Department of Radiation Oncology, Washington University in St Louis, St Louis, Missouri.
Department of Medicine, Division of Oncology, Washington University in St Louis, St Louis, Missouri.
Int J Radiat Oncol Biol Phys. 2018 Jun 1;101(2):334-343. doi: 10.1016/j.ijrobp.2018.01.099. Epub 2018 Feb 9.
To analyze the incidence of and risk factors for clinically significant radiation necrosis (cRN) in adult cranial oligodendrogliomas and astrocytomas treated with proton or photon therapy.
Between 2007 and 2015, 160 patients with grade 2 or 3 oligodendrogliomas (with 1p/19q codeletion, n = 53) or astrocytomas (without 1p/19q codeletion, n = 107) were treated with proton (n = 37) or photon (n = 123) therapy. Clinically significant radiation necrosis (RN) was defined as symptomatic RN or asymptomatic RN that resulted in surgery or bevacizumab administration. The cumulative incidence was calculated using competing risks. Risk factors were identified using Cox proportional hazards.
After a median follow-up period of 28.5 months, cRN developed in 18 patients (proton, 6; photon, 12). The 2-year cumulative incidence of cRN for proton and photon therapy was 18.7% (95% confidence interval [CI], 7.5%-33.8%) and 9.7% (95% CI, 5.1%-16%), respectively (P = .16). On multivariate analysis, risk factors for cRN included oligodendroglioma (hazard ratio [HR], 3.57; 95% CI, 1.38-9.25; P = .009) and higher prescription dose (in gray relative biological equivalents [GyRBE]) (HR, 1.30; 95% CI, 1.05-1.61; P = .015). The 2-year cumulative incidence of cRN in oligodendrogliomas and astrocytomas was 24.2% and 6.2%, respectively (P = .01). The relative volume (percentage) of brain receiving 60 GyRBE was a significant dosimetric predictor of cRN in oligodendrogliomas (HR, 1.11; 95% CI, 1.03-1.20; P = .005).
The study showed that 1p/19q codeleted oligodendroglioma was a significant risk factor associated with cRN and the relative volume (percentage) of brain receiving 60 GyRBE was an important dosimetric predictor of cRN for oligodendroglioma patients. There is insufficient evidence at this time to conclude a significant difference in the incidence of cRN between proton and photon therapy.
分析质子或光子放疗治疗成人颅寡突胶质细胞瘤和星形细胞瘤后出现临床显著放射性坏死(cRN)的发生率和危险因素。
在 2007 年至 2015 年间,160 名 2 级或 3 级寡突胶质细胞瘤(1p/19q 缺失,n=53)或星形细胞瘤(无 1p/19q 缺失,n=107)患者接受质子(n=37)或光子(n=123)治疗。临床显著放射性坏死(RN)定义为症状性 RN 或无症状性 RN,导致手术或贝伐单抗治疗。使用竞争风险计算累积发生率。使用 Cox 比例风险识别危险因素。
中位随访 28.5 个月后,18 名患者(质子治疗 6 名,光子治疗 12 名)出现 cRN。质子和光子治疗的 2 年 cRN 累积发生率分别为 18.7%(95%置信区间[CI],7.5%-33.8%)和 9.7%(95%CI,5.1%-16%)(P=.16)。多变量分析显示,cRN 的危险因素包括寡突胶质细胞瘤(风险比[HR],3.57;95%CI,1.38-9.25;P=.009)和更高的处方剂量(格雷氏相对生物等效剂量[GyRBE])(HR,1.30;95%CI,1.05-1.61;P=.015)。寡突胶质细胞瘤和星形细胞瘤的 2 年 cRN 累积发生率分别为 24.2%和 6.2%(P=.01)。接受 60 GyRBE 的大脑相对体积(百分比)是寡突胶质细胞瘤 cRN 的重要剂量学预测因素(HR,1.11;95%CI,1.03-1.20;P=.005)。
该研究表明,1p/19q 缺失的寡突胶质细胞瘤是与 cRN 相关的显著危险因素,接受 60 GyRBE 的大脑相对体积(百分比)是寡突胶质细胞瘤患者 cRN 的重要剂量学预测因素。目前尚无足够证据得出质子和光子治疗的 cRN 发生率存在显著差异的结论。