...
首页> 外文期刊>Journal of radiation oncology >A phase II trial to determine the cosmetic outcomes and toxicity of 27?Gy in five-fraction accelerated partial breast irradiation: the ACCEL trial
【24h】

A phase II trial to determine the cosmetic outcomes and toxicity of 27?Gy in five-fraction accelerated partial breast irradiation: the ACCEL trial

机译:第II期试验,以确定五部分加速部分乳房辐射中的27?GY的化妆品结果和毒性:Accel试验

获取原文
获取原文并翻译 | 示例
           

摘要

Background Accelerated partial breast irradiation (APBI) has been investigated in randomized controlled trials with the goals of reducing side effects and treatment burden. There is accumulating evidence that local control for multi-fraction APBI is not inferior to whole breast irradiation (WBI) but an external beam prescription that can be safely delivered in five consecutive days has not been reported. The aim of this study is to investigate an APBI prescription delivered once per day in 1?week. Methods This is a single-arm, phase II, prospective cohort study. Two hundred seventy-four eligible women with newly diagnosed, early-stage, invasive, or in situ ductal carcinoma treated with breast-conserving surgery and sentinel lymph node biopsy or axillary dissection who are candidates for whole breast radiation without a boost will be recruited. Twenty-seven Gray (Gy) in five fractions will be delivered once daily over five consecutive working days to the target volume. The primary outcome is the rate of global cosmetic deterioration from an excellent or good score at baseline (prior to radiation therapy) to a fair or poor score at 2?years after treatment. The study is powered to demonstrate non-inferiority compared to the use of WBI arm in the RAPID trial. Discussion The ACCEL trial aims to demonstrate the safe and effective delivery of a five-fraction APBI treatment using IMRT or 3D-conformal radiation. The study is designed to account for an updated α/β ratio for breast tissue and compares cosmesis to the WBI arm of the RAPID trial. The ACCEL trial was registered in February 2016 and began accrual in the subsequent May. Conclusions This trial will assess the cosmetic and normal tissue outcomes of external beam APBI delivered in 1?week for early-stage breast cancer. Trial registration Registration number: NCT02681107 ( clinicaltrials.gov ), registered February 2, 2016.
机译:背景技术在随机对照试验中研究了加速的部分乳房辐射(APBI),其具有降低副作用和治疗负担的目标。积累的证据表明,用于多部分APB的局部控制不逊于全乳房辐射(WBI),而是可以在连续五天中安全地交付的外梁处方。本研究的目的是调查每天在1个星期内交付一次APBI处方。方法这是单臂,第二阶段,前瞻性队列研究。招募了两百七十四名合格女性,患有新诊断,早期,侵袭性,或用哺乳淋巴结治疗的原位导管癌,或者是患有全乳房辐射的候选人而没有提升的患者。五个分数中的二十七个灰色(GY)将每天在连续五个工作日内每天递送一次。主要结果是全球化妆品恶化的速度从基线(在放射治疗之前)的优异或良好的分数到2年后的公平或差的分数。与在快速试验中使用WBI ARM相比,该研究得到了不逊断的。讨论Accel试验旨在证明使用IMRT或3D共形辐射的5分数APBI处理的安全有效递送。该研究旨在考虑乳腺组织的更新α/β比,并将杂交与快速试验的WBI臂进行比较。 Accel审判于2016年2月注册,并在随后的5月开始进行应计。结论该试验将评估外部射线APBI的化妆品和正常组织结果,为早期乳腺癌递送1?周。试用登记注册号:NCT02681107(ClinicalTrials.gov),2016年2月2日注册。

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