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Breast Cancer Diet Intervention Study (BCDIS)

Primary Purpose

Early-stage Breast Cancer, Carbohydrate Engorgement, Proliferation

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
PreOP
Sponsored by
Helse Stavanger HF
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Early-stage Breast Cancer focused on measuring Breast Cancer, Estrogen receptor positive, Proliferation, Insulin resistance, PROMs, NMRI, RFS, BCSS

Eligibility Criteria

25 Years - 100 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • All consecutive operable patients in 2009-2010, with a clinical and/or radiologic and/or cytologic diagnosis of primary breast cancer, unless the exclusion criteria apply.

Exclusion Criteria:

  1. Non-operable patients (i.e" patients with T3-4 (>5 cm) disease or distant metastases at the time of operation).
  2. All patients who refuse to participate.
  3. All patients with DCIS, micro-invasive cancer < 2mm diameter or tumors with histologic poor-quality material.
  4. Co-morbidity (Insulin dependent Diabetes Mellitus, Cushing syndrome, previous or concurrent cancers except CIN and non-melanomatous skin cancer.
  5. Mental inability to participate.
  6. Persons allergic to one of the compounds in any of the two diets.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Carbohydrate/intervention group

    Control group

    Arm Description

    Breast cancer patients receive 2 x preoperative carbohydrate loading [PreOP(TM)] before surgery; the 1st dose 18 hours before and 2nd dose 2-4 hours before surgery.

    Breast cancer patients receive standard prep fasting procedure with nil food per os 8-10 hours before surgery, drinking tap water until 2 hours before surgery.

    Outcomes

    Primary Outcome Measures

    Mitotic Activity Index (MAI)
    Proliferation in invasive front in tumor

    Secondary Outcome Measures

    S-Insulin
    Secretion of insulin into serum; unit, mIE/L (milli international units pr liter)
    Well being after surgery
    Patient Reported Outcome Measures (Questionaire)
    High Resolution Magnetic Resonance Spectroscopy (HR-MRS) profiling of specific metabolites
    Metabolic profiling in the primary tumor and in the serum samples; measure content of lactate, glycine, choline, fatty acids and lipoproteins
    Relapse Free Survival
    Time from surgery to a relapse (Loco-regional, contralateral and systemic) is experienced
    Breast Cancer Specific Survival
    Time from surgery to dead of disease or all other causes of death.
    S-insulin c-peptide,
    Measure of total insulin secreted; unit, nM (nano molar)
    S-IGF1
    Measure of Insulin growth factor type 1; unit, nM (nano molar)
    S-IGFBP3
    Measure of Insulin growth factor binding protein 3; unit mg/L (milligram per liter)
    PR
    Expression of Progesteron Receptor in the primary tumor

    Full Information

    First Posted
    March 19, 2019
    Last Updated
    May 9, 2019
    Sponsor
    Helse Stavanger HF
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03886389
    Brief Title
    Breast Cancer Diet Intervention Study
    Acronym
    BCDIS
    Official Title
    The Effects of Insulin and Insulin-related Characteristics, and Short-Term Low-glycemic and High-glycemic Carbohydrate Intervention on Breast Cancer Biomarkers and Survival
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2019
    Overall Recruitment Status
    Completed
    Study Start Date
    June 12, 2009 (Actual)
    Primary Completion Date
    July 7, 2017 (Actual)
    Study Completion Date
    July 7, 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Helse Stavanger HF

