Diet Composition, Weight Control, and Breast Carcinogenesis (CHOICE)
Primary Purpose
Breast Cancer
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Weight Loss Dietary Pattern
Sponsored by
About this trial
This is an interventional prevention trial for Breast Cancer focused on measuring Breast cancer, survivors, weight lose, dietary pattern
Eligibility Criteria
Inclusion Criteria:
- Female breast cancer survivors
- Staged, resected breast cancer (> 4-months post radiation treatment, chemotherapy or surgery)
- Post-menopausal (no menses for > 6 months)
- No evidence of metastatic breast disease
- Willing to follow the diet plan prescribed
- Willing to follow the guidelines for alcohol consumption (no more than 1 standard alcoholic drink per day where one serving is defined as 12oz beer, 5 oz wine OR 1 oz hard liquor)
- Willing to maintain or increase current physical activity level
- Willing to wear a pedometer and keep a daily record of steps
- Willing to wear heart rate/ accelerometer device (Actiheart) continuously (24/7) for one week at the start and end of the study
- Willing to wear a body or swim suit and cap for body composition tests
- Willing to record food intake daily
- Willing to come to RMCC Rose for 11 individual and 5 group sessions over a 6 month period
- Willing to provide urine and fasting blood samples at 7 visits during the study
- Willing to make the commitment it takes to lose weight for the study
- Must have a Body Mass Index between 25Kg/m2 to 35Kg/m2.
Exclusion Criteria:
- Anticipates having surgery during the next 6 months
- Follows a special diet, e.g. gluten free, casein free, dairy free, vegetarian or other
- Lost 4 or more pounds during the previous month
- Taking weight loss medications during the study
- Being treated by a physician for diabetes
- Has an eating disorder
- Has digestive problems such as IBS (Irritable Bowel Syndrome), Crohn's or other
- Has had surgery involving constriction or removal of any portion of the gastrointestinal tract (gastric bypass, lap-band, bowel resection, colostomy etc.
- Diagnosed with hepatitis B, hepatitis C or HIV
- Has electronic devices implanted in their body (pacemaker, vagus nerve stimulator)
- Must not use any tobacco products
Sites / Locations
- Rocky Mountain Cancer Center
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
No Intervention
Arm Label
Low fat, high carb weight loss diet
Low carb, high fat weight loss diet
Control
Arm Description
Ornish-like weight loss dietary pattern
South-Beach-like weight loss diet pattern
Usual care
Outcomes
Primary Outcome Measures
Inflammation Markers
C-reactive protein, IL-6, TNF-alpha
Secondary Outcome Measures
Body Fat Percentage (%)
% Body fat, % lean muscle mass, Resting Metabolic Rate (RMR) using the BODPOD (Volumetric weighing; Life Measurement, Inc.) and Tanita Bioelectrical Impedence (BI)
Waist Hip Ratio
Calculated by measuring and dividing waist and hip circumferences
Weight
Using 1) BODPOD (Life Measurement, Inc.) and 2) Tanita Bioelectrical Impedence Scale
Bioavailable sex steroid hormones
estradiol, estrone, sex hormone binding globulin (SHBG)
Glucose metabolism
glucose, insulin, IGF-1, IGFBP-3, glycated proteins (HbA1c)
Cellular oxidation
8-hydroxy-2-deoxyguanosine, DNA damage sensitivity and repair and 8-isoprostane-F-2-alpha
Full Information
NCT ID
NCT01315483
First Posted
March 14, 2011
Last Updated
February 13, 2013
Sponsor
Colorado State University
1. Study Identification
Unique Protocol Identification Number
NCT01315483
Brief Title
Diet Composition, Weight Control, and Breast Carcinogenesis
Acronym
CHOICE
Official Title
Diet Composition, Weight Control, and Breast Carcinogenesis
Study Type
Interventional
2. Study Status
Record Verification Date
February 2013
Overall Recruitment Status
Completed
Study Start Date
September 2008 (undefined)
Primary Completion Date
January 2012 (Actual)
Study Completion Date
June 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Colorado State University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
In the United States, overweight (BMI > 25 but < 30 Kg/m2) and obesity (BMI > 30Kg/m2) are increasing at epidemic rates. A significant association exists between being overweight or obese and breast cancer recurrence and survival. However, evidence continues to accumulate indicating that achieving or maintaining a healthy weight for height (Body Mass Index, BMI, 18.5-25Kg/m2) is associated with a reduced risk for breast cancer and with a decrease in breast cancer associated mortality. Despite this, there is a lack of randomized controlled trials exploring this association and how the process of fat loss or being successful in actually reaching a healthy weight for height differentially affects biomarkers for cancer recurrence.
