首页> 美国卫生研究院文献>other >NCOG-01. PRESERVATION OF NEUROCOGNITIVE FUNCTION (NCF) WITH HIPPOCAMPAL AVOIDANCE DURING WHOLE-BRAIN RADIOTHERAPY (WBRT) FOR BRAIN METASTASES: PRELIMINARY RESULTS OF PHASE III TRIAL NRG ONCOLOGY CC001
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NCOG-01. PRESERVATION OF NEUROCOGNITIVE FUNCTION (NCF) WITH HIPPOCAMPAL AVOIDANCE DURING WHOLE-BRAIN RADIOTHERAPY (WBRT) FOR BRAIN METASTASES: PRELIMINARY RESULTS OF PHASE III TRIAL NRG ONCOLOGY CC001

机译:NCOG-01。全脑放疗(WBRT)期间脑转移瘤伴海马回避的神经认知功能(NCF)的保存:III期试验NRG肿瘤学CC001的初步结果

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摘要

PURPOSE: NRG CC001, a phase III trial of WBRT plus memantine with or without hippocampal avoidance, sought to evaluate the neuro-protective effects of avoiding the hippocampus using intensity-modulated radiotherapy.METHODSAdult patients with brain metastases were stratified by RPA class and receipt of prior radiosurgery/surgery and randomized to WBRT+memantine (WBRT+M) versus hippocampal-avoidant WBRT+memantine (HA-WBRT+M) (30Gy in 10 fractions). Standardized NCF tests were performed at baseline, 2, 4, 6, and 12 months. The primary endpoint was time to NCF failure, defined as decline on at least one of the following tests using the reliable change index: Hopkins Verbal Learning Test-Revised, Trail Making Test, or Controlled Oral Word Association. Cumulative incidence was used to estimate time to NCF failure (death without NCF failure was treated as competing risk) with between-arms differences tested using Grays test. To detect an 11% absolute reduction in 6-month NCF failure, 382 analyzable patients were required for 90% power with two-sided =0.05. Due to possible non-compliance, the sample size was increased by 25% (510 patients).
机译:目的:NRG CC001是一项WBRT加美金刚治疗或不进行海马避免的III期临床试验,旨在评估采用强度调节放疗避免海马的神经保护作用。既往放射外科/外科手术,随机分为WBRT +美金刚(WBRT + M)与避免海马的WBRT +美金刚(HA-WBRT + M)(10份30Gy)。在基线,第2、4、6和12个月进行标准化的NCF测试。主要终点是发生NCF失败的时间,其定义为使用可靠的变更指数在以下至少一项测试中下降:霍普金斯言语学习修订版(Hopkins Verbal Learning Test-Revised),追踪制作测试(Trail Making Test)或受控口语协会(Controlled Oral Word Association)。累积发生率用于估计NCF失败的时间(无NCF失败的死亡被视为竞争风险),而手臂之间的差异使用Grays检验进行了测试。为了检测6个月NCF衰竭绝对减少11%,需要382位可分析的患者进行90%的能量检查,两侧= 0.05。由于可能不符合规定,样本量增加了25%(510位患者)。

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