Keto-Brain:Investigating the Use of Ketogenic Diets in Brain Metastases
Primary Purpose
Brain Metastases, Adult
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Laboratory Biomarker Analysis
Neurocognitive Assessment
Questionnaire Administration
Fitbit
Dietary Intervention
Sponsored by
About this trial
This is an interventional supportive care trial for Brain Metastases, Adult
Eligibility Criteria
Inclusion Criteria:
- Measurable brain lesions noted on baseline MRI imaging
- Graded Prognostic Assessment > 1.5
- Body mass index (BMI) ≥18 kg/m2
- Eastern Cooperative Oncology Group (ECOG) Performance status of 0-1 (0=participant has either normal activity, 1= participant has some symptoms but is nearly full ambulatory)
- Able and willing to follow prescribed diet intervention
- Scheduled to receive SRS
Exclusion Criteria:• Undergoing whole brain radiation therapy
- BMI <18 kg/m2
- Pregnant or nursing women
- Not willing to be randomized into either of the dietary interventions
- Unable to provide Informed Consent
- No previous diagnosis of small cell lung carcinoma
- No previous or suspected leptomeningeal disease
- Type 1 diabetes or insulin-dependent Type II diabetes
- Abnormal renal function (GFR < 55 mL/min, creatinine >2.0, urinary albumin >1 g/day) Not MRI eligible
Sites / Locations
- Ohio State University Comprehensive Cancer CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Standard of Care
Standard of Care + Ketogenic Diet
Arm Description
Patients receive standard of care therapy with SRS and AICR Diet education.
(standard of care, ketogenic diet) Patients receive standard of care with SRS. Patients undergo a controlled feeding period ketogenic diet comprising of meals for the first week and then transition into a free living with guided support type of intervention.
Outcomes
Primary Outcome Measures
Feasibility of maintaining a ketogenic versus AICR diet in patients with brain metastasis selected for radiosurgery
Summaries from questionnaires will be plotted over time to assess adherence and compliance to the ketogenic diet.
Feasibility of maintaining a ketogenic diet in patients with brain metastasis selected for radiosurgery
Summaries from ketone logs will be plotted over time to assess adherence and compliance to the ketogenic diet.
Metabolic outcomes of a ketogenic versus AICR diet in patients with brain metastasis selected for radiosurgery
Summaries from blood markers will be plotted over time to assess adherence and compliance to the ketogenic diet.
Number of Participants with partial-or-complete response according to RECIST v1.1
use a Chi-squared test for the association between treatment group and partial-or-complete response according to RECIST v1.1
Secondary Outcome Measures
Preliminary effects of the ketogenic versus AICR diet on Neurocognitive Function Scores in BM individuals undergoing radiation therapy
same linear mixed effects model as for the primary objective, but with the following quality-of-life endpoints as outcomes
Preliminary effects of the ketogenic versus AICR diet on PROMIS Cognitive Function Short Form 8a Scores in BM individuals undergoing radiation therapy
same linear mixed effects model as for the primary objective, but with the following quality-of-life endpoints as outcomes
Preliminary effects of the ketogenic versus AICR diet on Heart Hope Scale in BM individuals undergoing radiation therapy to asses quality of life
same linear mixed effects model as for the primary objective, but with the following quality-of-life endpoints as outcomes
Full Information
NCT ID
NCT05428852
First Posted
June 14, 2022
Last Updated
February 3, 2023
Sponsor
Ohio State University Comprehensive Cancer Center
1. Study Identification
Unique Protocol Identification Number
NCT05428852
Brief Title
Keto-Brain:Investigating the Use of Ketogenic Diets in Brain Metastases
Official Title
Keto-Brain: Investigating the Use of Ketogenic Diets in Brain Metastases
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 26, 2022 (Actual)
Primary Completion Date
July 2024 (Anticipated)
Study Completion Date
July 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ohio State University Comprehensive Cancer Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This pilot study will be a single center, randomized controlled study of 24 participants with diagnosed BM (various primary disease sites) comparing the effect of a ketogenic (n=12) and AICR (n=12) diet. Potential participants will be identified via medical record reviews and chart reviews. Eligibility of patients will be assessed via medical record review. Randomization will be balanced by blocks of random sizes but no stratification due to the small sample size. Both groups will undergo a 16-week diet intervention where research dietitians will provide educations, recipes and grocery lists on the participants assigned diet. Each group will receive 4-7 days worth of food prior to testing days to both aid in transitioning to each dietary arm and to ensure that the metabolic needs for each arm are met. In an effort to maintain a patient centric focus and monitor changes in quality of life (QOL) all patients will complete psychosocial and behavioral inventories. These inventories aim to capture a holistic view on the proposed nutritional intervention during treatment. Primary outcomes will be determined at baseline, 8 weeks, and 16 weeks while patient-centric outcomes will be assessed every four weeks. Participants will have counseling by the attending physician for additional applicable medications for any treatment related side effects or toxicities. The intervention groups will undergo their randomized dietary regimen for 16 weeks.
