahlenther Onkol. 2012 Apr;188(4):328-33. doi: 10.1007/s00066-011-0055-2. Epub 2012 Feb 22.
Most patients with malignant glioma ultimately fail locally or loco-regionally after the first treatment, with re-irradiation being a reasonable treatment option. However, only limited data are presently available allowing for a precise selection of patients suitable for re-treatment with regard to safety and efficacy.
Using the department database, 39 patients with a second course of radiation were identified. Doses to gross tumor volume (GTV), planning target volume (PTV), and relevant organs at risk (OARs; brainstem, optic chiasm, optic nerves, brain) were retrospectively analyzed and correlated to outcome parameters. Relevant treatment parameters including D(max), D(min), D(mean), and volume (ml) were obtained. Equivalent uniform dose (EUD) values were calculated for the tumor and OARs. To address the issue of radiation necrosis/leukoencephalopathy posttherapeutic MRI images were routinely examined every 3 months.
Median follow-up was 147 days. The time interval between first and second irradiation was regularly greater than 6 months. Median EUDs to the OARs were 11.9 Gy (range 0.7-27.4 Gy) to the optic chiasm, 17.6 Gy (range 0.7-43.0 Gy) to the brainstem, 4.9/2.1 Gy (range 0.3-24.5 Gy) to the right/left optic nerve, and 29.4 Gy (range 25.2-32.5 Gy) to the brain. No correlation between treated volume and survival was observed. Cold spots and dose did not correlate with survival. Re-irradiated volumes were treated with on average lower doses if they were larger and vice versa.
In general, re-irradiation is a safe and feasible re-treatment option. No relevant toxicity was observed after re-irradiation in our patient cohort during follow-up. In this regard, this analysis provides baseline data for the selection of putative patients. EUD values are derived and may serve as reference for further studies, including intensity-modulated radiotherapy (IMRT) protocols.
大多数恶性胶质瘤患者在首次治疗后最终会出现局部或局部区域复发,再放疗是一种合理的治疗选择。然而,目前仅有有限的数据可以精确选择适合再治疗的患者,以确保安全性和疗效。
利用科室数据库,我们确定了 39 例接受第二次放疗的患者。回顾性分析了大体肿瘤体积(GTV)、计划靶区(PTV)和相关危及器官(脑干、视交叉、视神经、脑)的剂量,并将其与结果参数相关联。获取了相关治疗参数,包括 D(max)、D(min)、D(mean)和体积(ml)。计算了肿瘤和 OAR 的等效均匀剂量(EUD)值。为了解决治疗后 MRI 图像上的放射性坏死/白质脑病问题,我们每 3 个月常规检查一次。
中位随访时间为 147 天。首次和第二次放疗之间的时间间隔通常大于 6 个月。OAR 的中位 EUD 值为视神经交叉 11.9 Gy(范围 0.7-27.4 Gy),脑干 17.6 Gy(范围 0.7-43.0 Gy),右侧/左侧视神经 4.9/2.1 Gy(范围 0.3-24.5 Gy),大脑 29.4 Gy(范围 25.2-32.5 Gy)。未观察到治疗体积与生存之间的相关性。冷点和剂量与生存无关。如果再照射的体积较大,则给予的剂量平均较低,反之亦然。
一般来说,再放疗是一种安全可行的再治疗选择。在我们的患者队列中,在随访期间,再放疗后没有观察到相关毒性。在这方面,该分析为选择潜在患者提供了基线数据。得出了 EUD 值,可作为进一步研究的参考,包括强度调制放疗(IMRT)方案。