The KetoGlioma (Ketogenic Glioma) Study
Primary Purpose
Glioma
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Supplemental High Fat Low Carbohydrate (sHFLC) + KetoPhyt
Sponsored by
About this trial
This is an interventional other trial for Glioma focused on measuring Glioma, KetoPhyt, High-grade gliomas
Eligibility Criteria
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
Sites / Locations
- Tufts Medical CenterRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Supplemental High Fat Low Carbohydrate (sHFLC) + KetoPhyt
Arm Description
Subjects will adhere to the sHFLC + KetoPhyt diet for six 4-week cycles.
Outcomes
Primary Outcome Measures
Number of participants not able to adhere the sHFLC + KetoPhyt Diet
Patients' ability to adhere to the sHFLC + KetoPhyt Diet as defined by the presence of the following:
>75% compliance with taking supplement 2x/day throughout the study period
>75% of days with carbohydrate intake <33%
Secondary Outcome Measures
Change from baseline between the patient's glucose and ketone levels at 24 weeks as assessed by the Glucose/Ketone Index (GKI)
Blood glucose and ketone levels measured at the same time once per day from baseline to 24 weeks via a glucose/ketone monitor and test strips. The Glucose/Ketone Index will be used to monitor patient's glucose and ketone levels.
Change from baseline in pro-inflammatory markers and exosome biomarkers at 24 weeks
Comparison of the numbers of EGFrVIII+ exosomes and exosomal microRNAs in each participant's blood measured at baseline (Cycle 1 Day 1) and 24 weeks (Cycle 6).
Change from baseline between the patient's gut microbiome at 24 weeks as assessed by 16s ribosomal sequences.
DNA purified from stool samples (16s ribosomal sequences) will be compared at baseline and 24 weeks.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05373381
Brief Title
The KetoGlioma (Ketogenic Glioma) Study
Official Title
A Modified Ketogenic, Anti-Inflammatory Diet for Patients With High-Grade Gliomas
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 18, 2022 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 30, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tufts Medical Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
Detailed 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glioma
Keywords
Glioma, KetoPhyt, High-grade gliomas
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Supplemental High Fat Low Carbohydrate (sHFLC) + KetoPhyt
Arm Type
Experimental
Arm Description
Subjects will adhere to the sHFLC + KetoPhyt diet for six 4-week cycles.
Intervention Type
Dietary Supplement
Intervention Name(s)
Supplemental High Fat Low Carbohydrate (sHFLC) + KetoPhyt
Intervention Description
Following a screening period, subjects will adhere to the sHFLC + KetoPhyt diet for six 4-week cycles. Patients will receive dietary advice from a Registered Dietitian (RD) to allow for the design of personalized meal plans maintaining carbohydrates up to 33% of total caloric intake, and be asked to maintain a daily dietary log. To assist patients in understanding, monitoring and controlling their dietary choices to maintain a low carbohydrate diet, they will be trained and receive assistance on the use of an online tool for tracking nutrition [Healthtrac].
Primary Outcome Measure Information:
Title
Number of participants not able to adhere the sHFLC + KetoPhyt Diet
Description
Patients' ability to adhere to the sHFLC + KetoPhyt Diet as defined by the presence of the following:
>75% compliance with taking supplement 2x/day throughout the study period
>75% of days with carbohydrate intake <33%
Time Frame
From Cycle 1 Day 1 to end of Cycle 6 (Each cycle is 28 days)
Secondary Outcome Measure Information:
Title
Change from baseline between the patient's glucose and ketone levels at 24 weeks as assessed by the Glucose/Ketone Index (GKI)
Description
Blood glucose and ketone levels measured at the same time once per day from baseline to 24 weeks via a glucose/ketone monitor and test strips. The Glucose/Ketone Index will be used to monitor patient's glucose and ketone levels.
Time Frame
Measured daily from Cycle 1 Day 1 to end of Cycle 6 (Each cycle is 28 days)
Title
Change from baseline in pro-inflammatory markers and exosome biomarkers at 24 weeks
Description
Comparison of the numbers of EGFrVIII+ exosomes and exosomal microRNAs in each participant's blood measured at baseline (Cycle 1 Day 1) and 24 weeks (Cycle 6).
Time Frame
At Cycle 1 Day 1 and at Cycle 6 Day 1 (Each cycle is 28 days)
Title
Change from baseline between the patient's gut microbiome at 24 weeks as assessed by 16s ribosomal sequences.
Description
DNA purified from stool samples (16s ribosomal sequences) will be compared at baseline and 24 weeks.
Time Frame
Measured daily from Cycle 1 Day 1 to end of Cycle 6 (Each cycle is 28 days)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Latoya Lashley, MPH
Phone
617-636-3264
Email
ncccr@tuftsmedicalcenter.org
Facility Information:
Facility Name
Tufts Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02111
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Latoya Lashley, MPH
Phone
617-636-3264
Email
ncccr@tuftsmedicalcenter.org
First Name & Middle Initial & Last Name & Degree
Suriya Jeyapalan, MD
12. IPD Sharing Statement
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The KetoGlioma (Ketogenic Glioma) Study
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