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首页> 外文期刊>The Canadian Journal of Neurological Sciences: le Journal Canadien des Sciences Neurologiques >Adjuvant chemotherapy for adults with malignant glioma: a systematic review.
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Adjuvant chemotherapy for adults with malignant glioma: a systematic review.

机译:成人恶性神经胶质瘤的辅助化疗:系统评价。

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OBJECTIVE: This systematic review examines the role of chemotherapy following surgery and external beam radiotherapy for adults with newly diagnosed malignant glioma. METHODS: MEDLINE, EMBASE, and the Cochrane Library databases were searched to August 2006 to identify relevant randomized controlled trials (RCTs) and meta-analyses. Proceedings from the 1997 to 2006 annual meetings of the American Society of Clinical Oncology were also searched. RESULTS: Two RCTs reported a survival advantage in favour of radiotherapy with concomitant and adjuvant temozolomide compared with radiotherapy alone in patients with anaplastic astrocytoma or glioblastoma. Twenty-six RCTs and two meta-analyses detected either no advantage or a small survival advantage in favour of adjuvant chemotherapy. CONCLUSION: Concomitant temozolomide during radiotherapy and post-radiation adjuvant temozolomide is recommended for all patients ages 18-70 with newly diagnosed glioblastoma multiforme who are fit for radical therapy (ECOG 0-1).Temozolomide may be considered in other situations (i.e., ECOG 2, biopsy only, age > 70, intermediate grade glioma), but there is no high-level evidence to support this decision. Moreover, there are few data on long-term toxicities or quality of life with temozolomide. Adjuvant chemotherapy may be an option for younger patients with anaplastic (grade 3) astrocytoma and patients with pure or mixed oligodendroglioma. However, there is no evidence of a survival advantage from adjuvant chemotherapy in these patients, and treatment-related adverse effects and their impact upon quality of life are poorly studied. The combination of procarbazine, lomustine, and vincristine (PCV) is not recommended for patients with anaplastic oligodendroglioma and oligoastrocytoma.
机译:目的:本系统综述探讨了新诊断为恶性神经胶质瘤的成年人手术后化学疗法和外照射治疗的作用。方法:检索到2006年8月的MEDLINE,EMBASE和Cochrane库数据库,以鉴定相关的随机对照试验(RCT)和荟萃分析。还检索了1997年至2006年美国临床肿瘤学会年会的论文集。结果:与非放疗性星形细胞瘤或成胶质细胞瘤患者相比,与单独放疗相比,两项随机对照试验报道了在放疗中同时使用替莫唑胺和辅助放疗具有生存优势。 26项RCT和两项荟萃分析显示,辅助化疗无优势或生存优势小。结论:对于所有刚诊断为多形性胶质母细胞瘤的18-70岁,适合进行根治性治疗(ECOG 0-1)的患者,建议放疗期间和替莫唑胺同时放疗后使用替莫唑胺(ECOG 0-1)。在其他情况下(例如ECOG) 2,仅活检,年龄> 70岁,中度神经胶质瘤),但尚无高级证据支持此决定。此外,关于替莫唑胺的长期毒性或生活质量的数据很少。对于年轻的间变性(3级)星形细胞瘤患者和单纯性或混合性少突胶质细胞瘤患者,辅助化疗可能是一种选择。但是,尚无证据表明辅助化疗在这些患者中具有生存优势,并且与治疗相关的不良反应及其对生活质量的影响研究很少。不间断性少突胶质神经胶质瘤和少突星形胶质细胞瘤患者不建议使用丙卡巴肼,洛莫斯汀和长春新碱(PCV)的组合。

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