Exercise to Prevent Aromatase Inhibitor Side Effects in Breast Cancer Patients (BCS2)
Primary Purpose
Breast Cancer, Sarcopenia
Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Structured Exercise
Usual Care
Sponsored by
About this trial
This is an interventional prevention trial for Breast Cancer
Eligibility Criteria
Inclusion Criteria:
- At least mild fatigue in 2 of the 4 areas of the Piper Fatigue Scale (score ≥ 1-3)
- Completion of standard surgery +/- chemotherapy for breast cancer (may undergo radiation therapy during study)
- 25-OH vitamin D > 20 ng/ml
- Histological evidence of stage I-III hormone receptor-positive breast cancer
- Body Mass Index >/=18 and <50 kg/m2
- 40-80 years of age
- Non-smoking (non smoking for at least 12 months: cigarettes, cigars, pipes
- Menopause over one year (absence of menses for 12 months or greater)
- Sedentary (exercise no >60 min 2 times/week)
Exclusion Criteria:
- Taking oral steroids, warfarin, or other medications interfering with fat metabolism that may not be safely discontinued temporarily for specific produces (i.e. for 72 hours prior)
- Symptomatic heart disease, coronary artery disease, congestive heart failure, or uncontrolled hypertension (systolic blood pressure over 180 mm HG)unless medically stabilized
- Participant is, in the opinion of the investigator, unable to adhere to the study protocol due to medical or orthopedic conditions that limit ability to exercise or travel to the Baltimore VA for protocol procedures
- Chronic pulmonary disease (on supplemental O2)
- Abnormal renal function (BUN above 40 mg/dl, Cr above 1.3 mg/dl, CrCl<60mg/dl)
- Unstable lymphedema
- Evidence of cancer metastases or recurrence
- Anemia HCT below 30 mg/dl, platelets below 80,000/cm3
- Type 1 diabetes; insulin treatment for diabetes, poorly controlled diabetes, HgA1c>10%
- Abnormal response to exercise test (ST segment depression greater than 2mm, chest pain, significant arrhythmias, extreme shortness of breath, cyanosis, exercising BP above 240/120 mm HG, or other contraindications to exercise) confirmed with further diagnostic evaluations.
- Abnormal liver function
- Untreated dyslipidemia with National Cholesterol ATPIII 10 year cardiac risk score greater than 10% (www.nhlbi.nih.gov/guidelines/cholesterol/atp3upd04.htm)
- Metal implants or devices (i.e. pacemaker) if undergoing CT scan
- History of seizures or taking anti-seizure or anti convulsion medication
- Allergic to lidocaine
- Mini-mental state examination below 24, dementia, or unstable clinical depression by exam
Sites / Locations
- Baltimore VA Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Structured Exercise
Usual Care
Arm Description
Structured and supervised aerobic and resistance training 2 times per week
Subjects will be counseled on American Cancer Society and American College of Sports Medicine physical activity and nutritional guidelines at the initiation of the study. Study participants will be contacted by a physician or nurse on weeks 2, 6, 10, and 14 to provide support and encouragement to patients.
Outcomes
Primary Outcome Measures
Fatigue
Fatigue (questionnaires) and muscle performance (muscle strength, endurance, and function)
Muscle performance (muscle strength, endurance, and function) Fatigue and Muscle Performance
Fatigue (questionnaire) and muscle performance (muscle strength, endurance, and function)
Musculoskeletal symptoms (VASpain, HAQ-DI)
Musculoskeletal symptoms (VASpain, HAQ-DI)
Secondary Outcome Measures
Glucose Tolerance and Inflammation
Glucose Tolerance and Inflammation
Full Information
NCT ID
NCT01954706
First Posted
September 27, 2013
Last Updated
November 25, 2015
Sponsor
Baltimore VA Medical Center
Collaborators
National Institute on Aging (NIA)
1. Study Identification
Unique Protocol Identification Number
NCT01954706
Brief Title
Exercise to Prevent Aromatase Inhibitor Side Effects in Breast Cancer Patients
Acronym
BCS2
Official Title
Pilot Trial of Aerobic and Resistance Exercise Training for the Primary Prevention of Musculoskeletal Side Effects From Aromatase Inhibitors in Postmenopausal Breast Cancer Patients
Study Type
Interventional
2. Study Status
Record Verification Date
November 2015
Overall Recruitment Status
Terminated
Why Stopped
The study was stopped due to recruitment difficulties
Study Start Date
November 2013 (undefined)
Primary Completion Date
September 2015 (Actual)
Study Completion Date
September 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Baltimore VA Medical Center
Collaborators
National Institute on Aging (NIA)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Hormone receptor-positive tumors are the most common breast cancers in postmenopausal women, and drug therapies, which block the production or effects of estrogen, are the mainstay of treatment in these patients. Due to their effectiveness in postmenopausal women, aromatase inhibitors (AIs) are the standard of care for long-term estrogen suppression in these patients. Estrogen deficiency, however, results in multiple side effects. Some of the most common side effects in women taking AIs are joint and muscle aches, which promote physical deconditioning. Because of the long term use of AIs in postmenopausal breast cancer patients and the improvements in cancer-related outcomes that are observed with their use, identifying methods to reduce these side effects to maintain adherence to treatment is important. Exercise interventions in breast cancer patients also improve quality of life and reduce fatigue. Understanding the role of exercise in AI side effect prevention will allow us to translate these findings into therapy guidelines.
