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临床试验/NCT02006979
NCT02006979已完成1 期

The Effects of Exercise Before Doxorubicin Chemotherapy on Cardiac Function

University of British Columbia1 个研究点 分布在 1 个国家目标入组 27 人开始时间: 2016年1月15日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
27
试验地点
1
主要终点
Global Longitudinal Strain

研究概览

简要总结

In rodents, a single bout of exercise prior to injection of a chemotherapy agent used to treat breast cancer prevents or attenuates a number of markers of cardiac injury. This study will investigate whether this finding translates to human breast cancer patients. Participants scheduled to receive chemotherapy for breast cancer will be randomized to exercise or no exercise 24 hours prior to every chemotherapy treatment. The effect on cardiac function will be compared between groups noninvasively by echocardiography and electrocardiography and a venous blood draw at baseline before chemotherapy, after the first treatment and at the end of chemotherapy.

详细描述

  1. Purpose The purpose of this study is to investigate whether performing a single bout of exercise 24 hours prior to receiving infusions of the anthracycline chemotherapy agent doxorubicin for breast cancer can prevent some of the damaging cardiac effects. Currently, doxorubicin is the most effective chemotherapy agent for breast cancer but is also the most damaging. As such, increased risk of cardiovascular disease is a growing concern in doxorubicin-treated patients. Current strategies for minimizing cardiac injury are dose reduction and discontinuation of therapy, which compromise the effectiveness of the treatment. Interventions that can minimize the cardiac injury associated with doxorubicin could reduce cancer-related and cardiovascular disease-related mortality in women diagnosed with breast cancer.

  2. Hypotheses 1. Performing an acute bout of exercise within 24 hours before anthracycline infusion will decrease the acute negative change in subclinical markers of cardiotoxicity after the first anthracycline infusion seen in those who do not exercise for 72 hours prior.

  3. Performing exercise within 24 hours before every infusion of anthracycline will decrease the negative change in markers of cardiac dysfunction seen at the end of chemotherapy in those who do not exercise for 72 hours prior to each infusion.

  1. Justification An acute exercise bout prior to induction of a myocardial infarction in animals provides cardioprotective benefit by reducing the size of the infarct relative to control animals. Recently, acute exercise performed 24 hours before anthracycline injection in rodents has also provided a cardioprotective benefit. Oxidative stress and apoptosis of cardiomyocyte mitochondria are primary mechanisms of anthracycline-induced cardiotoxicity. The single acute bout of exercise prevented or attenuated some of the anthracycline-induced negative effects on cardiomyocytes including oxidative stress, apoptosis, mitochondrial dysfunction, as well as systolic dysfunction. There are no studies to date that have investigated the cardiac effects of an acute bout of exercise in close proximity to anthracycline infusion in humans. Aerobic exercise training is recommended throughout chemotherapy treatment, but there are no guidelines in place in terms of the timing of exercise in relation to receipt of chemotherapy infusions.

  2. Objectives

  1. To compare the acute effect of performing exercise (within 24 hours before the first infusion) compared to no exercise (no exercise for 72 hours prior to the first infusion) on markers of subclinical cardiotoxicity 24-48 hours after the first anthracycline infusion.
  2. To compare the chronic effect of performing exercise (within 24 hours before every infusion) compared to no exercise (no exercise for 72 hours prior to every infusion) on markers of cardiotoxicity 7 to 14 days after the final anthracycline infusion 5) Research Method This study will be a two-arm randomized control trial. Twenty-four women aged 18 or older newly diagnosed with stage I-IIIA breast cancer, and scheduled to receive neoadjuvant or adjuvant doxorubicin chemotherapy in cycles of 2-3 weeks will be recruited by oncologist referral and posters. Participants will be randomized to one of two conditions: i) an acute bout of exercise performed ≤24 hours prior to each cycle of anthracyclines and no exercise for 48 hours post; or ii) no exercise for 72 hours prior or 48 hours post each cycle of anthracyclines.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •newly diagnosed with stage I-IIIA breast cancer
  • •scheduled to receive neoadjuvant or adjuvant doxorubicin chemotherapy in cycles of 2-3 weeks long
  • •receive their oncologist's approval to exercise
  • •be able to complete first time point of data collection prior to first chemotherapy cycle
  • •be able to understand and provide written informed consent in English

排除标准

  • •concurrent participation in a structured exercise program or study
  • •have orthopedic limitations to exercise
  • •pre-existing cardiovascular disease
  • •uncontrolled hypertension (blood pressure ≥ 140/90 mmHg)
  • •uncontrolled diabetes
  • •respiratory disease
  • •current smoking status

研究组 & 干预措施

Exercise

Experimental

an acute bout of exercise performed ≤24 hours prior to each cycle of anthracyclines and no exercise for 48 hours post

干预措施: exercise (Other)

No exercise

No Intervention

no exercise for 72 hours prior or 48 hours post each cycle of anthracyclines

结局指标

主要结局

Global Longitudinal Strain

时间窗: 24-48 hours after first doxorubicin and 7-14 days after completion of last doxorubicin cycle

Assessed with 2D speckle tracking echocardiography

次要结局

  • Cardiac Troponin T(24-48 hours after first doxorubicin and 7-14 days after completion of last doxorubicin cycle)
  • LV Twist(24-48 hours after first doxorubicin and 7-14 days after completion of last doxorubicin cycle)
  • NT-proBNP(24-48 hours after first doxorubicin and 7-14 days after completion of last doxorubicin cycle)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kristin Campbell

Dr. Kristin Campbell

University of British Columbia

研究点 (1)

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