Ketogenic Diets as an Adjuvant Therapy in Glioblastoma (KEATING)
Primary Purpose
Glioblastoma, Glioblastoma Multiforme, Glioblastoma, Adult
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
MKD
MCT
Sponsored by
About this trial
This is an interventional treatment trial for Glioblastoma focused on measuring ketogenic
Eligibility Criteria
Inclusion Criteria:
- Age ≥16 years
- Patient at The Walton Centre NHS Foundation Trust
- Performance status ≤2
- Confirmed histological diagnosis of glioblastoma
- Undergone surgical resection or biopsy and will go onto receive/ is receiving/ has received oncological treatments
Exclusion Criteria:
- Having prior use of KD
- Kidney dysfunction
- Liver dysfunction
- Gall bladder dysfunction
- Metabolic disorder
- Eating disorder
- Diabetes (requiring medication)
- Body mass index ≤ 18.5kg/m2
- Weight loss medications
- Currently pregnant or breast feeding
- Performance status ≥3
Sites / Locations
- Univeristy of Liverpool/ The Walton Centre NHS Foundation Trust
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Modified ketogenic diet (MKD)
Medium chain triglyceride (MCT) diet
Arm Description
MKD: 80% fat and 5% carbohydrate (% of total energy requirements per day).
MCT: 75% fat (30% of which is medium chain fatty acids taken as a supplement) and 5% carbohydrate (% of total energy requirements per day).
Outcomes
Primary Outcome Measures
To assess retention and drop out rates
Number of patients who start randomized treatment as a proportion of the number randomized ;
To assess retention and drop out rates
The number of patients who complete 12 weeks as a proportion of the number randomized
To assess retention and drop out rates
Description of barriers and facilitators to data collection and participant retention
To assess retention and drop out rates
The time to dietary discontinuation
Secondary Outcome Measures
Estimation of recruitment rates
Actual recruitment compared to proposed recruitment
Enrollment of patients
Number of patients initiated on diet prior to starting oncological treatments.
Enrollment of patients
Number of patients initiated on diet during oncological treatments.
Enrollment of patients
Number of patients initiated on diet post oncological treatments.
Long term retention
Time to dietary discontinuation after week 12
Dietary adjustments required to achieve ketosis
Number of dietary adjustments to macronutrient composition of MCT and MKD diets required to achieve ketosis.
Self reported dietary compliance
Self reported by compliance rate
Calculated dietary compliance
Analysed by comparing macronutrient content assessed via 3 day food diaries to advised macronutrient content.
MCT compliance
Dose of MCT taken compared to dose advised.
Ketosis levels
Self reported urinary ketone levels twice daily for first 6 weeks then once per week thereafter and blood ketone and glucose levels weekly.
Dietetic time required for interventions
Dietetic time spent on clinical and non clinical activities relating to the trial.
Protocol refinements required
Number of deviations from the protocol including reasons for deviations.
Sample size estimates for future trials
Number of participants required for future phase III clinical trials
Quality of life
Change in quality of life assessed through EORTC QLQ C30 and BN 20 questionnaires
Food acceptability
Change in food acceptability assessed through food acceptability questionnaire
Gastrointestinal side effects
Number of reported gastrointestinal side effects assessed through EORTC QLQ C30 questionnaire and Common Terminology Criteria for Adverse Events.
Changes to biochemical markers
Changes to biochemical markers (renal, bone, LFT, lipid profiles) during the duration of the diet.
Anthropometric changes
Changes to anthropometry (weight, body mass index, fat mass, muscle circumference, hand grip strength) during the duration of the diet.
Completeness of data
Number of complete data sets for all trial outcomes
Full Information
NCT ID
NCT03075514
First Posted
February 28, 2017
Last Updated
April 2, 2019
Sponsor
University of Liverpool
Collaborators
Walton Centre NHS Foundation Trust, Vitaflo International, Ltd
1. Study Identification
Unique Protocol Identification Number
NCT03075514
Brief Title
Ketogenic Diets as an Adjuvant Therapy in Glioblastoma
Acronym
KEATING
Official Title
Ketogenic Diets as an Adjuvant Therapy in Glioblastoma: A Randomised Pilot Trial
Study Type
Interventional
2. Study Status
Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
April 1, 2017 (Actual)
Primary Completion Date
March 5, 2019 (Actual)
Study Completion Date
March 5, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Liverpool
Collaborators
Walton Centre NHS Foundation Trust, Vitaflo International, Ltd
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
Glioblastoma (GB) is the commonest form of brain cancer in adults. Despite current treatment options including surgery, radiotherapy and chemotherapy, overall survival is poor. Therefore, other treatment options are being explored and there is increasing interest in the possibility of using the ketogenic diet (KD), alongside current treatment options.
