Department of Radiation Oncology, Centre Léon Bérard, Lyon, France.
Pole of Epidemiology and Biostatistics (EPID), Institut de Recherche Expérimentale et Clinique (IREC), Université Catholique de Louvain, Brussels, Belgium.
J Neurooncol. 2020 Sep;149(3):447-453. doi: 10.1007/s11060-020-03628-z. Epub 2020 Sep 26.
While hypofractionated stereotactic radiotherapy (HFSRT) is being increasingly used for treating brain metastases, clinical data concerning the incidence and risk factors of its main side-effect, namely radiation necrosis (RN), remain limited. In this context, we assessed risk factors of RN in a single center series of patients with brain metastases treated with three common HFSRT dose regimens: 27 Gy in 3 fractions (27 Gy/3#), 30 Gy in 5 fractions (30 Gy/5#), and 35 Gy in 5 fractions (35 Gy/5#).
In total, 360 HFSRT treatments in 294 consecutive patients were retrospectively analysed. Univariable analysis (UVA) and multivariable analysis (MVA) were performed to evaluate the relationship between clinical and dosimetric factors and RN risk.
The 12-month RN rate was 8.8%. On MVA, risk was higher in lesions receiving 27 Gy/3# (HR 3.07 95%CI [1.13;8.36], p = 0.03) and 35 Gy/5# (HR 4.22 95%CI [1.46,12.21], p < 0.01) than in lesions receiving 30 Gy/5#. Risk was also higher in patients having received immunotherapy within 3 months of HFSRT (HR 2.69 95%CI [1.10;6.56], p = 0.03) compared with those who did not. We found no association between RN risk and other tested factors, in particular prior irradiation, lesion histology, lesion location, lesion volume, or brain dosimetric factors.
In the present series, HFSRT was associated with limited RN risk. Incidence of RN was higher with dose regimens delivering a higher biologically effective dose, as well as in patients having received immunotherapy within 3 months of HFSRT.
虽然立体定向放射治疗(SRS)越来越多地用于治疗脑转移瘤,但关于其主要副作用放射性坏死(RN)的发生率和危险因素的临床数据仍然有限。在这种情况下,我们评估了 294 例连续患者的 360 例 SRS 治疗中,3 种常见 SRS 剂量方案(27Gy/3 次分割、30Gy/5 次分割和 35Gy/5 次分割)的患者中 RN 的危险因素。
回顾性分析了 294 例连续患者的 360 例 SRS 治疗。采用单变量分析(UVA)和多变量分析(MVA)评估临床和剂量学因素与 RN 风险的关系。
12 个月时的 RN 发生率为 8.8%。在 MVA 中,与接受 30Gy/5 次分割的病变相比,接受 27Gy/3 次分割(HR3.0795%CI[1.13;8.36],p=0.03)和 35Gy/5 次分割(HR4.2295%CI[1.46,12.21],p<0.01)的病变的风险更高。与未接受免疫治疗的患者相比,在 SRS 后 3 个月内接受免疫治疗的患者(HR2.6995%CI[1.10;6.56],p=0.03)的风险更高。我们没有发现 RN 风险与其他测试因素之间存在关联,特别是既往放疗、病变组织学、病变位置、病变体积或脑部剂量学因素。
在本系列中,SRS 与有限的 RN 风险相关。与给予更高生物有效剂量的剂量方案相比,RN 的发生率更高,并且在 SRS 后 3 个月内接受免疫治疗的患者中也更高。