Duke University Medical Center, Durham, NC, USA.
BMC Cancer. 2010 Apr 21;10:155. doi: 10.1186/1471-2407-10-155.
The Lung Cancer Exercise Training Study (LUNGEVITY) is a randomized trial to investigate the efficacy of different types of exercise training on cardiorespiratory fitness (VO2peak), patient-reported outcomes, and the organ components that govern VO2peak in post-operative non-small cell lung cancer (NSCLC) patients.
METHODS/DESIGN: Using a single-center, randomized design, 160 subjects (40 patients/study arm) with histologically confirmed stage I-IIIA NSCLC following curative-intent complete surgical resection at Duke University Medical Center (DUMC) will be potentially eligible for this trial. Following baseline assessments, eligible participants will be randomly assigned to one of four conditions: (1) aerobic training alone, (2) resistance training alone, (3) the combination of aerobic and resistance training, or (4) attention-control (progressive stretching). The ultimate goal for all exercise training groups will be 3 supervised exercise sessions per week an intensity above 70% of the individually determined VO2peak for aerobic training and an intensity between 60 and 80% of one-repetition maximum for resistance training, for 30-45 minutes/session. Progressive stretching will be matched to the exercise groups in terms of program length (i.e., 16 weeks), social interaction (participants will receive one-on-one instruction), and duration (30-45 mins/session). The primary study endpoint is VO2peak. Secondary endpoints include: patient-reported outcomes (PROs) (e.g., quality of life, fatigue, depression, etc.) and organ components of the oxygen cascade (i.e., pulmonary function, cardiac function, skeletal muscle function). All endpoints will be assessed at baseline and postintervention (16 weeks). Substudies will include genetic studies regarding individual responses to an exercise stimulus, theoretical determinants of exercise adherence, examination of the psychological mediators of the exercise - PRO relationship, and exercise-induced changes in gene expression.
VO2peak is becoming increasingly recognized as an outcome of major importance in NSCLC. LUNGEVITY will identify the optimal form of exercise training for NSCLC survivors as well as provide insight into the physiological mechanisms underlying this effect. Overall, this study will contribute to the establishment of clinical exercise therapy rehabilitation guidelines for patients across the entire NSCLC continuum.
NCT00018255.
肺癌运动训练研究(LUNGEVITY)是一项随机试验,旨在研究不同类型的运动训练对心肺功能(VO2peak)、患者报告的结果以及术后非小细胞肺癌(NSCLC)患者决定 VO2peak 的器官成分的疗效。
方法/设计:使用单中心、随机设计,杜克大学医学中心(DUMC)接受根治性完全手术切除的组织学证实的 I 期-IIIA 期 NSCLC 患者 160 例(40 例/研究臂)可能有资格参加本试验。在基线评估后,合格的参与者将被随机分配到以下四种条件之一:(1)单独进行有氧运动,(2)单独进行抗阻训练,(3)有氧运动和抗阻训练的组合,或(4)对照组(渐进式伸展)。所有运动训练组的最终目标是每周进行 3 次监督运动,运动强度高于个体确定的有氧运动 VO2peak 的 70%,抗阻训练强度为 1 次重复最大强度的 60-80%,每次 30-45 分钟/次。渐进式伸展将根据方案长度(即 16 周)、社交互动(参与者将接受一对一指导)和时长(每次 30-45 分钟)与运动组相匹配。主要研究终点为 VO2peak。次要终点包括:患者报告的结果(PRO)(例如,生活质量、疲劳、抑郁等)和氧气级联的器官成分(即肺功能、心功能、骨骼肌功能)。所有终点都将在基线和干预后(16 周)进行评估。子研究将包括关于个体对运动刺激反应的遗传研究、运动依从性的理论决定因素、运动与 PRO 关系的心理中介的检验,以及运动引起的基因表达变化。
VO2peak 作为 NSCLC 的一个重要结局越来越受到重视。LUNGEVITY 将确定 NSCLC 幸存者最佳的运动训练形式,并深入了解这一效应的生理机制。总的来说,这项研究将有助于为整个 NSCLC 连续体的患者建立临床运动治疗康复指南。
NCT00018255。