A Window of Opportunity Study of Methionine Deprivation in Triple Negative Breast Cancer

Status: Terminated
Location: See location...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Given preliminary data demonstrating that methionine deprivation enhances cell surface expression of TRAIL receptor-2, the objective of this clinical trial is to confirm that methionine restriction enhances its expression in triple negative breast cancer and to establish the feasibility and acceptability of this dietary intervention in humans. This study will also examine the effect of methionine restriction on cancer stem cells and metabolic health.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Participants must have histologically confirmed operable triple negative breast cancer

‣ ER (estrogen receptors) and PR (progesterone receptors) expression must be \< 2%

⁃ HER2 must negative as shown be either 0 or 1+ by immunohistochemistry (if 2+, in situ hybridization method used to define HER2) OR by a HER2: 17 centromere signal of \<2.0 using a standard in situ hybridization method.

• No prior therapy for current breast cancer

• Operable breast cancer. Participants who are planned to undergo neo-adjuvant chemotherapy are eligible as long as they consent to an additional breast biopsy following the dietary intervention immediately prior to starting chemotherapy

• ECOG (Eastern Cooperative Oncology Group) performance status ≤1

• Ability to understand and the willingness to sign a written informed consent document

• Serum creatinine \<ULN (upper limit of normal)

• Non-pregnant. Women of childbearing potential must have a negative pregnancy test to participate in this study

• Women of childbearing potential must agree to use effective contraceptives (as discussed with their physician) while participating in this study

Locations
United States
Wisconsin
University of Wisconsin Carbone Cancer Center
Madison
Time Frame
Start Date: 2017-08-10
Completion Date: 2019-06-21
Participants
Target number of participants: 6
Treatments
Experimental: Hominex-2
Participants will receive an individualized dietary prescription that incorporates a methionine-free amino acid-modified medical food (Hominex-2, Abbott Nutrition) supplemented with low-methionine foods. Hominex-2 contains a mixture of L-amino acids but lacks methionine.~Participants will be asked to have an optional non-contrast MRI to assess body composition prior to and at completion of the methionine-restricted (MR) diet. Not completing a scheduled MRI is not considered a protocol deviation.~Participants will be followed for 30 days after surgery or biopsy date. Subjects removed from study for unacceptable adverse events (AEs) will be followed until resolution or stabilization of the AE.
Sponsors
Leads: University of Wisconsin, Madison
Collaborators: Avon Foundation

This content was sourced from clinicaltrials.gov

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