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本文引用的文献

1
Bevacizumab for the treatment of high-grade glioma: an update after phase III trials.贝伐单抗治疗高级别胶质瘤:III期试验后的最新进展。
Expert Opin Biol Ther. 2014 May;14(5):729-40. doi: 10.1517/14712598.2014.898060. Epub 2014 Mar 22.
2
New molecules and old drugs as emerging approaches to selectively target human glioblastoma cancer stem cells.新型分子与旧药:作为选择性靶向人类胶质母细胞瘤癌症干细胞的新兴方法
Biomed Res Int. 2014;2014:126586. doi: 10.1155/2014/126586. Epub 2014 Jan 2.
3
What have we learned from trials on antiangiogenic agents in glioblastoma?我们从抗血管生成药物治疗胶质母细胞瘤的试验中学到了什么?
Expert Rev Neurother. 2014 Jan;14(1):1-3. doi: 10.1586/14737175.2014.873277.
4
High-grade gliomas: reality and hopes.高级别胶质瘤:现状与希望
Chin J Cancer. 2014 Jan;33(1):1-3. doi: 10.5732/cjc.013.10215.
5
Challenges with the diagnosis and treatment of cerebral radiation necrosis.脑放射性坏死的诊断和治疗挑战。
Int J Radiat Oncol Biol Phys. 2013 Nov 1;87(3):449-57. doi: 10.1016/j.ijrobp.2013.05.015. Epub 2013 Jun 19.
6
Concurrent stereotactic radiosurgery and bevacizumab in recurrent malignant gliomas: a prospective trial.同期立体定向放射外科和贝伐单抗治疗复发性恶性脑胶质瘤:一项前瞻性试验。
Int J Radiat Oncol Biol Phys. 2013 Aug 1;86(5):873-9. doi: 10.1016/j.ijrobp.2013.04.029. Epub 2013 May 29.
7
Patterns of failure after concurrent bevacizumab and hypofractionated stereotactic radiation therapy for recurrent high-grade glioma.贝伐珠单抗联合低分割立体定向放疗治疗复发性高级别胶质瘤后的失败模式。
Int J Radiat Oncol Biol Phys. 2013 Mar 1;85(3):636-42. doi: 10.1016/j.ijrobp.2012.05.031. Epub 2012 Jul 3.
8
Generation and validation of a prognostic score to predict outcome after re-irradiation of recurrent glioma.生成和验证预测复发性脑胶质瘤再放疗后结局的预后评分。
Acta Oncol. 2013 Jan;52(1):147-52. doi: 10.3109/0284186X.2012.692882. Epub 2012 Jun 11.
9
New prognostic factors and calculators for outcome prediction in patients with recurrent glioblastoma: a pooled analysis of EORTC Brain Tumour Group phase I and II clinical trials.复发性胶质母细胞瘤患者预后预测的新预后因素和计算器:EORTC 脑肿瘤组 I 期和 II 期临床试验的汇总分析。
Eur J Cancer. 2012 May;48(8):1176-84. doi: 10.1016/j.ejca.2012.02.004. Epub 2012 Mar 28.
10
A phase II trial of single-agent bevacizumab in patients with recurrent anaplastic glioma.一项单药贝伐珠单抗治疗复发性间变性神经胶质瘤患者的 II 期临床试验。
Neuro Oncol. 2011 Oct;13(10):1143-50. doi: 10.1093/neuonc/nor091. Epub 2011 Aug 24.

在贝伐单抗联合伊立替康治疗出现反应后,采用分割立体定向放射治疗联合贝伐单抗作为高级别胶质瘤的挽救治疗。

Fractionated stereotactic radiotherapy plus bevacizumab after response to bevacizumab plus irinotecan as a rescue treatment for high-grade gliomas.

作者信息

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

机构信息

Consorcio Hospitalario Provincial de Castellón, Avda. Doctor Clarà 19, 12002 Castellón, Spain.

出版信息

Rep Pract Oncol Radiother. 2015 May-Jun;20(3):231-8. doi: 10.1016/j.rpor.2015.01.004. Epub 2015 Feb 20.

DOI:10.1016/j.rpor.2015.01.004
PMID:25949228
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4418580/
Abstract

AIM

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).

MATERIALS AND METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

材料与方法

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。

结果

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。

结论

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。