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The investigators have already proven that Mitotic Activity Index (MAI)is the most robust measure of proliferation in breast cancer tissue. The purpose was to study whether 18 and 2-4 hours pre-operative per-oral carbohydrate loading (often given in gastrointestinal surgery i.e. enhanced recovery after surgery=ERAS) influences proliferation in the tumor, serum insulin characteristics, metabolic profile and survival.
    Detailed Description
    It has been postulated that a "Western-style" diet, rich in carbohydrates (especially high glycemic carbohydrates) may have an effect on the incidence of breast cancer, and perhaps also prognosis. This may be mediated through the insulin-related pathways in breast cells which may show insulin-dependent proliferation, which may alter outcome. Aims: To study: The inter-patient variation in insulin and insulin-related characteristics in the blood taken just before the operation from breast cancer patients, on a usual pre-operative fasting schedule; The influence of the variation in insulin and insulin-related characteristics on proliferation and other cell biological features in the breast cancers of these patients; Whether 4 and 18-hours pre-operative hyperglycaemic glucose loading (to reduce postoperative insulin resistance) influences proliferation (Mitotic Activity Index (MAI) and other cell biological features in breast cancer* The influence of the short-term effect of a pre-operative low-glycaemic carbohydrate isocaloric diet on proliferation and other cell biological features of the primary breast cancer cells (Low-glycemic isocaloric diet intervention study); Epidemiological risk factors: The correlation between epidemiological risk factors, insulin and insulin-related characteristics, proliferation, cell biological features and other biomarkers in breast cancer patients. Estrogen Receptor positive tumors will be analyses separately. Relapse free survival Breast Cancer Specific Survival. The Short-term effect of carbohydrates will be assessed in a randomized intervention study, where 30 patients receive oral carbohydrates 18 and 4 hours before surgery and 30 patients receive fasting procedure/water. Primary Outcome 1. Proliferation in the tumor as measured by MAI. Secondary Outcomes: Serum insulin characteristics (S-insulin, S- insulin c-peptide, S-IGF and S-IGFBP3) will be measured at various peri-surgical timepoints Changes in metabolic profile* in the tumor and in serum samples Patient Reported Outcome Measures (PROM) on well being Relapse free survival Breast Cancer Specific Survival Metabolic profile assessed by High Resolution Magnetic Resonance Spectroscopy (HR-MRS) in the tumor and in serum samples.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Early-stage Breast Cancer, Carbohydrate Engorgement, Proliferation, Insulin Resistance, Estrogen Receptor-positive Breast Cancer
    Keywords
    Breast Cancer, Estrogen receptor positive, Proliferation, Insulin resistance, PROMs, NMRI, RFS, BCSS

    7. Study Design

    Primary Purpose
    Basic Science
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Allocation: Randomized Intervention Model: Parallel Assignment Masking: None (Open Label) Primary Purpose: Treatment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    80 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Carbohydrate/intervention group
    Arm Type
    Experimental
    Arm Description
    Breast cancer patients receive 2 x preoperative carbohydrate loading [PreOP(TM)] before surgery; the 1st dose 18 hours before and 2nd dose 2-4 hours before surgery.
    Arm Title
    Control group
    Arm Type
    No Intervention
    Arm Description
    Breast cancer patients receive standard prep fasting procedure with nil food per os 8-10 hours before surgery, drinking tap water until 2 hours before surgery.
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    PreOP
    Intervention Description
    Mixture of Carbohydrates; standard amount designed for enhanced recovery after surgery (ERAS) i.e. preoperative carbohydrate loading before long standing surgery to enhance recovery.
    Primary Outcome Measure Information:
    Title
    Mitotic Activity Index (MAI)
    Description
    Proliferation in invasive front in tumor
    Time Frame
    Trough completion of surgery of all included patients, an average of 1,5 years
    Secondary Outcome Measure Information:
    Title
    S-Insulin
    Description
    Secretion of insulin into serum; unit, mIE/L (milli international units pr liter)
    Time Frame
    Analysed in serum samples at 5 time points; At inclusion (day 0), admission (day 10), preoperatively (day 11), postoperatively (day12) and at post operative visit (day 30)
    Title
    Well being after surgery
    Description
    Patient Reported Outcome Measures (Questionaire)
    Time Frame
    Day 1,2,3,4,5,6 and 7 after surgery
    Title
    High Resolution Magnetic Resonance Spectroscopy (HR-MRS) profiling of specific metabolites
    Description
    Metabolic profiling in the primary tumor and in the serum samples; measure content of lactate, glycine, choline, fatty acids and lipoproteins
    Time Frame
    Immediately after surgery: tumor is fresh frozen. High Resolution Magnetic Resonance Spectroscopy (HR-MRS) will be done in the fresh frozen tumor and deep frozen serum samples (=as for insulin characteristics)
    Title
    Relapse Free Survival
    Description
    Time from surgery to a relapse (Loco-regional, contralateral and systemic) is experienced
    Time Frame
    Until 8 years (97 months of follow up)
    Title
    Breast Cancer Specific Survival
    Description
    Time from surgery to dead of disease or all other causes of death.
    Time Frame
    8 years follow-up (97 months of follow up)
    Title
    S-insulin c-peptide,
    Description
    Measure of total insulin secreted; unit, nM (nano molar)
    Time Frame
    Analysed in serum samples at 5 time points; At inclusion (day 0), admission (day 10), preoperatively (day 11), postoperatively (day12) and at post operative visit (day 30)
    Title
    S-IGF1
    Description
    Measure of Insulin growth factor type 1; unit, nM (nano molar)
    Time Frame
    Analysed in serum samples at 5 time points; At inclusion (day 0), admission (day 10), preoperatively (day 11), postoperatively (day12) and at post operative visit (day 30)
    Title
    S-IGFBP3
    Description
    Measure of Insulin growth factor binding protein 3; unit mg/L (milligram per liter)
    Time Frame
    Analysed in serum samples at 5 time points; At inclusion (day 0), admission (day 10), preoperatively (day 11), postoperatively (day12) and at post operative visit (day 30)
    Title
    PR
    Description
    Expression of Progesteron Receptor in the primary tumor
    Time Frame
    Trough completion of surgery of all included patients, an average of 1,5 years