The KD is a high fat, low carbohydrate diet. This encourages the body to use fat (broken down to ketones) as its primary energy source, instead of carbohydrate (broken down to glucose, a type of sugar). KDs have been considered for use in patients with GB as this type of cancer is thought to use glucose as its main energy supply, which is of short supply in this diet. Animal studies have shown KDs may make GB more responsive to radiotherapy and chemotherapy and could improve survival by slowing the cancer's growth. However, clinical studies are needed in humans to assess any possible benefits.
This trial will see patients randomly assigned to one of two types of KDs; the modified ketogenic diet (MKD) and the medium chain triglyceride ketogenic diet (MCT). Both diets follow the same high fat, low carbohydrate principles, with the MCT diet requiring the patient to take some of the fat as a supplement drink instead of as food. Patients will follow the diet for 12 weeks initially. The trial will look to enroll newly diagnosed GB patients, from The Walton Centre NHS Foundation Trust over a 12 month period.
The aim of the trial is to investigate protocol feasibility and patient impact by comparing two KDs in an NHS setting, with a view to informing future phase III clinical trials.
Detailed Description
A prospective, non-blinded, randomized, pilot study will be undertaken in patients with glioblastoma (GB). Patients will be randomized to the modified ketogenic diet (MKD) or the medium chain triglyceride ketogenic diet (MCT) for a 12 week period (primary completion). If patients wish to remain on diet, they will be offered dietetic support for a total of 12 months (secondary completion).
The trial will be open to all Walton Centre Foundation Trust patients with a newly diagnosed GB, who have undergone surgical resection or biopsy within the last four months and who are going on to receive/ are currently receiving/ have completed oncological treatments (radiotherapy or chemotherapy or chemoradiotherapy). Patients will be referred via neuro-oncology multi-disciplinary meetings and neurosurgical clinics, post histology. The diet will be offered alongside standard care, commencing within four months of surgery.
Both diets are high in fat and low in carbohydrate, but contain different types and amounts of fats. The MKD is 80% fat (predominately long chain fatty acids) and 5% carbohydrate, whilst the MCT diet is 75% fat (30% of which is medium chain fatty acids) and 10% carbohydrate.
A permuted block randomization method will be adopted, using 'sealedenvelope' randomization system. This will be set up and administered by the statistician, who is not involved with the recruiting of patients.
Patients will receive regular input from the trial dietitian. This includes clinical consultations at baseline, dietary initiation, week 6, week 12 and every 3 months thereafter and telephone consultations at weeks 1, 3 and 9. Patients will receive dietary and ketone monitoring education.
Assessments and monitoring undertaken at each consultation include anthropometry, biochemistry, compliance, tolerance, acceptability, quality of life and ketosis.
Informed consent will be obtained prior to enrollment and the patient may withdraw at any time.
An information study is also embedded into KEATING, to aid understanding of the patients' recruitment experience and viewpoints, by interviewing a sub-sample of patients and their relatives/ carers. This will enable the design of bespoke strategies to optimise recruitment to future trials related to ketogenic diets and gliomas
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glioblastoma, Glioblastoma Multiforme, Glioblastoma, Adult
Keywords
ketogenic
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
MKD and MCT ketogenic diets
Masking
None (Open Label)
Allocation
Randomized
Enrollment
12 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Modified ketogenic diet (MKD)
Arm Type
Active Comparator
Arm Description
MKD: 80% fat and 5% carbohydrate (% of total energy requirements per day).
Arm Title
Medium chain triglyceride (MCT) diet
Arm Type
Active Comparator
Arm Description
MCT: 75% fat (30% of which is medium chain fatty acids taken as a supplement) and 5% carbohydrate (% of total energy requirements per day).
