PASAPAS: Impact of Nutritional Intervention in Women With Breast Cancer Under Adjuvant Chemotherapy

Sponsor
Centre Leon Berard (Other)
Overall Status
Completed
CT.gov ID
NCT01331772
Collaborator
National Cancer Institute, France (Other), Ligue du Rhône (Other), Fondation de France (Other), Cancéropôle Lyon Auvergne Rhône-Alpes (Other), Lions Club Bourg-en-Bresse et Pérouges (Other), Association Lyonnaise de Logistique Posthospitalière (Other), Ministère de la Recherche (Other)
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Study Details

Study Description

Brief Summary

Breast cancer is the most common cancer in women. Weight gain in adulthood, overweight or obesity, physical inactivity and alcohol consumption are risk factors commonly associated with risk of breast cancer (mainly for post-menopausal for overweight and obesity). Reduced physical activity is one factor likely to weight gain in women after adjuvant chemotherapy for localized breast cancer. Furthermore, physical activity appropriately could improve many prognostic factors and survival of women after breast cancer. Adapted Physical Activity (APA) could improve fitness, quality of life, body image, treatment compliance and reduce fatigue.

After diagnosis of breast cancer, there is many possible risk factors of mortality or morbidity related to nutritional factors available to management. These risks prevention through management of these patients appears indispensable through an APA program.

Thus, the investigators propose to test the feasibility of implementing a program of dietary intervention and APA to prevent the risk of weight gain (which affects more than half of patients) and maintain and/or increase their level of physical activity during and after adjuvant chemotherapy.

Condition or Disease Intervention/Treatment Phase
  • Other: Control arm
  • Other: Intervention arm
N/A

Detailed Description

With approximately 52,600 new cases diagnosed in France in 2010, breast cancer is the most common cancer in women, according to national projections of the incidence and cancer mortality for 2010.

Weight gain in adulthood, overweight or obesity, physical inactivity and alcohol consumption are risk factors commonly associated with risk of breast cancer (mainly for post-menopausal for overweight and obesity).

Several hypotheses explain the association between obesity and breast cancer: obesity, metabolic syndrome and diabetes participate to changes in hormone levels (estrogen, leptin, insulin) that promotes mammary carcinogenesis and tumor progression.

The association between obesity and development of breast cancer is partly due to increased serum levels of estradiol produced by adipocytes, but the role of insulin resistance and inflammation associated with obesity is widely discussed.

Reduced physical activity is one factor likely to weight gain in women after adjuvant chemotherapy for localized breast cancer. Furthermore, physical activity appropriately could improve many prognostic factors and survival of women after breast cancer. Thus, several large cohort studies of women with breast cancer showed an average mortality reduction of 45% associated with moderate physical activity compared with inactivity. Adapted Physical Activity (APA) could also improve fitness, quality of life, body image, treatment compliance and reduce fatigue.

A rich fruits and vegetables diet combined with regular physical activity appears to offer the best protection from breast cancer. The nature, frequency, duration, intensity and arrangement of physical training program meetings are key elements to consider, metabolic responses differ according to these factors.

The optimal management for an improved level of physical activity appear to be an individual of at least three sessions per week, 30 to 60 minutes each with a moderate intensity, allowing a physiological response to chronic exercise and an adequate recovery.

After diagnosis of breast cancer, there is thus many possible risk factors of mortality or morbidity related to nutritional factors available to management. These risks prevention through management of these patients appears indispensable through an APA program.

Thus, the investigators propose to test the feasibility of implementing a program of dietary intervention and APA to prevent the risk of weight gain (which affects more than half of patients) and maintain and/or increase their level of physical activity during and after adjuvant chemotherapy.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Official Title:
Randomized Controlled Study Assessing the Feasibility and the Medico-economic Impact of Nutritional Intervention in Women With Breast Cancer Under Adjuvant Chemotherapy
Study Start Date :
Jul 1, 2011
Actual Primary Completion Date :
Jul 1, 2014
Actual Study Completion Date :
Jul 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Other: Control arm

Dietetic follow-up only

Other: Control arm
Dietetic follow-up only

Experimental: Intervention arm

Dietetic + adapted physical activity

Other: Intervention arm
Dietetic follow up + adapted physical activity
Other Names:
  • APA arm
  • Outcome Measures

    Primary Outcome Measures

    1. Assessment in a cohort of adult patients with a 1st breast cancer non-metastatic, the feasibility of implementing an APA intervention during 6 months, in addition to a dietary management, concomitant to prescription of a first-line adjuvant chemotherapy [6 months]

      Proportion of patients who participate in at least two mandatory APA sessions by week during all the APA program, except during the 1st week of each course of CT

    Secondary Outcome Measures

    1. Assessment of patients compliance to the implementation of the APA program and analyze of the reasons for noncompliance [6 months]

      Rate of patients who completed the full program and analysis of non-compliance grounds during the program

    2. Assessment of acceptability of the intervention and randomization / recruiting capabilities [6 months]

      Number of patients contacted by the investigator to participate in the study and rate of patients randomized

