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The KetoGlioma (Ketogenic Glioma) Study

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Tufts University

Status

Withdrawn

Conditions

Glioma

Treatments

Dietary Supplement: Supplemental High Fat Low Carbohydrate (sHFLC) + KetoPhyt

Study type

Interventional

Funder types

Other

Identifiers

NCT05373381
KetoGlioma
STUDY00001948 (Other Identifier)

Details and patient eligibility

About

This research is being conducted to see if patients diagnosed with high grade gliomas can adhere to the supplemented High-Fat Low-Carbohydrate (sHFLC) + KetoPhyt diet, and to see how this diet might affect cancer cells in the bloodstream. This diet is experimental and is not routinely prescribed for patients with high-grade gliomas. The results of this study may be used to support larger studies investigating possible anti-tumor affects of the sHFLC + KetoPhyt diet.

Full description

This study is designed to analyze the feasibility of using the sHFLC + KetoPhyt as an anti-cancer agent against glioblastoma multiforme (GBM). While the classic ketogenic diet typically uses a 4:1 ratio of fat to proteins/carbohydrates, the sHFLC + KetoPhyt diet has a maximum 2:1 ratio. This allows increased flexibility in the diet and improved nutritional sufficiency. Preclinical and controlled patient data supports that the sHFLC + KetoPhyt diet is able to decrease blood glucose levels while increasing circulating ketones, two key effects of the ketogenic diet. As caloric restriction is not used in this approach, the investigators hypothesize that patients will be able to have an increased dietary compliance compared to those patients on the very restrictive ketogenic diet, but still achieve a ketotic state.

There is general consensus in the field that the use of the phyto anti-inflammatory diet and exogenous ketone supplementation can all lead to ketosis in a matter of days, and not become what is referred to as ketone adaptative for many weeks to months. Ketosis, with blood levels of the ketone body beta-hydroxy- butarate >0.5 mM, undergoes an adaptive process where different tissues at different times alter the biochemistry of their cellular fuel sources following the switching from a glucose- to fat- and lipid-metabolism. This affects the ability to precisely measure different states of ketosis in the study population over time as the adaptive processes are temporally unique, however previous studies have described the "...adaptation periods necessary... for particular tissue ketone oxidation following sustained nutritional ketosis..." , and these investigators even related this to inflammation-associated cytokine expressions as the investigators propose to measure in this study.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with high-grade gliomas (World Health Organization [WHO] Grade III/IV) with newly diagnosed or recurrent disease

  • Ability to understand and willingness to sign an informed consent form prior to any study procedures

  • For patients treated with external beam radiation (XRT), interstitial brachytherapy or radiosurgery, an interval of > 4 weeks must have elapsed from completion of XRT to pre-registration.

  • Eastern Cooperative Oncology Group (ECOG) Performance Status ≤ 2

  • Recovered to Common Terminology Criteria for Adverse Events (CTCAE) grade 1 or less toxicity from other agents with exception of alopecia.

  • Steroid dosing stable for at least 7 days

  • Adequate organ function as defined by the following laboratory values:

    • Absolute neutrophil count (ANC) ≥ 1500/mm3
    • Platelet Count ≥ 100,000/mm3
    • Creatinine ≤ 1.5 mg/dl x upper limit of normal (ULN)
    • Creatinine Clearance ≥ 45 mL/min
    • Total Bilirubin ≤ 1.5 x ULN (except in cases of Gilbert's disease)
    • AST (aspartate aminotransferase)/ ALT (alanine transaminase) ≤ 2.5 x ULN

Exclusion criteria

  • Concurrent investigational agents or other glioma-directed therapy (chemotherapy, radiation) while on study.
  • Pregnant or breastfeeding

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 1 patient group

Supplemental High Fat Low Carbohydrate (sHFLC) + KetoPhyt
Experimental group
Description:
Subjects will adhere to the sHFLC + KetoPhyt diet for six 4-week cycles.
Treatment:
Dietary Supplement: Supplemental High Fat Low Carbohydrate (sHFLC) + KetoPhyt

Trial contacts and locations

1

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Central trial contact

Latoya Lashley, MPH

Data sourced from clinicaltrials.gov

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