Skip to main content
OpenTrials
Completed

NCT Number: NCT03045289

A Whole-food, Plant-Based Nutrition Intervention in Women With Metastatic Breast Cancer

This research will examine the feasibility of conducting a strict whole-food, plant-based dietary intervention in women with stable metastatic breast cancer currently undergoing conventional treatments. In addition, this research will provide preliminary data on dietary intakes and the effect of plant-based nutrition on numerous outcomes reflecting cancer prognosis and overall health using advanced imaging, various blood biomarkers linked to cancer progression, and numerous symptom questionnaires.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University of Rochester

Rochester, New York, 14642, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women with a confirmed diagnosis of metastatic breast cancer with a stable treatment regimen, demonstrated by no changes in primary cancer therapy 6 weeks prior to consent and no anticipated changes in primary cancer therapy in the 4 weeks following consent.
  • Systemic therapy may consist of any conventional treatment including anti-hormonal, cytotoxic, targeted monoclonal antibody or small molecule kinase inhibitors or any combination of the above. Women who have previously declined conventional cancer therapy are also eligible provided they meet all other eligibility criteria.
  • Expected to survive for at least 6 months.
  • Eligibility classification for enrollment into the study - T: any; N: any; M:1.
  • Any ER/PR/HER2 status is eligible.
  • Age > 18 years.
  • Must be willing to adopt a strict, whole-foods, plant-based diet.
  • Participant must be willing and able to comply with the protocol for the duration of the study including scheduled testing and weekly office visits.
  • Able to speak and read English fluently.

Exclusion criteria

  • Inability to tolerate a normal diet.
  • Current use of insulin or sulfonylureas.
  • Active malabsorption syndrome at time of consent (ie. Crohn's disease, major bowel resection leading to permanent malabsorption).
  • Current eating disorder.
  • Uncontrolled diarrhea.
  • Plant-based food allergies or intolerances.
  • Recent consumption (in the past 6 months) of a vegan diet.
  • GFR < 30 on 2 or more lab tests in the past 90 days.
  • Serum potassium > 5.3 on 2 or more lab tests in the past 90 days.
  • Major surgery within 2 months of starting study program.
  • Psychiatric disorder that prohibits giving informed consent.
  • Current smoking.
  • Current high risk alcohol use (> 7 drinks per week).
  • Current illicit substance use.
  • Current warfarin use.

Treatment and study plan

Plant-based diet

Behavioral

Women will be provided with 3 meals daily, delivered to their home, for 8 weeks, along with a multivitamin, and will attend weekly office visits.

Primary outcomes

  1. Recruitment

    Time frame: 1 year

    Percentage of women who are randomized in the study out of the all women approached.

  2. Retention

    Time frame: 8 weeks

    Percentage of women who start the intervention who go on to complete 8-week testing

  3. Compliance

    Time frame: 8 weeks

    The percentage of daily calorie intake from "on-plan" food will be calculated for each participant.

Secondary outcomes

  1. FACT-B

    Time frame: 8 weeks

  2. EORTC QLQ-C30

    Time frame: 8 weeks

  3. FACT-COG

    Time frame: 8 weeks

  4. Brief Fatigue Inventory (BFI)

    Time frame: 8 weeks

  5. Symptom Inventory

    Time frame: 8 weeks

  6. Serum breast cancer biomarkers

    Time frame: 8 weeks

    CA 15-3, CEA, CA 27.29

  7. Tumor Metabolic Activity as assessed by Positron Emission Tomography/ Computer Tomography (PET/CT)

    Time frame: 8 weeks

  8. Changes in nutrient intakes based on 3 day food diaries

    Time frame: 8 weeks

    Assess baseline diet compared to intervention diet

  9. Weight

    Time frame: 8 weeks

  10. Blood Pressure

    Time frame: 8 weeks

  11. Inflammatory Markers

    Time frame: 8 weeks

    CBC, CRP

  12. Hormonal Levels

    Time frame: 8 weeks

    Estradiol, testosterone, SHBG, DHEAS, Insulin, IGF-1, IGFBP-3

  13. Metabolic Markers

    Time frame: 8 weeks

    Lipids, CMP

  14. Tumor Metabolic Activity

    Time frame: 8 weeks

    PET/CT scan SUV Uptake

  15. Circulating Tumor Cells

    Time frame: 8 weeks

  16. cell-free DNA

    Time frame: 8 weeks

Sponsors and collaborators

Lead sponsor

University of Rochester

Other

Collaborators

  • Johns Hopkins University

Registry information

Official study title

Whole-Food, Plant-Based Nutrition Among Women With Metastatic Breast Cancer: A Pilot Study of Recruitment, Retention, and Preliminary Changes in Biomarkers and Symptoms.

Important dates

Study start
2018
Primary completion
2022
Study completion
2022
First posted
Feb 7, 2017
Registry last updated
Jul 13, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.