Exercise to Prevent AnthrCycline-based Cardio-Toxicity Study (EXACT)
Primary Purpose
Neoplasms, Heart; Disease, Functional, Inflammation
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Moderate Intensity Exercise
Sponsored by
About this trial
This is an interventional treatment trial for Neoplasms focused on measuring Exercise, Quality of Life, Complementary Therapies, Neoadjuvant Therapy, Feasibility Studies
Eligibility Criteria
Inclusion Criteria - Only those patients who meet the following inclusion will be asked to participate in the study:
- Between the ages of 18 and 65;
- Receiving anthracycline chemotherapeutic treatment for a primary/non-recurrent breast or hematological malignancy;
- Are scheduled to received a minimum dose of 100 mg/m2 of doxorubicin (DOX) or 120 mg/m2 of daunorubicin (DAUN), or 150 mg/m2 epirubicin (EPI)
- Within eight weeks of first anthracycline dose;
- Do not have a previous history of myocardial infarction, cerebrovascular disease, peripheral vascular disease, congestive heart failure, or cardiomyopathy (controlled hypertension is not exclusionary);
- Have no known contraindications to light-to-moderate exercise;
- Have no known contraindications to cardiopulmonary exercise stress testing;
- Able to participate in the 12-week community-based exercise program;
- Provided medical consent from their treating physician
Exclusion Criteria:
- Any patients who meet the inclusion criteria, but have any significant cognitive limitations will be excluded from the study.
Sites / Locations
- QEII Health Science Center, Nova Scotia Health Authority
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Moderate Intensity Exercise
Arm Description
All consenting patients will participate in an aerobic training program, twice-weekly over a 12-week period. Assessments will be performed at baseline (pre-training) and post-program (12-weeks). All participants will continue to receive standard care for their cancer diagnosis.
Outcomes
Primary Outcome Measures
Feasibility as measured by rate of recruitment
The rate of recruitment will be measured by comparing the number of patients screened to the number of patients enrolled (patients per month).
Number of adverse events
The number of adverse events associated with exercise program will be used to examine safety.
Secondary Outcome Measures
Feasibility as measured by program adherence
The program adherence will be calculated by dividing the total number of exercise sessions by the number of actual session attended.
Feasibility as measured by attrition rate
The attrition rate will be measured by the number of patients who drop out of the study.
Cardiac Function
Cardiac function will be measured by examining heart chamber size, ventricular function and blood flow between the cardiac chambers using a Multigated acquisition (MUGA) scan.
Cardiac Disease Risk
Cardiac disease risk will be measured using the Framingham Risk Score.
Aerobic Fitness
Aerobic fitness will be measured by comparing baseline and 12 week cardiac stress tests and the associated peak oxygen uptake values.
Fatigue
The Functional Assessment of Cancer Therapy - Fatigue questionnaire will be used to compare baseline and 12 week self-reported levels of fatigue.
Physical Activity Behaviours
Baseline and 12 week levels of physical activity will be measured using the International Physical Activity Questionnaire.
Life Quality
The Functional Assessment of Cancer Therapy - General questionnaire along with the appropriate tumor specific appendix, will be used to compare baseline and 12 week quality of life measures.
Lipid Profile
Baseline and 12 week levels will be compared.
Fasting Glucose
Baseline and 12 week levels will be compared.
High-sensitivity Troponin (hs-TNT)
Baseline and 12 week levels will be compared.
N-terminal of the prohormone brain natriuretic peptide (NTproBNP)
Baseline and 12 week levels will be compared.
C-reactive protein (CRP)
Baseline and 12 week levels will be compared.
Cytokines (IL-1α)
Baseline and 12 week levels (picogram per milileter) will be compared.
Cytokines (IL-1β)
Baseline and 12 week levels (picogram per milileter) will be compared.
Cytokines (IL-4)
Baseline and 12 week levels (picogram per milileter) will be compared.
Cytokines (IL-6)
Baseline and 12 week levels (picogram per milileter) will be compared.
Cytokines (IL-10)
Baseline and 12 week levels (picogram per milileter) will be compared.
Cytokines (IL-17)
Baseline and 12 week levels (picogram per milileter) will be compared.
Cytokines (TNFα)
Baseline and 12 week levels (picogram per milileter) will be compared.
Full Information
NCT ID
NCT02471053
First Posted
May 11, 2015
Last Updated
December 2, 2022
Sponsor
Nova Scotia Health Authority
1. Study Identification
Unique Protocol Identification Number
NCT02471053
Brief Title
Exercise to Prevent AnthrCycline-based Cardio-Toxicity Study
Acronym
EXACT
Official Title
Exercise to Prevent AnthrCycline-based Cardio-Toxicity Study (EXACT)
Study Type
Interventional
2. Study Status
Record Verification Date
December 2022
Overall Recruitment Status
Completed
Study Start Date
February 2016 (undefined)
Primary Completion Date
September 2017 (Actual)
Study Completion Date
September 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nova Scotia Health Authority
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
As the numbers of cancer survivors grow, the long-term adverse effects of cancer therapy are becoming increasingly apparent. Most prominent are the toxic effects on the heart (cardiotoxicity) which may lead to cardiac dysfunction and increased risk of cardiovascular disease (CVD). The investigators hypothesize that an individualized aerobic training program for cancer patients receiving active treatment will be both feasible and safe and will result in improvements in overall levels of physical activity and quality of life.
