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[胶质瘤的管理]

[Management of gliomas].

作者信息

Lévy S, Chapet S, Mazeron J-J

机构信息

Service de radiothérapie oncologique, centre Henry-Kaplan, université François-Rabelais, CHRU de Tours, 2, boulevard Tonnelé, 37000 Tours, France.

Service de radiothérapie oncologique, groupe hospitalier Pitié-Salpêtrière, 47-83, boulevard de l'Hôpital, 75651 Paris cedex, France; Université Paris VI, 75651 Paris cedex, France.

出版信息

Cancer Radiother. 2014 Oct;18(5-6):461-7. doi: 10.1016/j.canrad.2014.07.147. Epub 2014 Sep 4.

DOI:10.1016/j.canrad.2014.07.147
PMID:25201633
Abstract

Gliomas are the most frequent primary brain tumors. Their care is difficult because of the proximity of organs at risk. The treatment of glioblastoma includes surgery followed by chemoradiation with the protocol of Stupp et al. The addition of bevacizumab allows an increase in progression-free survival by 4 months but it does not improve overall survival. This treatment is reserved for clinical trials. Intensity modulation radiotherapy may be useful to reduce the neurocognitive late effects in different types of gliomas. In elderly patients an accelerated radiotherapy 40 Gy in 15 fractions allows a similar survival to standard radiotherapy. O(6)-methylguanine-DNA methyltransferase (MGMT) status may help to choose between chemotherapy and radiotherapy. There is no standard for the treatment of recurrent gliomas. Re-irradiation in stereotactic conditions allows a median survival of 8 to 12.4 months. Anaplastic gliomas with 1p19q mutation have a greater sensibility to chemotherapy by procarbazine, lomustine and vincristine. Chemoradiotherapy in these patients has become the standard treatment. Many studies are underway testing targeted therapies, their place in the therapeutic management and new radiotherapy techniques.

摘要

胶质瘤是最常见的原发性脑肿瘤。由于临近危险器官,其治疗颇具难度。胶质母细胞瘤的治疗包括手术,随后按照Stupp等人的方案进行放化疗。添加贝伐单抗可使无进展生存期延长4个月,但并不能改善总生存期。这种治疗方法仅用于临床试验。调强放疗可能有助于减少不同类型胶质瘤的神经认知晚期效应。在老年患者中,15次分割给予40 Gy的加速放疗可获得与标准放疗相似的生存期。O(6)-甲基鸟嘌呤-DNA甲基转移酶(MGMT)状态可能有助于在化疗和放疗之间做出选择。复发性胶质瘤的治疗尚无标准方案。立体定向条件下的再放疗可使中位生存期达到8至12.4个月。具有1p19q突变的间变性胶质瘤对丙卡巴肼、洛莫司汀和长春新碱化疗更敏感。这些患者的放化疗已成为标准治疗方法。目前正在进行许多研究,测试靶向治疗、其在治疗管理中的地位以及新的放疗技术。

相似文献

1
[Management of gliomas].[胶质瘤的管理]
Cancer Radiother. 2014 Oct;18(5-6):461-7. doi: 10.1016/j.canrad.2014.07.147. Epub 2014 Sep 4.
2
NOA-04 randomized phase III trial of sequential radiochemotherapy of anaplastic glioma with procarbazine, lomustine, and vincristine or temozolomide.NOA-04 间变性胶质瘤序贯放化疗(采用丙卡巴肼、洛莫司汀和长春新碱或替莫唑胺)的随机 III 期试验
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Impact of 1p/19q codeletion and histology on outcomes of anaplastic gliomas treated with radiation therapy and temozolomide.1p/19q 联合缺失与组织学特征对放化疗治疗间变性神经胶质瘤患者预后的影响。
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Regimen of procarbazine, lomustine, and vincristine versus temozolomide for gliomas.丙卡巴肼、洛莫司汀和长春新碱方案与替莫唑胺治疗胶质瘤的对比
Cancer. 2018 Jul 1;124(13):2674-2676. doi: 10.1002/cncr.31371. Epub 2018 Apr 26.
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Anaplastic glioma: how to prognosticate outcome and choose a treatment strategy. [corrected].间变性胶质瘤:如何预测预后及选择治疗策略。[已校正]
J Clin Oncol. 2009 Dec 10;27(35):5861-2. doi: 10.1200/JCO.2009.24.5985. Epub 2009 Nov 9.
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Treating anaplastic oligodendrogliomas and WHO grade 2 gliomas: PCV or temozolomide? The case for PCV.治疗间变性少突胶质细胞瘤和世界卫生组织2级胶质瘤:PCV方案还是替莫唑胺?支持PCV方案的理由。
Oncology (Williston Park). 2015 Apr;29(4):264, 266-8.
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Adults with newly diagnosed high-grade gliomas.新诊断为高级别胶质瘤的成年人。
Curr Treat Options Oncol. 2001 Dec;2(6):507-15. doi: 10.1007/s11864-001-0072-y.
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Treating anaplastic oligodendrogliomas and WHO grade 2 gliomas: PCV or temozolomide? The case for temozolomide.治疗间变性少突胶质细胞瘤和世界卫生组织2级胶质瘤:PCV方案还是替莫唑胺?替莫唑胺的情况
Oncology (Williston Park). 2015 Apr;29(4):265, 275.
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O(6) -methylguanine-DNA methyltransferase (MGMT) promoter methylation and low MGMT-encoded protein expression as prognostic markers in glioblastoma patients treated with biodegradable carmustine wafer implants after initial surgery followed by radiotherapy with concomitant and adjuvant temozolomide.O(6)-甲基鸟嘌呤-DNA 甲基转移酶(MGMT)启动子甲基化和低 MGMT 编码蛋白表达作为初始手术后行放疗联合替莫唑胺辅助治疗的胶质母细胞瘤患者的预后标志物,治疗中使用了可生物降解的卡莫司汀植入物。
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[Clinicopathological diagnosis of gliomas by genotype analysis].[通过基因分型分析对胶质瘤进行临床病理诊断]
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引用本文的文献

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Characterizing nanoscale changes in the activity of VEGFR-2 on glioma microvascular endothelial cell membranes using atomic force microscopy.使用原子力显微镜表征胶质瘤微血管内皮细胞膜上VEGFR-2活性的纳米级变化。
Exp Ther Med. 2017 Feb;13(2):483-488. doi: 10.3892/etm.2016.4014. Epub 2016 Dec 29.
2
Long-term survival in glioblastoma: methyl guanine methyl transferase (MGMT) promoter methylation as independent favourable prognostic factor.胶质母细胞瘤的长期生存:甲基鸟嘌呤甲基转移酶(MGMT)启动子甲基化作为独立的有利预后因素。
Radiol Oncol. 2016 Nov 10;50(4):394-401. doi: 10.1515/raon-2015-0041. eCollection 2016 Dec 1.