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Clinical Trials/NCT04461938
NCT04461938
Active, not recruiting
Not Applicable

Characterization of Metabolic Changes in the Glioma Tumor Tissue Induced by Transient Fasting (ERGO3)

Goethe University1 site in 1 country30 target enrollmentAugust 19, 2020
ConditionsGlioma, Mixed

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Glioma, Mixed
Sponsor
Goethe University
Enrollment
30
Locations
1
Primary Endpoint
Immunological changes
Status
Active, not recruiting
Last Updated
last year

Overview

Brief Summary

Nutritional interventions such as ketogenic diet (KD) or fasting are currently under evaluation as anti-cancer treatment. In glioma patient cohorts, the feasibility and safety of fasting in addition to antitumor treatment has been shown. However, it is still unclear whether fasting exerts effects on the glioma tumor tissue at all, and whether fasting causes metabolic or immunological changes in the glioma microenvironment that could be exploited therapeutically. Therefore, the central contribution of this study is to characterize metabolic and immunological changes in the glioma tumor tissue induced by a fasting cycle of 72 hours prior to biopsy or resection.

Registry
clinicaltrials.gov
Start Date
August 19, 2020
End Date
June 30, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Goethe University
Responsible Party
Principal Investigator
Principal Investigator

Michael Ronellenfitsch

Princial Investigator

Goethe University

Eligibility Criteria

Inclusion Criteria

  • suspicion of glioma World Health Organization (WHO) grade II, III or IV as assessed by cerebral imaging (MRI)
  • MRI-suspected relapse of previously diagnosed glioma
  • interdisciplinary recommendation for resection or biopsy
  • karnofsky performance status \>= 60, Eastern Cooperative Oncology Group Performance Status (ECOG) \<= 2
  • creatinine \<= 2,0 mg/dl, urea \<= 100 mg/dl
  • alanine aminotransferase (ALAT), alanine aminotransferase aspartate transaminase (ASAT) \<= 7x upper normal limit
  • international normalized ratio (INR) ≤ 1,5, thrombocytes \> 100000/µl, leukocytes \> 3000/µl

Exclusion Criteria

  • bowel obstruction, subileus
  • insulin-dependent diabetes
  • dexamethasone \>4mg/day
  • decompensated heart failure (NYHA \> 2)
  • myocardial infarction within the last 6 months, symptomatic atrial fibrillation
  • severe acute infection or clinically relevant immunosuppression (HIV infection, granulocytopenia \<1000/ µl, lymphocytopenia \<500/ µl
  • malnutrition, cachexia (BMI \<18)
  • other medical conditions that might increase the risk of the dietary intervention
  • pregnancy
  • uncontrolled thyroid function

Outcomes

Primary Outcomes

Immunological changes

Time Frame: 5 days

Flow cytometry including T- and B-lymphocytes natural killer (NK) cells in blood samples. Analysis of gut microbiome prior to and following fasting.

General metabolic changes

Time Frame: 5 days

Main target parameters of MR spectroscopic imaging are detection of intracerebral ketone bodies (acetone, acetoacetate, beta-hydroxybutyrate), changes in lactate and adenosine triphosphate / adenosine diphosphate (ATP/ADP) concentrations and changes in intracellular pH (pHi) as determined from the chemical shift difference between inorganic phosphate (Pi) and phosphocreatine (PCr). Tumor tissue and healthy appearing normal white matter of the contralateral hemisphere will be examined. Tumor tissue will be analysed by metabolome and proteome analysis and RNA sequencing. Patient serum will be analysed by proteome analysis.

Alterations in electric brain activity

Time Frame: 5 days

Non-invasive electroencephalography (EEG) will be performed prior to and following fasting. It will be assessed with regard to chief frequencies and the presence of epilepsy-associated manifestations (e.g. epileptiform discharges, seizures).

Changes in metabolism - induction of ketosis

Time Frame: 5 days

The presence of ketone bodies in patient blood will be assessed by capillary sampling from a finger or an ear lobe. The presence of ketone bodies in urine will be assessed by urine test strips.

Secondary Outcomes

  • Assessment to measure the tolerability of the diet by questionnaire(5 days)
  • Intake of fluids and calories reported by dietary diary(5 days)

Study Sites (1)

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