Feasibility will be assessed by evaluating the recruitment, adherence and attrition rates, along with program safety. Efficacy will be assessed by evaluating changes in health-related outcomes.
Detailed Description
As the numbers of cancer survivors grow, the long-term adverse effects of cancer therapy are becoming increasingly apparent. Most prominent are the toxic effects on the heart (cardiotoxicity) which may lead to cardiac dysfunction and increased risk of cardiovascular disease (CVD). Of note, data indicate that the magnitude of CVD risk for long-term survivors may exceed the risk of a secondary malignancy, which is a known complication of primary cancer therapy. While long-term follow-up data in adult cancer survivors is lacking, study of adult survivors of childhood cancers shows that these individuals are 15 times more likely to develop congestive heart failure (CHF), 10 times more likely to develop CVD, and 9 times more likely to suffer a stroke compared individuals who have not had cancer. Thus, it is clear that the long-term cardiotoxic effects of cancer therapy represent a significant concern for cancer survivors. The mechanisms responsible for the damaging effects of cancer therapy are not fully understood, however there is a need to maximize the benefits of treatment while minimizing long-term damage. Recent animal studies suggest that aerobic exercise training may offer a protective effect against chemotherapy-induced heart disease. However, to the investigator's knowledge, no study to date has examined the potential cardioprotective benefits of exercise training for patients receiving cancer treatment.
Accordingly, the purpose of this pilot study is to evaluate the feasibility and efficacy of a 12-week supervised exercise program based on the principles of cardiac rehabilitation for patients receiving anthracycline-based chemotherapy.
Feasibility will be assessed by evaluating three outcomes, recruitment rate, adherence rate (i.e. exercise class attendance records), attrition rate, and safety (i.e. number of adverse events).
Efficacy will be assessed by evaluating changes in health-related outcomes to assess if these changes are equal to or better than what was measured at baseline. The health-related outcomes include cardiac function and biological markers of cardiotoxicity.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neoplasms, Heart; Disease, Functional, Inflammation
Keywords
Exercise, Quality of Life, Complementary Therapies, Neoadjuvant Therapy, Feasibility Studies
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Moderate Intensity Exercise
Arm Type
Experimental
Arm Description
All consenting patients will participate in an aerobic training program, twice-weekly over a 12-week period. Assessments will be performed at baseline (pre-training) and post-program (12-weeks). All participants will continue to receive standard care for their cancer diagnosis.
Intervention Type
Other
Intervention Name(s)
Moderate Intensity Exercise
Intervention Description
Exercise sessions will be held twice-weekly and will begin with a group warm-up activity, followed by 45 minutes of aerobic activity and ending with a cool down. All aerobic exercise will be performed at a moderate intensity, defined as exercise that elicits a heart rate (HR) between 40-60% of heart rate reserve (HRR). Prior to the initial exercise session target heart rates will be calculated for each subject based on the maximum HR achieved during their baseline stress test.
Primary Outcome Measure Information:
Title
Feasibility as measured by rate of recruitment
Description
The rate of recruitment will be measured by comparing the number of patients screened to the number of patients enrolled (patients per month).
Time Frame
12 Weeks
Title
Number of adverse events
Description
The number of adverse events associated with exercise program will be used to examine safety.
Time Frame
12 Weeks
Secondary Outcome Measure Information:
Title
Feasibility as measured by program adherence
Description
The program adherence will be calculated by dividing the total number of exercise sessions by the number of actual session attended.
Time Frame
12 Weeks
Title
Feasibility as measured by attrition rate
Description
The attrition rate will be measured by the number of patients who drop out of the study.
Time Frame
12 Weeks
Title
Cardiac Function
Description
Cardiac function will be measured by examining heart chamber size, ventricular function and blood flow between the cardiac chambers using a Multigated acquisition (MUGA) scan.
Time Frame
12 Weeks
Title
Cardiac Disease Risk
Description
Cardiac disease risk will be measured using the Framingham Risk Score.
Time Frame
12 Weeks
Title
Aerobic Fitness
Description
Aerobic fitness will be measured by comparing baseline and 12 week cardiac stress tests and the associated peak oxygen uptake values.
Time Frame
12 Weeks
Title
Fatigue
Description
The Functional Assessment of Cancer Therapy - Fatigue questionnaire will be used to compare baseline and 12 week self-reported levels of fatigue.
Time Frame
12 Weeks
Title
Physical Activity Behaviours
Description
Baseline and 12 week levels of physical activity will be measured using the International Physical Activity Questionnaire.