Many dietary approaches for weight loss are currently available to the public, and each purports to offer advantages. However, there is little scientific evidence to indicate how these dietary approaches, some of which vary markedly in the foods that they limit or exclude, affect biomarkers for breast cancer risk. In particular, it is not know whether the critical factor in relation to weight and breast cancer is simply weight loss (negative energy balance), irrespective of the manner in which it is achieved, or if certain dietary approaches affect breast cancer risk biomarkers more favorably than others. Published data from our laboratory suggest that dietary pattern does matter, and therefore the goal of this study is to investigate the effects of two popular weight loss dietary approaches that differ in the extent to which they limit carbohydrate or fat consumption (with effects on dietary glycemic load) compared to a usual care group on prognostic markers for cancer recurrence in postmenopausal breast cancer survivors. The investigators hypothesize that in addition to the anticipated effects of fat loss on circulating levels of bioavailable sex steroid hormones, that the effects of excess fat on breast cancer prognosis can be attributed to three interrelated metabolic processes that affect cancer progression: altered glucose metabolism, chronic inflammation and excessive cellular oxidation.
Detailed Description
This study is designed to answer questions about how a dietary pattern either high or low in dietary carbohydrate and fat availability and fat loss influence metabolic and hormonal processes that may affect breast cancer recurrence. The investigators hypothesize that in addition to the anticipated effects of fat loss on circulating levels of bioavailable sex steroids, that the effects of excess fat on breast cancer prognosis can be attributed to three interrelated metabolic processes: altered glucose metabolism (IGF-1, IGFBP-3, glycated proteins), chronic inflammation (C-reactive protein, IL-6, TNF-alpha) and excessive cellular oxidation (8-hydroxy-2-deoxyguanosine and 8-isoprostane F-2 alpha).
A 6 month intervention study involving 370 post menopausal women who have been treated for breast cancer is proposed. Randomized women, stratified by resected stage, systemic adjuvant therapy and body mass index (> 25 and < 35 Kg/m2), will serve as either a non-intervention control group or will follow a tailored diet-physical activity program designed to create a weekly negative energy balance equivalent to 3500 kcal. The intervention groups will receive the same physical activity protocol, but one of two diets that differ in dietary pattern.
The specific aims are: Aim 1. Does a dietary pattern either high or low in available carbohydrate and fat alter the pattern of change observed in circulating factors involved in glucose homeostasis, chronic inflammation, cellular oxidation, and steroid hormone metabolism during progressive loss of body fat? The investigators will also examine how observed changes in these circulating factors related to changes indicators of breast cancer recurrence. Aim 2. Do circulating factors associated with glucose homeostasis, chronic inflammation, and cellular oxidation display the same pattern of change in response to progressive fat loss as circulating analytes associated with sex steroid metabolism? Analytes of interest will be measured monthly throughout the study. Aim 3. Does dietary glycemic load affect the magnitude or rate of fat loss? Plasma adipokines such as leptin and adiponectin and plasma ghrelin will be measured to provide biological determinants that may help explain differences in response.
The work proposed in this application should provide quantitative data about the importance of the magnitude of fat loss on metabolic and hormonal processes involved in cancer recurrence and provide guidance about effective dietary approaches that maximize weight loss benefits on breast cancer prognosis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
Breast cancer, survivors, weight lose, dietary pattern
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
259 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Low fat, high carb weight loss diet
Arm Type
Experimental
Arm Description
Ornish-like weight loss dietary pattern
Arm Title
Low carb, high fat weight loss diet
Arm Type
Experimental
Arm Description
South-Beach-like weight loss diet pattern
Arm Title
Control
Arm Type
No Intervention
Arm Description
Usual care
Intervention Type
Other
Intervention Name(s)
Weight Loss Dietary Pattern
Other Intervention Name(s)
Low fat, high carb weight loss diet (Vivace Diet), Low carb, high fat weight loss diet (Ricca Diet)
Intervention Description
Diet-physical activity program creating a weekly negative energy balance equivalent to 3500 kcal. Intervention groups receive PA protocol promoting the Physical Activity Guidelines and translated in step recommendations, but one of two diets with divergent dietary patterns (opposing fat and CHO content) that do not overlap >+5% in CHO and fat content. Macronutrient values reflect a 'pattern' or ratio within (LC 3:2 ratio for F:CHO; HC 1:4 ratio for F:CHO ) and between diets (LC:HC 3:1 for fat; LC:HC 1:2 for CHO). Six-week meal plans for five calorie levels available and incorporate educational material, supporting program components (e.g. self monitoring tools) and core competencies reinforcing weight loss behaviors in order to promote high levels of dietary adherence.