    10. Eligibility

    Sex
    Female
    Gender Based
    Yes
    Gender Eligibility Description
    Breast cancer is 100 x more frequent in women than in men.
    Minimum Age & Unit of Time
    25 Years
    Maximum Age & Unit of Time
    100 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: All consecutive operable patients in 2009-2010, with a clinical and/or radiologic and/or cytologic diagnosis of primary breast cancer, unless the exclusion criteria apply. Exclusion Criteria: Non-operable patients (i.e" patients with T3-4 (>5 cm) disease or distant metastases at the time of operation). All patients who refuse to participate. All patients with DCIS, micro-invasive cancer < 2mm diameter or tumors with histologic poor-quality material. Co-morbidity (Insulin dependent Diabetes Mellitus, Cushing syndrome, previous or concurrent cancers except CIN and non-melanomatous skin cancer. Mental inability to participate. Persons allergic to one of the compounds in any of the two diets.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Svein Skeie, PhD
    Organizational Affiliation
    Helse Stavanger HF; Stavanger University Hospital
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    IPD Sharing Plan Description
    All data will be available to all researches involved in the study included the statistician allocated to the study.
    Citations:
    PubMed Identifier
    16135467
    Citation
    Baak JP, van Diest PJ, Voorhorst FJ, van der Wall E, Beex LV, Vermorken JB, Janssen EA. Prospective multicenter validation of the independent prognostic value of the mitotic activity index in lymph node-negative breast cancer patients younger than 55 years. J Clin Oncol. 2005 Sep 1;23(25):5993-6001. doi: 10.1200/JCO.2005.05.511.
    Results Reference
    background
    PubMed Identifier
    18665447
    Citation
    Baak JP, Gudlaugsson E, Skaland I, Guo LH, Klos J, Lende TH, Soiland H, Janssen EA, Zur Hausen A. Proliferation is the strongest prognosticator in node-negative breast cancer: significance, error sources, alternatives and comparison with molecular prognostic markers. Breast Cancer Res Treat. 2009 May;115(2):241-54. doi: 10.1007/s10549-008-0126-y. Epub 2008 Jul 30.
    Results Reference
    background
    PubMed Identifier
    31801490
    Citation
    Lende TH, Austdal M, Bathen TF, Varhaugvik AE, Skaland I, Gudlaugsson E, Egeland NG, Lunde S, Akslen LA, Jonsdottir K, Janssen EAM, Soiland H, Baak JPA. Metabolic consequences of perioperative oral carbohydrates in breast cancer patients - an explorative study. BMC Cancer. 2019 Dec 4;19(1):1183. doi: 10.1186/s12885-019-6393-7.
    Results Reference
    derived
    PubMed Identifier
    31703648
    Citation
    Lende TH, Austdal M, Varhaugvik AE, Skaland I, Gudlaugsson E, Kvaloy JT, Akslen LA, Soiland H, Janssen EAM, Baak JPA. Influence of pre-operative oral carbohydrate loading vs. standard fasting on tumor proliferation and clinical outcome in breast cancer patients horizontal line a randomized trial. BMC Cancer. 2019 Nov 8;19(1):1076. doi: 10.1186/s12885-019-6275-z.
    Results Reference
    derived

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