Detailed Description
Neurological tissues are among the most common (>10% of cancer patients) and debilitating sites for metastatic disease to develop. The brain is a 'sanctuary site' for many cancer cells and remains a challenging site to treat. Surgery and radiation therapies are the most common treatments. The investigators hypothesize that the metabolic adaptations associated with a well-formulated ketogenic diet that induces nutritional ketosis will significantly improve the response to surgery and radiation in patients with brain metastases. To date, numerous preclinical studies have demonstrated the ability of nutritional ketosis and caloric restriction to augment the therapeutic efficacy of radiotherapy. Use of a ketogenic diet is known to decrease the protein expression of HIF-1 and VEGFR2, and may increase radio sensitivity by normalizing tumor vasculature and increasing facilitated oxygen delivery to tumor cells. Several additional proposed mechanisms exist for enhancing radiosensitivity of the malignancy including: HDAC dependent mechanisms, ATP deprivation, mitochondrial ROS production and downregulation of IGF-1 receptor. Short-term fasting, a way to increase ketones acutely, has been demonstrated to speed up mitotic rates and thus facilitate a DNA damage sensitization. Lastly, a recent study showed that glucose restriction lowered Ki-67 expression, clonogenic frequency and rate of proliferation in gliomaspheres in vitro.
The investigating team team has an established expertise in conducting ketogenic diet interventions. Many individuals have adopted a low-carbohydrate diet for health reasons, yet there is scarce professional support available to provide guidance and support, especially for ketogenic diets. The investigators have scientific expertise and practical knowledge of both ketogenic and current standard of care cancer diets combined with a passion to empower people with the tools to implement these eating approaches into the participant's lifestyle. This project is highly patient-centered. The investigators will support patients who are randomized into either one of the intervention groups and provide them with a personalized eating plan designed to have maximal therapeutic impact and positively impact their lives. To that end, this project is unique in that it is highly patient-centered while also designed to have a substantial scientific and practical impact on medical management of brain metastasis treatments.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Metastases, Adult
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
24 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Standard of Care
Arm Type
Active Comparator
Arm Description
Patients receive standard of care therapy with SRS and AICR Diet education.
Arm Title
Standard of Care + Ketogenic Diet
Arm Type
Experimental
Arm Description
(standard of care, ketogenic diet) Patients receive standard of care with SRS. Patients undergo a controlled feeding period ketogenic diet comprising of meals for the first week and then transition into a free living with guided support type of intervention.