Primary Outcome Measure Information:
Title
Inflammation Markers
Description
C-reactive protein, IL-6, TNF-alpha
Time Frame
Baseline and montlhly for 6 months
Secondary Outcome Measure Information:
Title
Body Fat Percentage (%)
Description
% Body fat, % lean muscle mass, Resting Metabolic Rate (RMR) using the BODPOD (Volumetric weighing; Life Measurement, Inc.) and Tanita Bioelectrical Impedence (BI)
Time Frame
Baseline and monthly for 6 months
Title
Waist Hip Ratio
Description
Calculated by measuring and dividing waist and hip circumferences
Time Frame
Baseline and monthly for 6 months
Title
Weight
Description
Using 1) BODPOD (Life Measurement, Inc.) and 2) Tanita Bioelectrical Impedence Scale
Time Frame
Baseline and monthly for 6 months
Title
Bioavailable sex steroid hormones
Description
estradiol, estrone, sex hormone binding globulin (SHBG)
Time Frame
Baseline and monthly for 6 months
Title
Glucose metabolism
Description
glucose, insulin, IGF-1, IGFBP-3, glycated proteins (HbA1c)
Time Frame
Baseline and monthly for 6 months
Title
Cellular oxidation
Description
8-hydroxy-2-deoxyguanosine, DNA damage sensitivity and repair and 8-isoprostane-F-2-alpha
Time Frame
Baseline and monthly for 6 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Female breast cancer survivors
Staged, resected breast cancer (> 4-months post radiation treatment, chemotherapy or surgery)
Post-menopausal (no menses for > 6 months)
No evidence of metastatic breast disease
Willing to follow the diet plan prescribed
Willing to follow the guidelines for alcohol consumption (no more than 1 standard alcoholic drink per day where one serving is defined as 12oz beer, 5 oz wine OR 1 oz hard liquor)
Willing to maintain or increase current physical activity level
Willing to wear a pedometer and keep a daily record of steps
Willing to wear heart rate/ accelerometer device (Actiheart) continuously (24/7) for one week at the start and end of the study
Willing to wear a body or swim suit and cap for body composition tests
Willing to record food intake daily
Willing to come to RMCC Rose for 11 individual and 5 group sessions over a 6 month period
Willing to provide urine and fasting blood samples at 7 visits during the study
Willing to make the commitment it takes to lose weight for the study
Must have a Body Mass Index between 25Kg/m2 to 35Kg/m2.
Exclusion Criteria:
Anticipates having surgery during the next 6 months
Follows a special diet, e.g. gluten free, casein free, dairy free, vegetarian or other
Lost 4 or more pounds during the previous month
Taking weight loss medications during the study
Being treated by a physician for diabetes
Has an eating disorder
Has digestive problems such as IBS (Irritable Bowel Syndrome), Crohn's or other
Has had surgery involving constriction or removal of any portion of the gastrointestinal tract (gastric bypass, lap-band, bowel resection, colostomy etc.
Diagnosed with hepatitis B, hepatitis C or HIV
Has electronic devices implanted in their body (pacemaker, vagus nerve stimulator)
Must not use any tobacco products
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Henry J Thompson, PhD
Organizational Affiliation
Colorado State University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Scot M Sedlacek, MD
Organizational Affiliation
Rocky Mountain Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rocky Mountain Cancer Center
City
Denver
State/Province
Colorado
ZIP/Postal Code
80220
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
26010254
Citation
Thompson HJ, Sedlacek SM, Playdon MC, Wolfe P, McGinley JN, Paul D, Lakoski SG. Weight loss interventions for breast cancer survivors: impact of dietary pattern. PLoS One. 2015 May 26;10(5):e0127366. doi: 10.1371/journal.pone.0127366. eCollection 2015.
Results Reference
derived
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Diet Composition, Weight Control, and Breast Carcinogenesis
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