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A Pilot and Feasibility Neoadjuvant Study of a 2-Week Ketogenic Diet in Combination With Letrozole to Modulate PI3K Signaling in ER+ Breast Cancer
This is a neoadjuvant study to determine the feasibility and tolerability of 2 weeks of a very low carbohydrate ketogenic diet in combination with letrozole for patients with early stage operable ER+disease.
Primary Objective: • To evaluate the feasibility and tolerability of a 2 week ketogenic diet in combination with endocrine therapy prior to surgery for early stage ER+ breast cancer. Secondary Objectives * To determine whether endocrine therapy in combination with a dietary intervention to reduce insulin pathway signaling results in enhanced inhibition of cancer cell proliferation (measured byKi67) * To determine the effectiveness of 2 weeks of a ketogenic diet to reduce measures of insulin/PI3Kpathway activation in breast tumors * To measure changes in weight and body composition after 2 weeks of a ketogenic diet * To measure changes in insulin resistance after 2 weeks of a ketogenic diet * To measure the effectiveness of a ketogenic diet in combination with endocrine therapy to induce and maintain a ketogenic state. Outline: Participants will have baseline metabolic parameters measured and will begin a 2-week diet consisting of meal replacement shakes to induce a ketogenic state. Patients will also receive letrozole 2.5 mg daily. At the end of 2 weeks, metabolic parameters will again be measured and patients will proceed with surgical treatment of their breast cancer. A tumor biopsy from the surgical specimen will be obtained to measure cell proliferation compared with the pre-treatment diagnostic biopsy.
Age
18 - No limit years
Sex
FEMALE
Healthy Volunteers
No
Vanderbilt-Ingram Cancer Center
Nashville, Tennessee, United States
Start Date
July 8, 2019
Primary Completion Date
March 7, 2024
Completion Date
July 14, 2024
Last Updated
October 15, 2024
31
ACTUAL participants
2-Week Ketogenic Diet
DIETARY_SUPPLEMENT
Letrozole
DRUG
Lead Sponsor
Vanderbilt-Ingram Cancer Center
NCT03719495
NCT02235051
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