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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
Tufts Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Glioma focused on measuring Glioma, KetoPhyt, High-grade gliomas

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept 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

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

First Posted
April 26, 2022
Last Updated
August 24, 2023
Sponsor
Tufts Medical Center
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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

Citations:
PubMed Identifier
22563484
Citation
Abdelwahab MG, Fenton KE, Preul MC, Rho JM, Lynch A, Stafford P, Scheck AC. The ketogenic diet is an effective adjuvant to radiation therapy for the treatment of malignant glioma. PLoS One. 2012;7(5):e36197. doi: 10.1371/journal.pone.0036197. Epub 2012 May 1.
Results Reference
background
PubMed Identifier
24835084
Citation
Candelario KM, Steindler DA. The role of extracellular vesicles in the progression of neurodegenerative disease and cancer. Trends Mol Med. 2014 Jul;20(7):368-74. doi: 10.1016/j.molmed.2014.04.003. Epub 2014 May 14.
Results Reference
background
PubMed Identifier
31743443
Citation
Candelario KM, Balaj L, Zheng T, Skog J, Scheffler B, Breakefield X, Schule B, Steindler DA. Exosome/microvesicle content is altered in leucine-rich repeat kinase 2 mutant induced pluripotent stem cell-derived neural cells. J Comp Neurol. 2020 May;528(7):1203-1215. doi: 10.1002/cne.24819. Epub 2019 Nov 30.
Results Reference
background
PubMed Identifier
24442482
Citation
Champ CE, Palmer JD, Volek JS, Werner-Wasik M, Andrews DW, Evans JJ, Glass J, Kim L, Shi W. Targeting metabolism with a ketogenic diet during the treatment of glioblastoma multiforme. J Neurooncol. 2014 Mar;117(1):125-31. doi: 10.1007/s11060-014-1362-0. Epub 2014 Jan 19.
Results Reference
background
PubMed Identifier
24558975
Citation
Fadrosh DW, Ma B, Gajer P, Sengamalay N, Ott S, Brotman RM, Ravel J. An improved dual-indexing approach for multiplexed 16S rRNA gene sequencing on the Illumina MiSeq platform. Microbiome. 2014 Feb 24;2(1):6. doi: 10.1186/2049-2618-2-6.
Results Reference
background
PubMed Identifier
25355830
Citation
Klein P, Tyrlikova I, Mathews GC. Dietary treatment in adults with refractory epilepsy: a review. Neurology. 2014 Nov 18;83(21):1978-85. doi: 10.1212/WNL.0000000000001004. Epub 2014 Oct 29.
Results Reference
background
PubMed Identifier
19066529
Citation
Liu L, Duff K. A technique for serial collection of cerebrospinal fluid from the cisterna magna in mouse. J Vis Exp. 2008 Nov 10;(21):960. doi: 10.3791/960.
Results Reference
background
PubMed Identifier
26631612
Citation
Martuscello RT, Vedam-Mai V, McCarthy DJ, Schmoll ME, Jundi MA, Louviere CD, Griffith BG, Skinner CL, Suslov O, Deleyrolle LP, Reynolds BA. A Supplemented High-Fat Low-Carbohydrate Diet for the Treatment of Glioblastoma. Clin Cancer Res. 2016 May 15;22(10):2482-95. doi: 10.1158/1078-0432.CCR-15-0916. Epub 2015 Dec 2.
Results Reference
background
PubMed Identifier
25798181
Citation
Meidenbauer JJ, Mukherjee P, Seyfried TN. The glucose ketone index calculator: a simple tool to monitor therapeutic efficacy for metabolic management of brain cancer. Nutr Metab (Lond). 2015 Mar 11;12:12. doi: 10.1186/s12986-015-0009-2. eCollection 2015.
Results Reference
background
PubMed Identifier
25806103
Citation
Schwartz K, Chang HT, Nikolai M, Pernicone J, Rhee S, Olson K, Kurniali PC, Hord NG, Noel M. Treatment of glioma patients with ketogenic diets: report of two cases treated with an IRB-approved energy-restricted ketogenic diet protocol and review of the literature. Cancer Metab. 2015 Mar 25;3:3. doi: 10.1186/s40170-015-0129-1. eCollection 2015.
Results Reference
background
PubMed Identifier
31347659
Citation
Sherrier M, Li H. The impact of keto-adaptation on exercise performance and the role of metabolic-regulating cytokines. Am J Clin Nutr. 2019 Sep 1;110(3):562-573. doi: 10.1093/ajcn/nqz145.
Results Reference
background
PubMed Identifier
21351156
Citation
Siebzehnrubl FA, Reynolds BA, Vescovi A, Steindler DA, Deleyrolle LP. The origins of glioma: E Pluribus Unum? Glia. 2011 Aug;59(8):1135-47. doi: 10.1002/glia.21143. Epub 2011 Feb 23.
Results Reference
background
PubMed Identifier
23818228
Citation
Siebzehnrubl FA, Silver DJ, Tugertimur B, Deleyrolle LP, Siebzehnrubl D, Sarkisian MR, Devers KG, Yachnis AT, Kupper MD, Neal D, Nabilsi NH, Kladde MP, Suslov O, Brabletz S, Brabletz T, Reynolds BA, Steindler DA. The ZEB1 pathway links glioblastoma initiation, invasion and chemoresistance. EMBO Mol Med. 2013 Aug;5(8):1196-212. doi: 10.1002/emmm.201302827. Epub 2013 Jul 1.
