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首页> 外文期刊>Neuro-Oncology >Practice changing mature results of RTOG study 9802: another positive PCV trial makes adjuvant chemotherapy part of standard of care in low-grade glioma
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Practice changing mature results of RTOG study 9802: another positive PCV trial makes adjuvant chemotherapy part of standard of care in low-grade glioma

机译:实践改变RTOG研究9802的成熟结果:另一项PCV阳性试验使辅助化疗成为低度神经胶质瘤护理标准的一部分

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摘要

The long-term follow-up of the RTOG 9802 trial that compared 54 Gy of radiotherapy (RT) with the same RT followed by adjuvant procarbazine, CCNU, and vincristine (PCV) chemotherapy in high-risk low-grade glioma shows a major increase in survival after adjuvant PCV chemotherapy. Median overall survival increased from 7.8 years to 13.3 years, with a hazard ratio of death of 0.59 (log rank: P = .002). This increase in survival was observed despite the fact that 77% of patients who progressed after RT alone received salvage chemotherapy. With this outcome, RT + PCV is now to be considered standard of care for low-grade glioma requiring postsurgical adjuvant treatment. Unfortunately, studies on molecular correlates associated with response are still lacking. This is now the third trial showing benefit from the addition of PCV to RT in grade Ⅱ or Ⅲ diffuse glioma. The optimal parameter for selecting patients for adjuvant PCV has not yet been fully elucidated, but several candidate markers have so far emerged. It is still unclear whether temo-zolomide can replace PCV and whether initial management with chemotherapy only is a safe initial treatment. Potentially, that may adversely affect overall survival, but concerns for delayed RT-induced neurotoxicity may limit acceptance of early RT in patients with expected long term survival. The current evidence supports that in future trials, grades Ⅱ and Ⅲ tumors with similar molecular backgrounds should be combined, and trials should focus on molecular glial subtype regardless of grade.
机译:RTOG 9802试验的长期随访结果比较了54 Gy放疗(RT)和相同放疗,再辅以丙卡巴肼,CCNU和长春新碱(PCV)辅助化疗治疗高危低度神经胶质瘤PCV辅助化疗后的生存率。中位总生存期从7.8年增加到13.3年,死亡的危险比为0.59(log rank:P = .002)。尽管仅在放疗后进展的患者中有77%接受了挽救性化疗,但仍观察到存活率的提高。有了这个结果,RT + PCV现在被认为是需要术后辅助治疗的低度神经胶质瘤的标准治疗方法。不幸的是,仍然缺乏与反应相关的分子相关性的研究。现在,这是第三项试验,显示在Ⅱ级或Ⅲ级弥漫性神经胶质瘤中,在逆转录病毒治疗中添加PCV有益。尚未完全阐明选择PCV辅助患者的最佳参数,但到目前为止已经出现了几种候选标记。尚不清楚替莫唑胺是否可以代替PCV,仅通过化学疗法进行初始治疗是否是安全的初始治疗尚不清楚。潜在地,这可能对总体生存产生不利影响,但对延迟的RT诱发的神经毒性的担忧可能会限制预期长期生存的患者接受早期RT。目前的证据支持在将来的试验中,应将具有相似分子背景的Ⅱ级和Ⅲ级肿瘤合并使用,并且无论分级如何,试验都应侧重于分子神经胶质亚型。

著录项

  • 来源
    《Neuro-Oncology》 |2014年第12期|1570-1574|共5页
  • 作者

    Martin J. van den Bent;

  • 作者单位

    Department of Neuro-oncology/Neurology, Erasmus M.C. Cancer Institute, Rotterdam, Netherlands Neuro-Oncology Unit Erasmus MC Cancer Center, Groene Hilledijk 301, 3075EA Rotterdam, the Netherlands;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    chemotherapy; low grade glioma; PCV; temozolomide;

    机译:化学疗法低度神经胶质瘤PCV;替莫唑胺;

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