A Multi-modality Imaging Assessment of Chemobrain

This study is currently recruiting participants. (see Contacts and Locations)
Verified July 2014 by University of Utah
Sponsor:
Information provided by (Responsible Party):
University of Utah
ClinicalTrials.gov Identifier:
NCT00708045
First received: June 27, 2008
Last updated: July 28, 2014
Last verified: July 2014
  Purpose

Patients must have had their breast cancer treated at the Huntsman Cancer Institute to be eligible for this trial.

OBJECTIVES:

To use quantitative FDG-PET, functional MRI (fMRI) and co-registered anatomic MRI imaging to better understand the cognitive disorder known as "chemobrain" which effects up to 16 -50% of individuals receiving long-term adjuvant chemotherapy [Tannock 2004, Matsuda 2005]. The study is exploratory to obtain proof of feasibility pilot data to support an eventual submission to the NIH.

Neuropsychological Testing A battery of testing will be used to assess the subjective complaints of cognitive impairment in the symptomatic patient cohort. Similarly the same battery of tests will be used to assure that the non-symptomatic patient control group and the age-matched normal controls do not exhibit any cognitive impairment. The following set of clinical tests will be performed to assess the degree of cognitive impairment in all subjects.


Condition Intervention
Cancer
Procedure: Imaging assessments

Study Type: Interventional
Study Design: Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Diagnostic
Official Title: A Multi-modality Imaging Assessment of Chemobrain

Resource links provided by NLM:


Further study details as provided by University of Utah:

Primary Outcome Measures:
  • To use quantitative FDG-PET, functional MRI (fMRI) and co-registered anatomic MRI imaging to better understand the cognitive disorder known as "chemobrain" which effects up to 16 -50% of individuals receiving long-term adjuvant chemotherapy [ Time Frame: December 2011 ] [ Designated as safety issue: No ]
    To use quantitative FDG-PET, functional MRI (fMRI) and co-registered anatomic MRI imaging to better understand the cognitive disorder known as "chemobrain" which effects up to 16 -50% of individuals receiving long-term adjuvant chemotherapy


Estimated Enrollment: 40
Study Start Date: May 2007
Estimated Study Completion Date: July 2016
Estimated Primary Completion Date: July 2016 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: All patients
All participants enrolled.
Procedure: Imaging assessments
FDG-PET scans, functional MRI (fMRI) scans, Neuropsychological Testing
Other Names:
  • FDG-PET scans
  • functional MRI (fMRI)scans
  • Neuropschological Testing

  Hide Detailed Description

Detailed Description:

In this study, 3 groups of 8 women each, between the ages of 18 and 65, will participate in this study. The "affected patient group" will be women with complaints of memory dysfunction who have received adjuvant chemotherapy (one or more anticancer drugs used in combination with surgery), for the treatment of breast cancer. These patients will be those that are being treated at Huntsman Cancer Institute/Hospital.

The second "patient control group" will be age-matched (same age) women with breast cancer who have undergone similar chemotherapy and have no complaints of memory problems.

The non-patient group will be age-matched (same age) women who have not undergone any type of chemotherapy. These individuals will be recruited from friends of female family members of the two breast cancer groups.

All individuals will be assessed for dementia (intellectual deterioration) and brain problems using the same kind of neuropsychological testing. All subjects will be age-matched as close as possible, to eliminate age related effects. Subjects will be right-handed, primarily-English speakers with normal hearing.

The purpose of this study is to use modern imaging techniques to better understand chemobrain. These imaging techniques include FDG-PET (FDG is the abbreviation for the radiopharmaceutical fluorodeoxyglucose and PET is Positron Emission Tomography) and functional MRI (fMRI)). They will be used to look at the metabolism (chemical activity) in specific areas of the brain and the entire brain overall. By using FDG-PET doctors will see how the brain activates. By using fMRI doctors will see how the brain works when you are challenged with certain mental tasks that make you concentrate and remember. FDG-PET and fMRI might provide important information on the brain that may be connected with chemotherapy.

This study will be an important first step to understand the problem of chemobrain. The imaging evaluations will make it possible to explore the changes in brain function that may be responsible for chemobrain and hopefully make it possible to predict which people may be affected by this problem.

Many people who undergo chemotherapy particularly adjuvant chemotherapy have complained about cognitive dysfunction for many years. This cognitive decline effects up to 16 -50% of individuals receiving long-term adjuvant chemotherapy [Tannock 2004, Matsuda 2005].Cancer survivors frequently refer to this cognitive dysfunction as "chemobrain" or "chemofog." The majority of individuals who are affected are woman who have undergone adjuvant chemotherapy for breast cancer. The table below is a summary of many of the studies that have been performed assessing cognition and chemobrain.