Detailed Description
Breast cancer is the most common malignancy in women in the United States and is the second leading cause of cancer deaths. In 2013, an estimated 230,000 women in the United States will be diagnosed with invasive breast cancer and approximately 40,000 with die.1 Women with breast cancer frequently experience significant functional and metabolic declines during and after treatment due to cancer-related fatigue (CRF), stress and depression.2,3 Cancer-related fatigue is associated with side effects from treatment, pain, functional disability, sleep disturbances, mood disturbances and co-morbid conditions.4 Patients with CRF have declines in physical activity and function, which significantly impacts quality of life (QOL).5 The mechanisms underlying functional declines and fatigue in breast cancer patients are likely multifactorial, but deconditioning, sarcopenia, increases in inflammatory cytokines, insulin resistance, and changes in muscle and fat metabolism seem to play important roles.4,6
Hormone receptor-positive tumors are the most common breast cancers in postmenopausal women, and endocrine therapies, which block the production or effects of estrogen, are the mainstay of treatment in these patients. Due to their superior efficacy in postmenopausal women, aromatase inhibitors (AIs) are the standard of care for long-term estrogen suppression in these patients.7 Estrogen deprivation, however, results in multiple side effects which may worsen fatigue and the functional and metabolic declines associated with cancer treatment.8 Some of the most common side effects in women taking AIs are musculoskeletal symptoms, including arthralgias and myalgias, which promote deconditioning and sarcopenia and their associated side effects.9 Because of the prolonged use of AIs in postmenopausal breast cancer patients and the improvements in cancer-related outcomes that are observed with their use, great efforts are taken to reduce AI induced musculoskeletal symptoms (AIMSS) to maintain adherence to treatment. While multiple strategies are used to manage AIMSS, current therapies mainly focus on interventions in patients who develop symptoms (tertiary prevention) rather than primary prevention.9 Exercise interventions in breast cancer patients also improve QOL, decrease fatigue, and increase physical function and strength.10,11 Understanding the role of exercise in AI side effect prevention will allow us to translate these findings into therapy guidelines.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Sarcopenia
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
5 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Structured Exercise
Arm Type
Experimental
Arm Description
Structured and supervised aerobic and resistance training 2 times per week
Arm Title
Usual Care
Arm Type
Active Comparator
Arm Description
Subjects will be counseled on American Cancer Society and American College of Sports Medicine physical activity and nutritional guidelines at the initiation of the study. Study participants will be contacted by a physician or nurse on weeks 2, 6, 10, and 14 to provide support and encouragement to patients.
Intervention Type
Other
Intervention Name(s)
Structured Exercise
Intervention Description
Structured and supervised aerobic and resistance training 2 times per week
Intervention Type
Other
Intervention Name(s)
Usual Care
Intervention Description
Subjects will be counseled on American Cancer Society and American College of Sports Medicine physical activity and nutritional guidelines at the initiation of the study. Study participants will be contacted by a physician or nurse on weeks 2, 6, 10, and 14 to provide support and encouragement to patients.
Primary Outcome Measure Information:
Title
Fatigue
Description
Fatigue (questionnaires) and muscle performance (muscle strength, endurance, and function)
Time Frame
Baseline
Title
Muscle performance (muscle strength, endurance, and function) Fatigue and Muscle Performance
Description
Fatigue (questionnaire) and muscle performance (muscle strength, endurance, and function)
Time Frame
16 weeks
Title
Musculoskeletal symptoms (VASpain, HAQ-DI)
Description
Musculoskeletal symptoms (VASpain, HAQ-DI)
Time Frame
16 weeks
Secondary Outcome Measure Information:
Title
Glucose Tolerance and Inflammation
Time Frame
Baseline
Title
Glucose Tolerance and Inflammation
Time Frame
16 weeks
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
At least mild fatigue in 2 of the 4 areas of the Piper Fatigue Scale (score ≥ 1-3)
Completion of standard surgery +/- chemotherapy for breast cancer (may undergo radiation therapy during study)
25-OH vitamin D > 20 ng/ml
Histological evidence of stage I-III hormone receptor-positive breast cancer
Body Mass Index >/=18 and <50 kg/m2
40-80 years of age
Non-smoking (non smoking for at least 12 months: cigarettes, cigars, pipes
Menopause over one year (absence of menses for 12 months or greater)
Sedentary (exercise no >60 min 2 times/week)
Exclusion Criteria:
Taking oral steroids, warfarin, or other medications interfering with fat metabolism that may not be safely discontinued temporarily for specific produces (i.e. for 72 hours prior)
Symptomatic heart disease, coronary artery disease, congestive heart failure, or uncontrolled hypertension (systolic blood pressure over 180 mm HG)unless medically stabilized
Participant is, in the opinion of the investigator, unable to adhere to the study protocol due to medical or orthopedic conditions that limit ability to exercise or travel to the Baltimore VA for protocol procedures
Chronic pulmonary disease (on supplemental O2)
Abnormal renal function (BUN above 40 mg/dl, Cr above 1.3 mg/dl, CrCl<60mg/dl)
Unstable lymphedema
Evidence of cancer metastases or recurrence
Anemia HCT below 30 mg/dl, platelets below 80,000/cm3
Type 1 diabetes; insulin treatment for diabetes, poorly controlled diabetes, HgA1c>10%
Abnormal response to exercise test (ST segment depression greater than 2mm, chest pain, significant arrhythmias, extreme shortness of breath, cyanosis, exercising BP above 240/120 mm HG, or other contraindications to exercise) confirmed with further diagnostic evaluations.
