...
首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >Compliance to the prescribed dose and overall treatment time in five randomized clinical trials of altered fractionation in radiotherapy for head-and-neck carcinomas.
【24h】

Compliance to the prescribed dose and overall treatment time in five randomized clinical trials of altered fractionation in radiotherapy for head-and-neck carcinomas.

机译:在头颈癌放疗中改变分馏的五项随机临床试验中,符合处方剂量和总治疗时间。

获取原文
获取原文并翻译 | 示例

摘要

PURPOSE: To investigate compliance to the prescribed dose-fractionation schedule in five randomized controlled trials of altered fractionation in radiotherapy for head-and-neck carcinoma. METHODS AND MATERIALS: Individual patient data from 2566 patients participating in the European Organization for Research and Treatment of Cancer (EORTC) 22791, EORTC 22811, EORTC 22851, Princess Margaret Hospital (PMH), and continuous hyperfractionated accelerated radiotherapy (CHART) head-and-neck trials were merged in the fractionation IMPACT (Intergroup Merger of Patient data from Altered or Conventional Treatment schedules) study database. The ideal treatment time was defined as the minimum time required to deliver a prescribed schedule. Compliance to the prescribed overall treatment time was quantified as the difference between the actual and the ideal overall time. An overall measure of compliance in an individual patient, the total dose lost (TDL), was calculated as the dose lost due to prolongation of therapy(assuming a D(prolif) of 0.64 Gy/day) plus the difference between the prescribed and the actual dose given. RESULTS: The time in excess of the ideal ranged up to 97 days (average 3.9 days), and 25% of the patients had delays of 6 days or more. World Health Organization (WHO) performance status and nodal stage had a significant effect on TDL. TDL was significantly higher in the conventional than in the altered arm of the EORTC 22851 and CHART trials. In the PMH trial, TDL was significantly higher in the hyperfractionation than in the conventional arm. Centers participating in the three EORTC trials varied significantly in their compliance. There was a significant improvement in compliance in patients treated more recently. CONCLUSIONS: Even in randomized controlled trials, compliance to the prescribed radiation therapy schedule may be relatively poor, especially after conventional fractionation. This affects the interpretation of the outcome of these trials.
机译:目的:在头颈癌放疗中改变分馏的五项随机对照试验中,研究是否符合规定的剂量分馏方案。方法和材料:来自2566名患者的个体患者数据,这些患者参加了欧洲癌症研究和治疗组织(EORTC)22791,EORTC 22811,EORTC 22851,玛格丽特公主医院(PMH)和连续超分割加速放疗(CHART)颈项试验合并在分级IMPACT(来自变更或常规治疗方案的患者数据的组间合并)研究数据库中。理想的治疗时间定义为达到规定时间表所需的最短时间。将对规定的总治疗时间的依从性量化为实际总时间与理想总时间之间的差。个体患者依从性的总体衡量标准,即总剂量损失(TDL),计算为因治疗时间延长而导致的剂量损失(假设D(prolif)为0.64 Gy /天)加上处方药与药物治疗之间的差给出的实际剂量。结果:超过理想时间的时间最长为97天(平均3.9天),并且25%的患者延迟了6天或更长时间。世界卫生组织(WHO)的表现状态和结节阶段对TDL有重大影响。与常规的EORTC 22851和CHART试验相比,TDL显着高于传统方法。在PMH试验中,超分割患者的TDL明显高于常规患者。参加这三项EORTC试验的中心的依从性差异很大。最近接受治疗的患者的依从性有了显着改善。结论:即使在随机对照试验中,对规定的放射治疗方案的依从性也可能相对较差,尤其是在常规分割之后。这影响了这些试验结果的解释。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号