Women who experience chemobrain typically complain of inability to concentrate, memory dysfunction, word finding difficulties, difficulty with learning, slowed processing abilities, and often difficulty with writing and speaking. A particularly disturbing complaint for many individuals is the inability to multitask. Only recently, have researchers begun studying the impact of chemotherapy on cognitive functioning. This is a difficult area to study however. Part of the problem in assessing chemobrain using scientific principals is sorting out which problems are due to chemotherapy and which are due to having a serious illness like cancer that can result in physical debilitation, depression, sleep disruption, hormone shifts, and fatigue--all of which can affect cognitive functioning.

There are a number of theories at to why chemobrain may occur. One is that some types of chemotherapy can cross the blood/brain barrier and cause neurotoxicity. Another is that the cognitive problems are created by certain free radicals, the toxic elements that many types of chemotherapy produce [Joshi 2005]. Another theory is that some people have a genetic background that makes them more susceptible to the effects of chemotherapy. Most likely it is not just a single etiologic factor but a multifactorial process that combine to predispose certain individuals to develop chemobrain. Chemotherapy isn't the only cancer treatment that may cause cognitive disturbance and memory complaints. Other cancer treatments that have been implicated as causing complaints of cognitive dysfunction include hormone therapy, immunotherapy, and radiation therapy. Hormone therapy is common in woman being treated with conventional chemotherapy. It is not entirely clear if women undergoing hormone therapy which alters the amount of systemic estrogen experience memory problems. Some studies link memory to the amount of estrogen in the brain. Other studies haven't found this link.

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion criteria: Pre-screening will be conducted to ensure that all subjects are in good neurologic health with no history of seizures or other neurological disorders, and that they have no ferromagnetic implants or clips in their body. Subjects will be right-handed exclusive-English speakers with normal hearing.

Exclusion criteria: If a subject is found to have profound or severe depression after the Neuropsychological and Cognitive Testing session they may be excluded from the imaging portion of the study. This is justified as the imaging session would not be valid as the biologic correlates of depression rather than chemobrain would be imaged. Subjects found to have profound or severe depression will be notified and appropriate referral made to get them the necessary medical care to treat their depression.

Three cohorts of 8 women each under the age of 65 will be recruited for this exploratory pilot study. The "affected patient cohort" will be woman with complaints of cognitive or memory dysfunction who have received adjuvant chemotherapy for the treatment of breast cancer. These patients will be those being treated at Huntsman Cancer Hospital and be the patients of Dr Saundra Buys or Dr John Ward. The second "patient control cohort" will be age-matched woman with breast cancer who have undergone similar adjuvant chemotherapy for the same amount of time who have no complaints of memory dysfunction. Again these are primarily patients of Drs. Buys or Ward. The non-patient cohort will be age-matched woman who have not undergone any type of chemotherapy. These individuals will be recruited from friends of female family members of the two breast cancer cohorts. All individuals will be assessed for dementia and cognitive impairment using the same battery of dementia and cognitive/neuropsychological testing. All subjects will be age-matched as close as possible to eliminate age related cognitive effects. Subjects will be right-handed exclusive-English speakers with normal hearing. Pre-screening will be conducted to ensure that all subjects are in good neurologic health with no history of seizures or other neurological disorders, and that they have no ferromagnetic implants or clips in their body.

Up to 40 subjects may be enrolled to ensure 24 evaluable subjects.

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00708045

Contacts
Contact: Kelli Rasmussen 801-213-4218 kelli.rasmussen@hci.utah.edu
Contact: Britney Beardmore 801-587-4798 britney.beardmore@hci.utah.edu

Locations
United States, Utah
Huntsman Cancer Institute Recruiting
Salt Lake City, Utah, United States, 84112
Sponsors and Collaborators
University of Utah
Investigators
Principal Investigator: John M Hoffman, MD Huntsman Cancer Institute
  More Information

No publications provided

Responsible Party: University of Utah
ClinicalTrials.gov Identifier: NCT00708045     History of Changes
Other Study ID Numbers: HCI21946
Study First Received: June 27, 2008
Last Updated: July 28, 2014
Health Authority: United States: Institutional Review Board

Keywords provided by University of Utah:
Breast Cancer

ClinicalTrials.gov processed this record on August 19, 2014