Pioglitazone Hydrochloride in Preventing Radiation-Induced Cognitive Dysfunction in Treating Patients With Brain Tumors

Pioglitazone Hydrochloride in Preventing Radiation-Induced Cognitive Dysfunction in Treating Patients With Brain Tumors
This study is currently recruiting participants.
Verified September 2010 by Wake Forest University

First Received on June 25, 2010.  
Last Updated on December 9, 2010  
History of Changes
Sponsor: Wake Forest University
Information provided by: Wake Forest University
ClinicalTrials.gov Identifier: NCT01151670

RATIONALE: Pioglitazone hydrochloride may be effective treatment for cognitive dysfunction caused by radiation therapy.

PURPOSE: This phase I trial is studying the side effects and best dose of pioglitazone hydrochloride in preventing radiation-induced cognitive dysfunction in treating patients with brain tumors.

Condition Intervention Phase
Brain Neoplasms, Malignant
Brain Neoplasms, Benign
Malignant Meningioma
Glioblastoma Multiforme
Anaplastic Astrocytoma
Drug: pioglitazone
Drug: Pioglitazone
Phase 1

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Supportive Care
Official Title: Use of Pioglitazone for the Prevention of Radiation-Induced Cognitive Dysfunction

Resource links provided by NLM:

Further study details as provided by Wake Forest University:

Primary Outcome Measures:

  • Best tolerated dose of 2 different doses of orally administered pioglitazone [ Time Frame: From first dose to 1 day after last dose of drug ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:

  • Toxicities associated with both dose levels [ Time Frame: From first dose to 1 day after last dose of drug ] [ Designated as safety issue: Yes ]
  • To evaluate the effect of pioglitazone on glycemic levels and hemoglobin A1c values when pioglitazone is used as a cytoprotective agent concurrent with radiotherapy in normoglycemic patients. [ Time Frame: From first dose to 1 day after last dose of drug ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 100
Study Start Date: August 2010
Estimated Study Completion Date: August 2013
Estimated Primary Completion Date: August 2012 (Final data collection date for primary outcome measure)


Assigned Interventions
Experimental: Arm I

Pioglitazone 22.5 mg once daily by mouth
Drug: pioglitazone

Pioglitazone 22.5 mg daily before, during and after radiation therapy.
Other Names:
  • Actos
  • pioglitazone
Experimental: Arm 2

Pioglitazone 45 mg once daily by mouth
Drug: Pioglitazone

Pioglitazone 45 mg by mouth daily before, during and after radiation therapy
Other Name: Actos

Detailed Description:


I. To evaluate the tolerability and toxicity associated with two different dose regimens of pioglitazone administered orally as a cytoprotective agent against radiation-induced brain injury.


I. To evaluate the effect of pioglitazone on glycemic levels and hemoglobin A1c values when pioglitazone is used as a cytoprotective agent concurrent with radiotherapy in normoglycemic patients.

OUTLINE: Patients undergo fractionated external beam radiotherapy, 3-D conformal radiotherapy, or intensity-modulated radiotherapy. Patients receive oral pioglitazone hydrochloride once daily before for 1 week prior to brain irradiation, during and and continuing for 6 months after completion of radiation radiotherapy. After completion of study treatment, patients are followed periodically.


Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Patients must have histologically or cytologically confirmed brain tumors of the following types: Group 1: malignant brain tumors (glioblastoma multiforme, anaplastic gliomas, brain metastases, and other malignant brain tumors); or Group 2: low grade brain tumors (low grade gliomas, meningiomas, and other low grade brain tumors)
  • All stages and grades of brain tumors are eligible
  • Patients must have an ECOG performance status of 0-2
  • Patients must have agreed to be treated with fractionated, external beam radiation treatment (EBRT) with either curative or palliative intent (the length of the radiation course must at least be ten fractions)
  • Patients must have agreed to have CT and MR imaging for purposes of radiation treatment planning, radiation treatment monitoring, and/or radiation treatment evaluation
  • Patients must have measurable disease and/or relevant anatomic features using Magnetic Resonance Imaging
  • Prior therapies (cytotoxic, surgery, and radiation) are acceptable
  • Use of steroids is acceptable when indicated
  • Patients must be able to understand and willingly give informed written consent to participate
  • Women of childbearing potential must not be pregnant or nursing and must use medically appropriate contraception if sexually active
  • Patients must have a life expectancy of greater than 3 months
  • Patients must be willing to comply with an oral treatment regimen and be able to swallow oral study tablets

Exclusion Criteria:

  • History of allergic reactions to pioglitazone or any other member of the thiazolidinedione family
  • Current diagnosis of diabetes as defined by fasting blood sugar > 125, treatment with anti-diabetic medications, or history of diabetes
  • Patients who take insulin
  • Patients who have NYHA class III or IV heart failure
  • Patients who have elevated transaminases (AST or ALT > 2.5 times normal limit)
  • Patients who have significantly impaired renal function (creatinine >= 1.5)
  • Patients who are significantly anemic (hematocrit < 33% in men, or < 30% in women)
  • Patients who have symptomatic edema (>= grade 2)
  • Patients who are on medications that have been shown to have a drug interaction with pioglitazone: atorvastatin (doses > 80 mg/day), systemic anti-fungals, medications with significant CYP 3A4 inhibiting properties
  • 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
  • Pregnant women are excluded from this study if their pregnancy precludes radiation treatment because ionizing radiation used in radiation treatment is an agent with known potential for teratogenic or abortifacient effects
  • Patients with psychiatric or social illnesses that may impair compliance with the trial requirements
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT01151670

United States, North Carolina
Wake Forest University Health Sciences Recruiting
Winston-Salem, North Carolina, United States, 27157
Contact: Michael D. Chan     336-716-1656     mchan@wfubmc.edu    
Principal Investigator: Michael D. Chan            
Sponsors and Collaborators
Wake Forest University
Principal Investigator: Michael Chan Wake Forest University
  More Information

No publications provided

Responsible Party: Chan, Michael, Wake Forest University Health Sciences
ClinicalTrials.gov Identifier: NCT01151670    
History of Changes
Other Study ID Numbers: CCCWFU 97409, NCI-2009-01452
Study First Received: June 25, 2010
Last Updated: December 9, 2010
Health Authority: United States: Institutional Review Board

Keywords provided by Wake Forest University:

radiation therapy
cognitive dysfunction
brain tumor
memory problems
short term memory loss

Additional relevant MeSH terms:

Brain Neoplasms
Cognition Disorders
Neoplasms, Neuroepithelial
Neuroectodermal Tumors
Neoplasms, Germ Cell and Embryonal
Neoplasms by Histologic Type
Neoplasms, Glandular and Epithelial
Neoplasms, Nerve Tissue
Central Nervous System Neoplasms
Nervous System Neoplasms
Neoplasms by Site
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Neoplasms, Vascular Tissue
Meningeal Neoplasms
Delirium, Dementia, Amnestic, Cognitive Disorders
Mental Disorders
Hypoglycemic Agents
Physiological Effects of Drugs
Pharmacologic Actions

ClinicalTrials.gov processed this record on August 21, 2012

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