Results Reference
background
PubMed Identifier
19011622
Citation
Skog J, Wurdinger T, van Rijn S, Meijer DH, Gainche L, Sena-Esteves M, Curry WT Jr, Carter BS, Krichevsky AM, Breakefield XO. Glioblastoma microvesicles transport RNA and proteins that promote tumour growth and provide diagnostic biomarkers. Nat Cell Biol. 2008 Dec;10(12):1470-6. doi: 10.1038/ncb1800. Epub 2008 Nov 16.
Results Reference
background
PubMed Identifier
26649186
Citation
Strowd RE, Cervenka MC, Henry BJ, Kossoff EH, Hartman AL, Blakeley JO. Glycemic modulation in neuro-oncology: experience and future directions using a modified Atkins diet for high-grade brain tumors. Neurooncol Pract. 2015 Sep;2(3):127-136. doi: 10.1093/nop/npv010. Epub 2015 May 26.
Results Reference
background
PubMed Identifier
19269895
Citation
Stupp R, Hegi ME, Mason WP, van den Bent MJ, Taphoorn MJ, Janzer RC, Ludwin SK, Allgeier A, Fisher B, Belanger K, Hau P, Brandes AA, Gijtenbeek J, Marosi C, Vecht CJ, Mokhtari K, Wesseling P, Villa S, Eisenhauer E, Gorlia T, Weller M, Lacombe D, Cairncross JG, Mirimanoff RO; European Organisation for Research and Treatment of Cancer Brain Tumour and Radiation Oncology Groups; National Cancer Institute of Canada Clinical Trials Group. Effects of radiotherapy with concomitant and adjuvant temozolomide versus radiotherapy alone on survival in glioblastoma in a randomised phase III study: 5-year analysis of the EORTC-NCIC trial. Lancet Oncol. 2009 May;10(5):459-66. doi: 10.1016/S1470-2045(09)70025-7. Epub 2009 Mar 9.
Results Reference
background
PubMed Identifier
29260225
Citation
Stupp R, Taillibert S, Kanner A, Read W, Steinberg D, Lhermitte B, Toms S, Idbaih A, Ahluwalia MS, Fink K, Di Meco F, Lieberman F, Zhu JJ, Stragliotto G, Tran D, Brem S, Hottinger A, Kirson ED, Lavy-Shahaf G, Weinberg U, Kim CY, Paek SH, Nicholas G, Bruna J, Hirte H, Weller M, Palti Y, Hegi ME, Ram Z. Effect of Tumor-Treating Fields Plus Maintenance Temozolomide vs Maintenance Temozolomide Alone on Survival in Patients With Glioblastoma: A Randomized Clinical Trial. JAMA. 2017 Dec 19;318(23):2306-2316. doi: 10.1001/jama.2017.18718. Erratum In: JAMA. 2018 May 1;319(17):1824.
Results Reference
background
PubMed Identifier
26345506
Citation
Suslov O, Silver DJ, Siebzehnrubl FA, Orjalo A, Ptitsyn A, Steindler DA. Application of an RNA amplification method for reliable single-cell transcriptome analysis. Biotechniques. 2015 Sep 1;59(3):137-48. doi: 10.2144/000114331. eCollection 2015 Sep.
Results Reference
background
PubMed Identifier
18228490
Citation
Thery C, Amigorena S, Raposo G, Clayton A. Isolation and characterization of exosomes from cell culture supernatants and biological fluids. Curr Protoc Cell Biol. 2006 Apr;Chapter 3:Unit 3.22. doi: 10.1002/0471143030.cb0322s30.
Results Reference
background
PubMed Identifier
26418763
Citation
Truong DT, Franzosa EA, Tickle TL, Scholz M, Weingart G, Pasolli E, Tett A, Huttenhower C, Segata N. MetaPhlAn2 for enhanced metagenomic taxonomic profiling. Nat Methods. 2015 Oct;12(10):902-3. doi: 10.1038/nmeth.3589. No abstract available. Erratum In: Nat Methods. 2016 Jan;13(1):101.
Results Reference
background
PubMed Identifier
22503788
Citation
Vlassov AV, Magdaleno S, Setterquist R, Conrad R. Exosomes: current knowledge of their composition, biological functions, and diagnostic and therapeutic potentials. Biochim Biophys Acta. 2012 Jul;1820(7):940-8. doi: 10.1016/j.bbagen.2012.03.017. Epub 2012 Apr 1.
Results Reference
background
PubMed Identifier
28325264
Citation
Winter SF, Loebel F, Dietrich J. Role of ketogenic metabolic therapy in malignant glioma: A systematic review. Crit Rev Oncol Hematol. 2017 Apr;112:41-58. doi: 10.1016/j.critrevonc.2017.02.016. Epub 2017 Feb 20.
Results Reference
background
PubMed Identifier
24503133
Citation
Woolf EC, Scheck AC. The ketogenic diet for the treatment of malignant glioma. J Lipid Res. 2015 Jan;56(1):5-10. doi: 10.1194/jlr.R046797. Epub 2014 Feb 6.
Results Reference
background
PubMed Identifier
26590418
Citation
Zeevi D, Korem T, Zmora N, Israeli D, Rothschild D, Weinberger A, Ben-Yacov O, Lador D, Avnit-Sagi T, Lotan-Pompan M, Suez J, Mahdi JA, Matot E, Malka G, Kosower N, Rein M, Zilberman-Schapira G, Dohnalova L, Pevsner-Fischer M, Bikovsky R, Halpern Z, Elinav E, Segal E. Personalized Nutrition by Prediction of Glycemic Responses. Cell. 2015 Nov 19;163(5):1079-1094. doi: 10.1016/j.cell.2015.11.001.
Results Reference
background

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The KetoGlioma (Ketogenic Glioma) Study

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