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Neo-train:一项双臂随机对照试验的研究方案和可行性结果,旨在探讨新辅助化疗期间监督下运动对乳腺癌患者肿瘤反应的影响

英文原题:Neo-train: study protocol and feasibility results for a two-arm randomized controlled trial investigating the effect of supervised exercise during neoadjuvant chemotherapy on tumour response in patients with breast cancer.

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Neo-train: study protocol and feasibility results for a two-arm randomized controlled trial investigating the effect of supervised exercise during neoadjuvant chemotherapy on tumour response in patients with breast cancer.

PubMed 2023/08/19(内容时间) BMC Cancer Q2 · IF 4.1(JCR 2025)

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研究概要

本研究将为乳腺癌患者在接受 NACT 的同时进行监督下有氧和抗阻运动对肿瘤反应和肿瘤微环境的潜在益处提供新颖且重要的数据,这些数据对生存率和复发风险可能具有重要意义。

中文摘要

新辅助化疗(NACT)期间开展运动干预进行预康复,可有效减少癌症患者化疗相关躯体和心理社会不良事件。临床前研究也支持有氧运动可抑制肿瘤微环境生长,并可能改善化疗药物递送,但在人类患者中的证据有限。本研究旨在考察NACT期间开展有监督的高强度有氧和抗阻训练能否促进乳腺癌肿瘤缩小。

这项平行两组随机对照试验计划纳入120名年满18岁、在丹麦一家大学医院新诊断乳腺癌并开始标准NACT的女性(根据效能计算需90名受试者,并预留25%,即30名脱落)。受试者随机接受常规照护,或参与有监督的运动项目:在固定自行车上进行高强度间歇训练,并使用器械开展渐进式抗阻训练,每周3次,持续24周,与NACT同期进行;另依据筛查结果,建议中重度心理困扰者寻求咨询(Neo-Train项目)。主要结局为手术前MRI测量的肿瘤大小变化(最大病灶的最大直径,单位毫米)。次要结局包括临床/病理学、躯体和患者报告指标,例如NACT相对剂量强度、住院、身体组成、体能、肌力、健康相关生活质量、一般焦虑和抑郁;还包括肿瘤内血管性、TIL(肿瘤浸润淋巴细胞)、循环肿瘤DNA和血液生化等生物学指标。测量时间点为基线(NACT开始前1周至开始后1–2周)、NACT期间(约第7、13和19周)、术前(约第21–29周)、手术时(约第21–30周)和术后3个月(基线后约第33–42周)。 讨论:本研究将提供新的重要数据,评估NACT期间同步开展有监督的有氧和抗阻运动对乳腺癌患者肿瘤应答和肿瘤微环境的潜在益处,并探讨其对生存和复发风险的意义。如果运动干预有效,本研究有望推动将运动作为新辅助治疗策略中的积极组成部分。 试验注册:2020年11月10日在ClinicalTrials.gov注册(NCT04623554)。

展开英文摘要原文

Prehabilitation with exercise interventions during neoadjuvant chemotherapy (NACT) is effective in reducing physical and psychosocial chemotherapy-related adverse events in patients with cancer. In preclinical studies, data also support a growth inhibitory effect of aerobic exercise on the tumour microenvironment with possible improved chemotherapy delivery but evidence in human patients is limited. The aim of the study here described is to investigate if supervised exercise with high-intensity aerobic and resistance training during NACT can improve tumour reduction in patients with breast cancer.

This parallel two-armed randomized controlled trial is planned to include 120 women aged ≥ 18 years with newly diagnosed breast cancer starting standard NACT at a university hospital in Denmark (a total of 90 participants needed according to the power calculation and allowing 25% (n = 30) dropout). The participants will be randomized to usual care or supervised exercise consisting of high-intensity interval training on a stationary exercise bike and machine-based progressive resistance training offered three times a week for 24 weeks during NACT, and screening-based advice to seek counselling in case of moderate-severe psychological distress (Neo-Train program). The primary outcome is tumour size change (maximum diameter of the largest lesion in millimetre) measured by magnetic resonance imaging prior to surgery. Secondary outcomes include clinical/pathological, physical and patient-reported measures such as relative dose intensity of NACT, hospital admissions, body composition, physical fitness, muscle strength, health-related quality of life, general anxiety, depression, and biological measures such as intratumoural vascularity, tumour infiltrating lymphocytes, circulating tumour DNA and blood chemistry. Outcomes will be measured at baseline (one week before to 1-2 weeks after starting NACT), during NACT (approximately week 7, 13 and 19), pre-surgery (approximately week 21-29), at surgery (approximately week 21-30) and 3 months post-surgery (approximately 33-42 weeks from baseline). DISCUSSION: This study will provide novel and important data on the potential benefits of supervised aerobic and resistance exercise concomitant to NACT on tumour response and the tumour microenvironment in patients with breast cancer, with potential importance for survival and risk of recurrence. If effective, our study may help increase focus of exercise as an active part of the neoadjuvant treatment strategy. TRIAL REGISTRATION: The trial was registered at ClinicalTrials.gov (NCT04623554) on November 10, 2020.

论文信息

作者
Kjeldsted E、Ammitzbøll G、Jørgensen LB、Lodin A、Bojesen RD、Ceballos SG、Rosthøj S、Lænkholm AV
单位
Department of Clinical Oncology and Palliative Care, Zealand University Hospital, Rådmannsengen 5, Naestved, 4700, Denmark. evakj@regionsjaelland.dk.Denmark
文献类型
临床试验方案
期刊
BMC cancer2023 Aug 19
原文标识
PubMed 37598196 · DOI 10.1186/s12885-023-11284-5