首页> 外文OA文献 >Fatigue following radiotherapy of low-risk early breast cancer – a randomized controlled trial of intraoperative electron radiotherapy versus standard hypofractionated whole-breast radiotherapy: the COSMOPOLITAN trial (NCT03838419)
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Fatigue following radiotherapy of low-risk early breast cancer – a randomized controlled trial of intraoperative electron radiotherapy versus standard hypofractionated whole-breast radiotherapy: the COSMOPOLITAN trial (NCT03838419)

机译:低风险早期乳腺癌放射治疗后疲劳 - 一种随机对照试验的术中电子放射治疗与标准次级乳房放射治疗:COSOMOPOLITAN试验(NCT03838419)

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摘要

Abstract Background Fatigue is one of the most common and distressing side-effects of breast cancer radiotherapy. According to current guidelines, accelerated partial breast irradiation (APBI) may be considered as an alternative treatment option for women with early-stage low-risk breast cancer. One method for APBI is single-dose intraoperative radiotherapy (IORT) applied directly to the tumor bed during breast conserving surgery (BCS). The COSMOPOLITAN trial therefore aims to analyze the intensity of fatigue following single-shot IORT with electrons (IOERT) compared to conventional hypofractionated whole breast irradiation (WBI) in low risk early breast cancer patients. Methods This trial is conducted as a multicenter, prospective, randomized, two-arm phase II study comparing the intensity of fatigue in early-stage breast cancer (cT1cN0cM0, tumor size  50 years) treated either with WBI or APBI after BCS. Secondary outcomes investigated are tumor control, overall survival (OS), disease-free survival (DFS), acute and chronic toxicity, quality of life (QoL) and cosmesis. A total of 202 patients will be randomized into two arms: Patients in arm A will receive WBI (40.05 Gy, 15 fractions) after surgical resection, while patients in arm B will receive IOERT (21 Gy to the 90%-isodose) during BCS. Fatigue will be assessed 12 weeks post surgery with the help of the Functional Assessment of Chronic Illness Therapy (FACIT) Fatigue Scale. Discussion The present trial aims to evaluate treatment response to compare single-shot intraoperative electron APBI to conventional WBI following BCS in early-stage low risk breast cancer patients. Fatigue is selected as the primary, patient-reported endpoint due its major clinical relevance. Trial registration The study is prospectively registered on February 12th, 2019: Clinicaltrials.gov, NCT03838419 . “Intraoperative Electron Radiotherapy for Low-risk Early Breast Cancer (COSMOPOLITAN)”. Study status Ongoing study. Start of recruitment was December 2019.
机译:摘要背景疲劳是乳腺癌放射疗法最常见和最令人痛苦的副作用之一。根据目前的准则,加速的部分乳房辐射(APBI)可被视为具有早期低风险乳腺癌的妇女的替代治疗选择。用于APBI的一种方法是单剂量术中放射治疗(IORT)在乳房保守手术(BCS)期间直接施加到肿瘤床上。因此,与低风险早期乳腺癌患者中的常规次乳腺辐照(WBI)相比,国际化试验旨在通过电子(IOERT)与电子(IOERT)相比分析单射IITT后的疲劳强度。方法本试验是作为多中心,前瞻性,随机的双臂期II研究,比较BCS后早期乳腺癌(CT1CN0CM0,肿瘤大小50岁)的疲劳强度比较。调查的二次结果是肿瘤对照,整体存活(OS),无病生存(DFS),急性和慢性毒性,寿命质量(QOL)和杂志。共有202名患者将被随机分为两臂:手臂A中的患者会在手术切除后接受WBI(40.05倍,15分),而ARM B中的患者将在BCS期间接受IOERT(21 GY至90%-ISODOSE)。 。疲劳将在手术后12周,促进慢性疾病治疗(FACIT)疲劳规模的功能评估。讨论目前的试验旨在评估治疗响应,以使单次术中电子APBI与早期低风险乳腺癌患者的BCS进行常规WBI。疲劳被选为主要患者报告的终点,其主要临床相关性。审判登记该研究在2019年2月12日上市期刊:Clinicaltrials.gov,NCT03838419。 “低风险早期乳腺癌(国际化学)的术中电子放射治疗。研究状况正在进行的研究。招聘的开始是2019年12月。

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