Ketogenic Diet With Chemoradiation for Lung Cancer (KETOLUNG)

Carcinoma, Non-Small-Cell Lung Clinical Trial

Official title:

A Phase I Trial of a Ketogenic Diet With Concurrent Chemoradiation for Non-small Cell Lung Cancer

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01419587
• Other study ID #: 201102773
• Secondary ID: 1R21CA161182
• Status: Terminated
• Phase: N/A
• First received: July 29, 2011
• Last updated: January 4, 2018
• Start date: July 2011
• Est. completion date: July 11, 2017

Study information

• Verified date: January 2018
• Source: University of Iowa
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study investigates if using a very low carbohydrate diet during combined chemotherapy and radiation therapy is safe and if it can be tolerated by lung cancer patients.

Description:

Standard treatment for lung cancer includes chemotherapy concurrent with radiation therapy (chemoradiation).

This study is a phase I trial to determine the safety of dietary manipulation during chemoradiation for lung cancer. Specifically, pre-clinical data from mouse studies indicates a ketogenic diet increases tumor cell killing.

Participants will:

• Utilize a specialized ketogenic diet designed by bionutritional services of the clinical research unit. This diet begins 2 days before chemoradiation and continues through at least 5 weeks of chemoradiation.

• Have blood drawn for research purposes weekly to determine measurements of oxidative stress

• Have urine collected sporadically through the study to determine measurements of oxidative stress

• Keep a diary of concomitant medications, side effects, and blood sugars

• Have follow-up to monitor for outcomes and overall survival

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 11
• Est. completion date: July 11, 2017
• Est. primary completion date: June 30, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically or cytologically documented NSCLC.

• Candidate for primary chemoradiation as decided by both medical and radiation oncology.

• Cancer should be staged via AJCC as IIIA or IIIB.

• Stage IV patients are considered provided they have a single non-CNS metastasis (that is amenable to treatment with radiation therapy).

• Age = 18 years

• ECOG performance status 0-2 (Karnofsky > 50%, see Appendix A).

• Hypertensive medication should be initiated or increased for optimal blood pressure control according to standard public health guidelines prior to starting the ketogenic diet.

• Patients must have normal organ and marrow function as defined below:

• leukocytes = 3,000/mm3

• absolute neutrophil count = 1,500/mm3

• platelets = 100,000/mm3

• total bilirubin < 1.5 mg/dl

• Hgb A1C < or = to 8%

• AST(SGOT) < or = to 2 X institutional upper limit of normal

• creatinine < 1.5 X institutional upper limit of normal OR creatinine clearance = 60 mL/min/1.73 m2 for patients with creatinine levels above institutional normal.

• Not pregnant. Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.

• Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:

• Life expectancy of 3 or less months.

• Prior thoracic radiotherapy.

• Prior therapy, with the intent to treat, the current diagnosis of lung cancer.

• Known G6PD (glucose-6-phosphate dehydrogenase) deficiency.

• Systemic corticosteroids for any reason (inhaled corticosteroids are allowed).

• Other investigational agents/therapy with the intention to treat the disease under study (observational or imaging trials are acceptable).

• Uncontrolled diabetes defined as a hemoglobin A1C level > 8% (therapeutic action is indicated at greater than 8%).

• Diabetes is not exclusionary provided the patient is not maintained with either oral medications or insulin.

• Uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements as determined by study team members.

• Pregnant or lactating women: The risks of radiation and chemotherapy to a fetus are well documented.

Female and male patients of all ethnic groups will be eligible for treatment in these protocols.

Related Conditions & MeSH terms

• Carcinoma, Non-Small-Cell Lung
• Lung Neoplasms

Intervention

Dietary Supplement:
• Ketogenic diet
A ketogenic diet matching the fat to carbohydrate + proteins in Keto-Cal(R) 4:1 by Nutricia North America.

Locations

Country	Name	City	State
United States	Holden Comprehensive Cancer Center	Iowa City	Iowa

Sponsors (4)

Lead Sponsor	Collaborator
University of Iowa	National Cancer Institute (NCI), National Institutes of Health (NIH), Nutricia North America

Country where clinical trial is conducted

United States, 

References & Publications (1)

Zahra A, Fath MA, Opat E, Mapuskar KA, Bhatia SK, Ma DC, Rodman SN III, Snyders TP, Chenard CA, Eichenberger-Gilmore JM, Bodeker KL, Ahmann L, Smith BJ, Vollstedt SA, Brown HA, Hejleh TA, Clamon GH, Berg DJ, Szweda LI, Spitz DR, Buatti JM, Allen BG. Consu — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Frequency of Adverse Events (Safety)	Categorize and quantify adverse events in subjects implementing a ketogenic diet while undergoing definitive chemoradiation therapy.	Weekly for 8 weeks
Secondary	Ketone levels	Quantify blood ketone levels via both finger-stick prior to daily radiation therapy and weekly lab analysis while on a ketogenic diet. Radiation is administered Monday through Friday only.	Daily during treatment for 6 weeks
Secondary	Blood glucose levels	Quantify blood glucose levels via finger-stick prior to daily radiation therapy while on a ketogenic diet. Radiation therapy is administered Monday through Friday only.	Daily during treatment for 6 weeks
Secondary	Oxidative stress parameters	Determine oxidative stress parameters in plasma and urine samples during the course of treatment.	Weeks 1, 2, 3, 4, 5, and 6 of treatment and at 1 month follow-up
Secondary	Progression Free Survival (months)	From date of treatment until the first date of documented progression or date of death, whichever comes first, assessed no less than every 12 months for the first 60 months post-therapy.	Every 12 months for 60 months