Intervention Type
Other
Intervention Name(s)
Laboratory Biomarker Analysis
Intervention Description
Correlative Studies
Intervention Type
Other
Intervention Name(s)
Neurocognitive Assessment
Intervention Description
NRG-CC
Intervention Type
Other
Intervention Name(s)
Questionnaire Administration
Intervention Description
Ancillary studies
Intervention Type
Device
Intervention Name(s)
Fitbit
Intervention Description
Fitbit Activity Tracking
Intervention Type
Dietary Supplement
Intervention Name(s)
Dietary Intervention
Intervention Description
Undergo ketogenic diet
Primary Outcome Measure Information:
Title
Feasibility of maintaining a ketogenic versus AICR diet in patients with brain metastasis selected for radiosurgery
Description
Summaries from questionnaires will be plotted over time to assess adherence and compliance to the ketogenic diet.
Time Frame
Up to 16 weeks
Title
Feasibility of maintaining a ketogenic diet in patients with brain metastasis selected for radiosurgery
Description
Summaries from ketone logs will be plotted over time to assess adherence and compliance to the ketogenic diet.
Time Frame
Up to 16 weeks
Title
Metabolic outcomes of a ketogenic versus AICR diet in patients with brain metastasis selected for radiosurgery
Description
Summaries from blood markers will be plotted over time to assess adherence and compliance to the ketogenic diet.
Time Frame
Up to 16 weeks
Title
Number of Participants with partial-or-complete response according to RECIST v1.1
Description
use a Chi-squared test for the association between treatment group and partial-or-complete response according to RECIST v1.1
Time Frame
Baseline up to 16 weeks
Secondary Outcome Measure Information:
Title
Preliminary effects of the ketogenic versus AICR diet on Neurocognitive Function Scores in BM individuals undergoing radiation therapy
Description
same linear mixed effects model as for the primary objective, but with the following quality-of-life endpoints as outcomes
Time Frame
Baseline up to 16 weeks
Title
Preliminary effects of the ketogenic versus AICR diet on PROMIS Cognitive Function Short Form 8a Scores in BM individuals undergoing radiation therapy
Description
same linear mixed effects model as for the primary objective, but with the following quality-of-life endpoints as outcomes
Time Frame
Baseline up to 16 weeks
Title
Preliminary effects of the ketogenic versus AICR diet on Heart Hope Scale in BM individuals undergoing radiation therapy to asses quality of life
Description
same linear mixed effects model as for the primary objective, but with the following quality-of-life endpoints as outcomes
Time Frame
Baseline up to 16 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Measurable brain lesions noted on baseline MRI imaging
Graded Prognostic Assessment > 1.5
Body mass index (BMI) ≥18 kg/m2
Eastern Cooperative Oncology Group (ECOG) Performance status of 0-1 (0=participant has either normal activity, 1= participant has some symptoms but is nearly full ambulatory)
Able and willing to follow prescribed diet intervention
Scheduled to receive SRS
Exclusion Criteria:• Undergoing whole brain radiation therapy
BMI <18 kg/m2
Pregnant or nursing women
Not willing to be randomized into either of the dietary interventions
Unable to provide Informed Consent
No previous diagnosis of small cell lung carcinoma
No previous or suspected leptomeningeal disease
Type 1 diabetes or insulin-dependent Type II diabetes
Abnormal renal function (GFR < 55 mL/min, creatinine >2.0, urinary albumin >1 g/day) Not MRI eligible
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
The Ohio State University Comprehensive Cancer Center
Phone
800-293-5066
Email
OSUCCCClinicaltrials@osumc.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Madison Kackley, PhD
Phone
6142479650
Email
kackley.19@osu.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeff Volek, PhD
Organizational Affiliation
Ohio State University Comprehensive Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ohio State University Comprehensive Cancer Center
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jeff Volek, PhD
Phone
614-688-1701
Email
volek.1@osu.edu
First Name & Middle Initial & Last Name & Degree
Madison Kackley, PhD
Phone
614-247-9650
Email
kackley.19@osu.edu
12. IPD Sharing Statement
Links:
URL
http://cancer.osu.edu
Description
The Jamesline
Learn more about this trial
Keto-Brain:Investigating the Use of Ketogenic Diets in Brain Metastases
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