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胶质母细胞瘤治疗的现状与展望

State of the art and perspectives in the treatment of glioblastoma.

作者信息

Grimm Sean A, Chamberlain Marc C

机构信息

Department of Neurology, Northwestern University, Feinberg School of Medicine, Chicago, IL 60611, USA.

出版信息

CNS Oncol. 2012 Sep;1(1):49-70. doi: 10.2217/cns.12.5.

Abstract

Glioblastoma is the most common malignant primary brain tumor. Cures are rare and median survival varies from several to 22 months. Standard treatment for good performance patients consists of maximal safe surgical resection followed by radiotherapy with concurrent temozolomide (TMZ) chemotherapy and six cycles of postradiotherapy TMZ. At recurrence, treatment options include repeat surgery (with or without Gliadel wafer placement), reirradiation or systemic therapy. Most patients with good performance status are treated with cytotoxic chemotherapy or targeted biologic therapy following or in lieu of repeat surgery. Cytotoxic chemotherapy options include nitrosoureas, rechallenge with TMZ, platins, phophoramides and topoisomerase inhibitors, although efficacy is limited. Despite the intense effort of developing biologic agents that target angiogenesis and growth and proliferative pathways, bevacizumab is the only agent that has shown efficacy in clinical trials. It was awarded accelerated approval in the USA after demonstrating an impressive radiographic response in two open-label, prospective Phase II studies. Two randomized, Phase III trials of upfront bevacizumab have completed and may demonstrate survival benefit; however, results are pending at this time. Given the limited treatment options at tumor recurrence, consideration for enrollment on a clinical trial is encouraged.

摘要

胶质母细胞瘤是最常见的原发性恶性脑肿瘤。治愈情况罕见,中位生存期从几个月到22个月不等。对于身体状况良好的患者,标准治疗包括最大安全限度的手术切除,随后进行放疗并同步使用替莫唑胺(TMZ)化疗以及六个周期的放疗后TMZ治疗。复发时,治疗选择包括再次手术(有无放置Gliadel薄片)、再次放疗或全身治疗。大多数身体状况良好的患者在再次手术之后或不进行再次手术时接受细胞毒性化疗或靶向生物治疗。细胞毒性化疗选择包括亚硝基脲类、再次使用TMZ、铂类、磷酰胺类和拓扑异构酶抑制剂,尽管疗效有限。尽管在开发针对血管生成以及生长和增殖途径的生物制剂方面付出了巨大努力,但贝伐单抗是唯一在临床试验中显示出疗效的药物。在两项开放标签的前瞻性II期研究中显示出令人印象深刻的影像学反应后,它在美国获得了加速批准。两项关于一线使用贝伐单抗的随机III期试验已经完成,可能会证明其生存获益;然而,目前结果尚未公布。鉴于肿瘤复发时治疗选择有限,鼓励考虑参加临床试验。

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