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首页> 外文期刊>Journal of neuro-oncology. >Extended adjuvant temozolomide for treatment of newly diagnosed glioblastoma multiforme
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Extended adjuvant temozolomide for treatment of newly diagnosed glioblastoma multiforme

机译:扩展替莫唑胺辅助治疗新诊断的多形性胶质母细胞瘤

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摘要

The standard of care for newly diagnosed glioblastoma multiforme (GBM) is temozolomide (TMZ) chemotherapy given concurrently with radiation for 6 weeks followed by 6 months of adjuvant TMZ. Originally, patients in Alberta were treated with only six cycles of adjuvant TMZ regardless of clinical status but institutional policy was amended to allow up to 12 cycles of adjuvant therapy for patients experiencing at least stable disease and minimal toxicity. We conducted a population-based analysis to determine if extended adjuvant TMZ treatment (i.e., more than six cycles) confers a survival advantage as compared to the standard six cycles for newly diagnosed GBM patients. Patient data was collected from the Alberta Cancer Registry and patient charts. Progression free-and overall survival was determined in patients receiving six cycles of adjuvant TMZ and compared with that of patients receiving more than six cycles. Patients in whom adjuvant chemotherapy was stopped at cycle six experienced a median survival of 16.5 months, whereas, those who received more than six cycles survived for 24.6 months (p = 0.031). Extended adjuvant therapy was not associated with increased toxicity. In multivariate analysis, adjuvant monthly Temozolomide for more than six cycles was an independent prognostic factor for both progression free-and overall survival. These data suggest extended adjuvant temozolomide (i.e., more than six cycles) should be considered in patients with newly diagnosed GBM.
机译:新诊断的多形性胶质母细胞瘤(GBM)的治疗标准是替莫唑胺(TMZ)化疗,放疗6周,然后再辅以6个月的TMZ。最初,阿尔伯塔省的患者仅接受六个周期的TMZ辅助治疗,而不论其临床状况如何,但已修改了机构政策,允许至少12个周期的辅助治疗用于至少经历稳定疾病且毒性最小的患者。我们进行了基于人群的分析,以确定与新诊断的GBM患者的标准六个周期相比,延长的辅助TMZ治疗(即超过六个周期)是否具有生存优势。患者数据来自艾伯塔省癌症登记处和患者图表。确定接受6个周期的TMZ佐剂的患者的无进展生存期和总生存期,并与接受6个周期以上的患者进行比较。在第六周期停止辅助化疗的患者的中位生存期为16.5个月,而接受六个周期以上的患者的生存期为24.6个月(p = 0.031)。延长的辅助治疗与毒性增加无关。在多变量分析中,每月替莫唑胺辅助治疗超过六个周期是无进展生存期和总体生存期的独立预后因素。这些数据表明,对于新诊断为GBM的患者,应考虑延长替莫唑胺的辅助治疗(即超过六个周期)。

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