Perry James, Laperriere Normand, Zuraw Lisa, Chambers Alexandra, Spithoff Karen, Cairncross J Gregory
Odette Cancer Centre, Sunnybrook Health Sciences Centre Toronto, Ontario, Canada.
Can J Neurol Sci. 2007 Nov;34(4):402-10. doi: 10.1017/s0317167100007265.
This systematic review examines the role of chemotherapy following surgery and external beam radiotherapy for adults with newly diagnosed malignant glioma.
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.
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.
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.
本系统评价探讨了手术及外照射放疗后化疗在新诊断的成年恶性胶质瘤患者中的作用。
检索MEDLINE、EMBASE和Cochrane图书馆数据库至2006年8月,以识别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会议记录。
两项RCT报告,与单纯放疗相比,同步和辅助使用替莫唑胺的放疗对间变性星形细胞瘤或胶质母细胞瘤患者有生存优势。26项RCT和两项荟萃分析未发现辅助化疗有优势或仅有微小的生存优势。
对于所有年龄在18 - 70岁、新诊断为多形性胶质母细胞瘤且适合根治性治疗(东部肿瘤协作组体能状态0 - 1)的患者,建议在放疗期间同步使用替莫唑胺以及放疗后辅助使用替莫唑胺。在其他情况下(即东部肿瘤协作组体能状态2、仅活检、年龄>70岁、间级胶质瘤)可考虑使用替莫唑胺,但尚无高级别证据支持这一决定。此外,关于替莫唑胺的长期毒性或生活质量的数据很少。辅助化疗可能是年轻的间变性(3级)星形细胞瘤患者以及纯或混合性少突胶质细胞瘤患者的一种选择。然而,在这些患者中尚无证据表明辅助化疗有生存优势,且对治疗相关不良反应及其对生活质量的影响研究不足。不推荐对间变性少突胶质细胞瘤和少突星形细胞瘤患者使用丙卡巴肼、洛莫司汀和长春新碱(PCV)联合方案。