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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02046187
Other study ID # KD-13BN069
Secondary ID
Status Terminated
Phase Phase 1/Phase 2
First received
Last updated
Start date October 2013
Est. completion date February 2017

Study information

Verified date June 2021
Source St. Joseph's Hospital and Medical Center, Phoenix
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to see if reducing blood sugar and increasing ketones (a metabolic product that comes from using fats for energy) can increase survival and enhance the the effects of standard radiation and chemotherapy treatments used to treat glioblastoma multiforme (GBM). These changes occur from use of a ketogenic diet. This research has 2 goals: 1. Show that patients can tolerate the diet and maintain low blood glucose and high blood ketone levels. 2. Show if this diet enhances the effectiveness of standard treatment by prolonging survival of patients with a GBM.


Description:

The investigators propose to offer this study to patients with newly diagnosed glioblastoma multiforme (GBM) that undergo gross total resection (GTR) or subtotal resection (STR) of their tumor. Post-operatively, these patients and their families will be instructed in the implementation of the Ketogenic Diet (KD) and it will be started as soon as possible following surgery to achieve ketosis and reduction of blood sugar. Patients will receive standard chemoradiotherapy with fractionated external beam radiation (60Gy) and concurrent oral temozolomide chemotherapy followed by 12 adjuvant cycles of temozolomide chemotherapy on a standard dose schedule. Outcome measures of the study group will be compared to historic controls in the treatment arm from the European Organization for Research and Treatment of Cancer (EORTC) temozolomide study published by Roger Stupp et al, New England Journal of Medicine, March 10, 2005. Note: Gross Total Resection (GTR), Subtotal Resection (STR), temozolomide (Temodar), and radiation therapy are routine care for GBM and are not an investigational component of this study. Study end-points: Primary: Ketogenic diet (KD) tolerance and compliance in brain tumor patients. The diet will be considered tolerable if the patient chooses to remain compliant. Compliance is monitored by the dietician using self reporting of diet, blood glucose and blood ketone levels. Secondary: Overall survival, time to recurrence, health and therapy-related quality of life. Overall survival and progression free survival will be measured and compared to the historic controls who received chemoradiotherapy in standard dose scheduling. Laboratory correlate: Molecular/immunohistochemical analysis of tumors that do and do not respond to a KD.


Recruitment information / eligibility

Status Terminated
Enrollment 14
Est. completion date February 2017
Est. primary completion date February 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - adult patients, 18 - 80 years of age, - a single enhancing lesion of the brain with MRI appearance consistent with GBM - Pathologic confirmation of GBM - Zubrod Performance Scale (ZPS) < 2 - Must be able to undergo MRI imaging with gadolinium - Must have access to a computer and the internet (to use KetoCalculatorĀ© on-line Database) Exclusion Criteria: - unable to undergo MRI with gadolinium - genetic disorders of fat metabolism - patients receiving sodium valproate (may cause false ketone reading in urine) - diabetes - enrolled in another treatment trial for GBM

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Ketogenic Diet
Patients/families meet with the study dietician after surgery to discuss the ketogenic diet (KD), ask questions and plan clinic visits. Before radiation and chemotherapy begins, training takes place about the diet, meal planning and ketone/glucose monitoring. Ketosis will begin with the help of the dietitian one week before radiation begins. The patient will follow a classic 4/1 KD during chemo-radiation, followed by a modified Atkins diet during monthly chemotherapy. At the end of this period patients will follow a normal low carbohydrate diet similar to a Diabetic diet. The dietitian will follow the patient over the course of treatment. The patient will take and record ketone and glucose blood levels daily from start to end of treatment MRI scan, and meet with the dietitian weekly during radiation, at follow-up visits and on an as-needed basis.
Radiation:
Radiation therapy
Patients receive standard dose (60Gy/30 fractions) external beam radiation
Drug:
Temozolomide
patients receive standard dose (75 mg/kg/day) temozolomide by mouth daily with radiation for 6 weeks. patients will also have standard maintenance dose (150-200 mg/kg/day) for five days each month for 12 cycles following radiation course.

Locations

Country Name City State
United States Barrow Neurological Institute at St. Joseph's Hospital and Medical Center Phoenix Arizona

Sponsors (1)

Lead Sponsor Collaborator
St. Joseph's Hospital and Medical Center, Phoenix

Country where clinical trial is conducted

United States, 

References & Publications (3)

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. — View Citation

Scheck AC, Abdelwahab MG, Fenton KE, Stafford P. The ketogenic diet for the treatment of glioma: insights from genetic profiling. Epilepsy Res. 2012 Jul;100(3):327-37. doi: 10.1016/j.eplepsyres.2011.09.022. Epub 2011 Oct 22. Review. — View Citation

Stafford P, Abdelwahab MG, Kim DY, Preul MC, Rho JM, Scheck AC. The ketogenic diet reverses gene expression patterns and reduces reactive oxygen species levels when used as an adjuvant therapy for glioma. Nutr Metab (Lond). 2010 Sep 10;7:74. doi: 10.1186/1743-7075-7-74. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Number of participants with adverse events Number of participants with adverse events from initiation of ketogenic diet through end of radiation (while on ketogenic diet) 8 weeks
Secondary overall survival overall survival 2 years
Secondary time to progression time to progression 2 years
Secondary quality of life patient reported outcome of their quality of life using FACT-BR (version 4) survey 2 years
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