Abnormal liver function
Untreated dyslipidemia with National Cholesterol ATPIII 10 year cardiac risk score greater than 10% (www.nhlbi.nih.gov/guidelines/cholesterol/atp3upd04.htm)
Metal implants or devices (i.e. pacemaker) if undergoing CT scan
History of seizures or taking anti-seizure or anti convulsion medication
Allergic to lidocaine
Mini-mental state examination below 24, dementia, or unstable clinical depression by exam
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Susan Kesmodel, MD
Organizational Affiliation
Baltimore VAMC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Baltimore VA Medical Center
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21201
Country
United States
12. IPD Sharing Statement
Citations:
Citation
Society AC. Cancer Facts & Figures 2013. Atlanta: American Cancer Society 2013.
Results Reference
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PubMed Identifier
20044868
Citation
Thomson CA, Thompson PA, Wright-Bea J, Nardi E, Frey GR, Stopeck A. Metabolic syndrome and elevated C-reactive protein in breast cancer survivors on adjuvant hormone therapy. J Womens Health (Larchmt). 2009 Dec;18(12):2041-7. doi: 10.1089/jwh.2009.1365.
Results Reference
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PubMed Identifier
11068951
Citation
Curt GA. Impact of fatigue on quality of life in oncology patients. Semin Hematol. 2000 Oct;37(4 Suppl 6):14-7. doi: 10.1016/s0037-1963(00)90063-5.
Results Reference
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PubMed Identifier
18425939
Citation
Cramp F, Daniel J. Exercise for the management of cancer-related fatigue in adults. Cochrane Database Syst Rev. 2008 Apr 16;(2):CD006145. doi: 10.1002/14651858.CD006145.pub2.
Results Reference
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PubMed Identifier
20861456
Citation
Braithwaite D, Satariano WA, Sternfeld B, Hiatt RA, Ganz PA, Kerlikowske K, Moore DH, Slattery ML, Tammemagi M, Castillo A, Melisko M, Esserman L, Weltzien EK, Caan BJ. Long-term prognostic role of functional limitations among women with breast cancer. J Natl Cancer Inst. 2010 Oct 6;102(19):1468-77. doi: 10.1093/jnci/djq344. Epub 2010 Sep 22.
Results Reference
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PubMed Identifier
22488700
Citation
Berger AM, Gerber LH, Mayer DK. Cancer-related fatigue: implications for breast cancer survivors. Cancer. 2012 Apr 15;118(8 Suppl):2261-9. doi: 10.1002/cncr.27475.
Results Reference
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PubMed Identifier
16675568
Citation
Collado-Hidalgo A, Bower JE, Ganz PA, Cole SW, Irwin MR. Inflammatory biomarkers for persistent fatigue in breast cancer survivors. Clin Cancer Res. 2006 May 1;12(9):2759-66. doi: 10.1158/1078-0432.CCR-05-2398.
Results Reference
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PubMed Identifier
18258989
Citation
Lin NU, Winer EP. Advances in adjuvant endocrine therapy for postmenopausal women. J Clin Oncol. 2008 Feb 10;26(5):798-805. doi: 10.1200/JCO.2007.15.0946.
Results Reference
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PubMed Identifier
21249443
Citation
Dent SF, Gaspo R, Kissner M, Pritchard KI. Aromatase inhibitor therapy: toxicities and management strategies in the treatment of postmenopausal women with hormone-sensitive early breast cancer. Breast Cancer Res Treat. 2011 Apr;126(2):295-310. doi: 10.1007/s10549-011-1351-3. Epub 2011 Jan 20.
Results Reference
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PubMed Identifier
21457526
Citation
Gaillard S, Stearns V. Aromatase inhibitor-associated bone and musculoskeletal effects: new evidence defining etiology and strategies for management. Breast Cancer Res. 2011 Mar 14;13(2):205. doi: 10.1186/bcr2818.
Results Reference
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PubMed Identifier
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Citation
Winters-Stone KM, Dobek J, Bennett JA, Nail LM, Leo MC, Schwartz A. The effect of resistance training on muscle strength and physical function in older, postmenopausal breast cancer survivors: a randomized controlled trial. J Cancer Surviv. 2012 Jun;6(2):189-99. doi: 10.1007/s11764-011-0210-x. Epub 2011 Dec 23.
Results Reference
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Exercise to Prevent Aromatase Inhibitor Side Effects in Breast Cancer Patients
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