Intervention Type
Other
Intervention Name(s)
MKD
Intervention Description
Modified ketogenic diet
Intervention Type
Other
Intervention Name(s)
MCT
Intervention Description
Medium chain triglyceride ketogenic diet
Primary Outcome Measure Information:
Title
To assess retention and drop out rates
Description
Number of patients who start randomized treatment as a proportion of the number randomized ;
Time Frame
12 weeks
Title
To assess retention and drop out rates
Description
The number of patients who complete 12 weeks as a proportion of the number randomized
Time Frame
12 weeks
Title
To assess retention and drop out rates
Description
Description of barriers and facilitators to data collection and participant retention
Time Frame
12 weeks
Title
To assess retention and drop out rates
Description
The time to dietary discontinuation
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Estimation of recruitment rates
Description
Actual recruitment compared to proposed recruitment
Time Frame
12 months
Title
Enrollment of patients
Description
Number of patients initiated on diet prior to starting oncological treatments.
Time Frame
12 months
Title
Enrollment of patients
Description
Number of patients initiated on diet during oncological treatments.
Time Frame
12 months
Title
Enrollment of patients
Description
Number of patients initiated on diet post oncological treatments.
Time Frame
12 months
Title
Long term retention
Description
Time to dietary discontinuation after week 12
Time Frame
2 years
Title
Dietary adjustments required to achieve ketosis
Description
Number of dietary adjustments to macronutrient composition of MCT and MKD diets required to achieve ketosis.
Time Frame
2 years
Title
Self reported dietary compliance
Description
Self reported by compliance rate
Time Frame
2 years
Title
Calculated dietary compliance
Description
Analysed by comparing macronutrient content assessed via 3 day food diaries to advised macronutrient content.
Time Frame
2 years
Title
MCT compliance
Description
Dose of MCT taken compared to dose advised.
Time Frame
2 years
Title
Ketosis levels
Description
Self reported urinary ketone levels twice daily for first 6 weeks then once per week thereafter and blood ketone and glucose levels weekly.
Time Frame
2 years
Title
Dietetic time required for interventions
Description
Dietetic time spent on clinical and non clinical activities relating to the trial.
Time Frame
2 years
Title
Protocol refinements required
Description
Number of deviations from the protocol including reasons for deviations.
Time Frame
2 years
Title
Sample size estimates for future trials
Description
Number of participants required for future phase III clinical trials
Time Frame
2 years
Title
Quality of life
Description
Change in quality of life assessed through EORTC QLQ C30 and BN 20 questionnaires
Time Frame
2 years
Title
Food acceptability
Description
Change in food acceptability assessed through food acceptability questionnaire
Time Frame
2 years
Title
Gastrointestinal side effects
Description
Number of reported gastrointestinal side effects assessed through EORTC QLQ C30 questionnaire and Common Terminology Criteria for Adverse Events.
Time Frame
2 years
Title
Changes to biochemical markers
Description
Changes to biochemical markers (renal, bone, LFT, lipid profiles) during the duration of the diet.
Time Frame
2 years
Title
Anthropometric changes
Description
Changes to anthropometry (weight, body mass index, fat mass, muscle circumference, hand grip strength) during the duration of the diet.
Time Frame
2 years
Title
Completeness of data
Description
Number of complete data sets for all trial outcomes
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age ≥16 years
Patient at The Walton Centre NHS Foundation Trust
Performance status ≤2
Confirmed histological diagnosis of glioblastoma
Undergone surgical resection or biopsy and will go onto receive/ is receiving/ has received oncological treatments
Exclusion Criteria:
Having prior use of KD
Kidney dysfunction
Liver dysfunction
Gall bladder dysfunction
Metabolic disorder
Eating disorder
Diabetes (requiring medication)
Body mass index ≤ 18.5kg/m2
Weight loss medications
Currently pregnant or breast feeding
Performance status ≥3
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael D Jenkinson, PhD, FRCS
Organizational Affiliation
University of Liverpool
Official's Role
Principal Investigator
Facility Information:
Facility Name
Univeristy of Liverpool/ The Walton Centre NHS Foundation Trust
City
Liverpool
State/Province
Merseyside
ZIP/Postal Code
L9 7LJ
Country
United Kingdom
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
29209515
Citation
Martin-McGill KJ, Marson AG, Tudur Smith C, Jenkinson MD. Ketogenic diets as an adjuvant therapy in glioblastoma (the KEATING trial): study protocol for a randomised pilot study. Pilot Feasibility Stud. 2017 Nov 28;3:67. doi: 10.1186/s40814-017-0209-9. eCollection 2017.
Results Reference
derived
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Ketogenic Diets as an Adjuvant Therapy in Glioblastoma
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