Conde-Moreno Antonio José, García-Gómez Raquel, Albert-Antequera María, Almendros-Blanco Piedad, De Las Peñas-Bataller Ramón, González-Vidal Verónica, López-Torrecilla José Luis, Ferrer-Albiach Carlos
Consorcio Hospitalario Provincial de Castellón, Avda. Doctor Clarà 19, 12002 Castellón, Spain.
Rep Pract Oncol Radiother. 2015 May-Jun;20(3):231-8. doi: 10.1016/j.rpor.2015.01.004. Epub 2015 Feb 20.
To evaluate the possibility of implementing a new scheme of rescue treatment after relapse or progression of high-grade glioma (HGG) treated at the first-line with bevacizumab and irinotecan (BVZ+CPT11), evaluating the response and toxicity of associating BVZ and fractionated stereotactic radiotherapy (BVZ+FSRT).
We retrospectively analysed data from 59 patients with relapse of HGG. Nine patients with HGG relapse after treatment using the Stupp protocol that were treated with BVZ+CPT11 for progression between July 2007 and August 2012, after which the response was assessed according to the Revised Assessment in Neuro-Oncology (RANO) criteria. BVZ was administered at a dose of 10 mg/kg and FSRT up to a prescribed dose of 30 Gy, 500 cGy per fraction, three days a week. The median follow-up was 38 months.
The treatment was well-tolerated by all patients. The response after nuclear magnetic resonance imaging (MRI) at 3-6 months was progression in two patients, stable disease in four, and three patients had a partial response. The median overall survival (OS) from diagnosis until death or the last control was 36.8 months. The median progression-free survival (PFS) was 10.8 months. The results from tumour sub-group analysis indicated that the PFS was not statistically significant although it seemed that it was higher in grade-III. The OS was higher in grade-III gliomas.
The combination of BVZ+FSRT as a second-line HGG relapse rescue treatment is well-tolerated and seems to offer promising results. We believe that multi-centre prospective studies are needed to determine the long-term efficacy and toxicity of this therapeutic approach.
评估在一线使用贝伐单抗和伊立替康(BVZ+CPT11)治疗的高级别胶质瘤(HGG)复发或进展后实施新的挽救治疗方案的可能性,评估联合使用BVZ和分次立体定向放射治疗(BVZ+FSRT)的疗效和毒性。
我们回顾性分析了59例HGG复发患者的数据。9例使用Stupp方案治疗后复发的HGG患者,于2007年7月至2012年8月期间接受BVZ+CPT11治疗以控制病情进展,之后根据神经肿瘤学修订评估(RANO)标准评估疗效。BVZ的给药剂量为10mg/kg,FSRT的处方剂量达30Gy,每次分割剂量为500cGy,每周三次。中位随访时间为38个月。
所有患者对该治疗耐受性良好。3至6个月时核磁共振成像(MRI)检查结果显示,2例患者病情进展,4例病情稳定,3例部分缓解。从诊断至死亡或最后一次复查的中位总生存期(OS)为36.8个月。中位无进展生存期(PFS)为10.8个月。肿瘤亚组分析结果表明,尽管III级患者的PFS似乎较高,但差异无统计学意义。III级胶质瘤患者的OS更高。
BVZ+FSRT联合方案作为HGG复发的二线挽救治疗耐受性良好,似乎能带来有前景的结果。我们认为需要开展多中心前瞻性研究以确定该治疗方法的长期疗效和毒性。