    3. Verification of adequacy between the conduct procedures of program (APA and dietetic) and the constraints of program implementing in real conditions [12 months]

      Formalization of a program used in real conditions

    4. Description of patient satisfaction [Month 12]

      Calculation of overall satisfaction score of patients on the treatment received, evaluated by a scale of satisfaction

    5. Medico-economic impact of the intervention [12 months]

      Settlement expenses costs, incurred costs and costs avoided by the intervention

    6. Biological study [Day 1 CT, week 9, week 24, month 12]

      Analyses of metabolomic profiles and adipokines expression linked to breast cancer at initial diagnosis (before surgery) and description of metabolism changes during nutritional interventions and therapeutic care

    7. Description of dietary [Day 1 CT, week 24, month 12]

      Collection of patient nutritional intake during 3 days by self-administered questionnaire

    8. Description of level and pattern physical activity [Day 1 CT, Week 9, Week 24, Month 12]

      Evaluation of level and pattern physical evaluation (PAQAP and IPAQ questionnaire)

    9. Description of anthropometry [Day 1 CT, week 9, week 24, month 12]

      Measurement of weight, height, waist and hip circumference

    10. Description of lipid profiles [Day 1 CT, week 9, week 24, month 12]

      Measurement of total cholesterol, HDL, LDL and triglycerides

    11. Assessment of life quality [Day 1 CT, week 24, month 12]

      Life quality scores calculation (QLQ-C30, BR-23, MOS SF-36)

    12. Description of anxiety [Day 1 CT, week 24, month 12]

      score calculation of anxiety (STAI questionnaire)

    13. Assessment of patients compliance to the implementation of diet and analyze of the reasons for noncompliance [6 months]

      Rate of patients who completed the full program and analysis of non-compliance grounds during the program

    14. Description of body satisfaction [Day 1 CT, week 24, month 12]

      score calculation of QSCPGS questionnaire

    15. Description of body composition [Day 1 CT, week 9, week 24, month 12]

      Measurement of body composition by impedancemetry

    16. Description of self-perception [Day 1 CT, week 24, month 12]

      score calculation of self-perception (QSCPGS questionnaire)

    17. Description of self esteem [Day 1 CT, week 24, month 12]

      score calculation of self-esteem (Rosenzweig scale)

    18. Description of depression [Day 1 CT, week 24, month 12]

      score calculation of depression (BDI questionnaire)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 75 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Female, 18 years ≤ age < 75 years

    • With an invasive, non-metastatic, histologically confirmed, first breast carcinoma

    • Requiring the prescription of a first line of adjuvant chemotherapy

    • Followed in the research center

    • Whose ability to participate in the APA intervention has been certified by a medical certificate issued by physician, the referring physician or the physician investigator

    • Residing within a radius of 60 km around the center investigator or agreeing to bear the travel costs beyond proposed reimbursement

    • Availability and willingness to invest in the PASAPAS study during the program (6 months) and during the post-program follow-up (6 months)

    • Able to understand, read and write French

    • Covered by a medical insurance

    • Written, signed informed consent

    Exclusion Criteria:
    • Female with metastatic or inflammatory breast cancer,

    • History or concomitant primary cancer (except for carcinoma in situ of the uterine cervix and/or skin basal cell carcinoma and or colon carcinoma in situ and/or not a breast cancer in complete response for at least 5 years)

    • Cons-indication to physical activity practice, at discretion of the investigator,

    • In a state of severe malnutrition according to the criteria of the High Authority for

    Health (HAS) 2010, namely:
    • Among women ≤ 70 years: weight loss ≥ 15% in 6 months or ≥ 10% in 1 month

    • Among women > 70 years: weight loss ≥ 15% in 6 months or ≥ 10% in 1 month, body mass index < 18 kg / m²

    • History of eating disorders,

    • Not possible follow-up for medical, social, familial, geographical or psychological reasons, during the program (6 months) and during the post-program follow-up (6 months),

    • Deprived of their liberty by court or administrative decision,

    • Pregnant or nursing, of childbearing age without effective contraception during the study.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Centre Leon Berard Lyon Cedex 08 France 69373

    Sponsors and Collaborators

    • Centre Leon Berard
    • National Cancer Institute, France
    • Ligue du Rhône
    • Fondation de France
    • Cancéropôle Lyon Auvergne Rhône-Alpes
    • Lions Club Bourg-en-Bresse et Pérouges
    • Association Lyonnaise de Logistique Posthospitalière
    • Ministère de la Recherche

    Investigators

    • Principal Investigator: Patrick BACHMANN, MD, Centre Leon Berard

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Centre Leon Berard
    ClinicalTrials.gov Identifier:
    NCT01331772
    Other Study ID Numbers:
    • PASAPAS
    • 2011-A00064-37
    First Posted:
    Apr 8, 2011
    Last Update Posted:
    Oct 30, 2014
    Last Verified:
    Oct 1, 2014
    Keywords provided by Centre Leon Berard
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 30, 2014