Time Frame
12 Weeks
Title
Life Quality
Description
The Functional Assessment of Cancer Therapy - General questionnaire along with the appropriate tumor specific appendix, will be used to compare baseline and 12 week quality of life measures.
Time Frame
12 Weeks
Title
Lipid Profile
Description
Baseline and 12 week levels will be compared.
Time Frame
12 Weeks
Title
Fasting Glucose
Description
Baseline and 12 week levels will be compared.
Time Frame
12 Weeks
Title
High-sensitivity Troponin (hs-TNT)
Description
Baseline and 12 week levels will be compared.
Time Frame
12 Weeks
Title
N-terminal of the prohormone brain natriuretic peptide (NTproBNP)
Description
Baseline and 12 week levels will be compared.
Time Frame
12 Weeks
Title
C-reactive protein (CRP)
Description
Baseline and 12 week levels will be compared.
Time Frame
12 Weeks
Title
Cytokines (IL-1α)
Description
Baseline and 12 week levels (picogram per milileter) will be compared.
Time Frame
12 Weeks
Title
Cytokines (IL-1β)
Description
Baseline and 12 week levels (picogram per milileter) will be compared.
Time Frame
12 Weeks
Title
Cytokines (IL-4)
Description
Baseline and 12 week levels (picogram per milileter) will be compared.
Time Frame
12 Weeks
Title
Cytokines (IL-6)
Description
Baseline and 12 week levels (picogram per milileter) will be compared.
Time Frame
12 Weeks
Title
Cytokines (IL-10)
Description
Baseline and 12 week levels (picogram per milileter) will be compared.
Time Frame
12 Weeks
Title
Cytokines (IL-17)
Description
Baseline and 12 week levels (picogram per milileter) will be compared.
Time Frame
12 Weeks
Title
Cytokines (TNFα)
Description
Baseline and 12 week levels (picogram per milileter) will be compared.
Time Frame
12 Weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria - Only those patients who meet the following inclusion will be asked to participate in the study:
Between the ages of 18 and 65;
Receiving anthracycline chemotherapeutic treatment for a primary/non-recurrent breast or hematological malignancy;
Are scheduled to received a minimum dose of 100 mg/m2 of doxorubicin (DOX) or 120 mg/m2 of daunorubicin (DAUN), or 150 mg/m2 epirubicin (EPI)
Within eight weeks of first anthracycline dose;
Do not have a previous history of myocardial infarction, cerebrovascular disease, peripheral vascular disease, congestive heart failure, or cardiomyopathy (controlled hypertension is not exclusionary);
Have no known contraindications to light-to-moderate exercise;
Have no known contraindications to cardiopulmonary exercise stress testing;
Able to participate in the 12-week community-based exercise program;
Provided medical consent from their treating physician
Exclusion Criteria:
Any patients who meet the inclusion criteria, but have any significant cognitive limitations will be excluded from the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Scott Grandy, PhD
Organizational Affiliation
Assistant Professor, Affiliate Scientist, Division of Cardiology, Nova Scotia Health Authority
Official's Role
Principal Investigator
Facility Information:
Facility Name
QEII Health Science Center, Nova Scotia Health Authority
City
Halifax
State/Province
Nova Scotia
ZIP/Postal Code
B3H 3A7
Country
Canada
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
20007921
Citation
Albini A, Pennesi G, Donatelli F, Cammarota R, De Flora S, Noonan DM. Cardiotoxicity of anticancer drugs: the need for cardio-oncology and cardio-oncological prevention. J Natl Cancer Inst. 2010 Jan 6;102(1):14-25. doi: 10.1093/jnci/djp440. Epub 2009 Dec 10.
Results Reference
background
PubMed Identifier
16409162
Citation
Yeh ET. Cardiotoxicity induced by chemotherapy and antibody therapy. Annu Rev Med. 2006;57:485-98. doi: 10.1146/annurev.med.57.121304.131240.
Results Reference
background
PubMed Identifier
17035650
Citation
Oeffinger KC, Mertens AC, Sklar CA, Kawashima T, Hudson MM, Meadows AT, Friedman DL, Marina N, Hobbie W, Kadan-Lottick NS, Schwartz CL, Leisenring W, Robison LL; Childhood Cancer Survivor Study. Chronic health conditions in adult survivors of childhood cancer. N Engl J Med. 2006 Oct 12;355(15):1572-82. doi: 10.1056/NEJMsa060185.
Results Reference
background
PubMed Identifier
27965861
Citation
Keats MR, Grandy SA, Giacomantonio N, MacDonald D, Rajda M, Younis T. EXercise to prevent AnthrCycline-based Cardio-Toxicity (EXACT) in individuals with breast or hematological cancers: a feasibility study protocol. Pilot Feasibility Stud. 2016 Aug 5;2:44. doi: 10.1186/s40814-016-0084-9. eCollection 2016.
Results Reference
derived
Learn more about this trial
Exercise to Prevent AnthrCycline-based Cardio-Toxicity Study
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