Chemotherapy-induced Cognitive and Brain Changes in Older Adults With Breast Cancer

Description

This research study evaluates the effect of chemotherapy on cognition (thinking) and the brain in people with breast cancer.

Conditions

Impaired Cognition, Chemo-brain, Breast Cancer

Study Overview

Study Details

Study overview

This research study evaluates the effect of chemotherapy on cognition (thinking) and the brain in people with breast cancer.

Chemotherapy-induced Cognitive and Brain Changes in Older Adults With Breast Cancer

Chemotherapy-induced Cognitive and Brain Changes in Older Adults With Breast Cancer

Condition
Impaired Cognition
Intervention / Treatment

-

Contacts and Locations

Boston

Massachusetts General Hospital, Boston, Massachusetts, United States, 02114

Salem

Massachusetts General Hospital/North Shore Cancer Center, Salem, Massachusetts, United States, 01970

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Breast cancer patients treated with chemotherapy- Group 1 (experimental group)
  • * Participants must meet the following criteria on screening examination to be eligible to participate in the behavioral +/- imaging components of study
  • * New diagnosis histologically confirmed invasive breast cancer
  • * Treatment plan to include chemotherapy
  • * Female subjects age ≥ 60 years.
  • * Life expectancy ≥ 1 year
  • * Karnofsky Performance Score (KPS) ≥ 80
  • * Ability to understand and the willingness to sign a written informed consent document.
  • * Non-treated breast cancer patient controls- Group 2 (control group)
  • * Participants must meet the following criteria on screening examination to be eligible to participate in the behavioral +/- imaging components of study:
  • * New diagnosis histologically confirmed invasive breast cancer
  • * Treatment plan does not include chemotherapy
  • * Age ≥ 60 years.
  • * Life expectancy ≥ 1 year
  • * Karnofsky Performance Score (KPS) ≥ 80
  • * Ability to understand and the willingness to sign a written informed consent document.
  • * Healthy control subjects- Group 3 (control group)
  • * Participants must meet the following criteria on screening examination to be eligible to participate in the behavioral +/- imaging components of study:
  • * Age ≥ 60 years.
  • * Life expectancy ≥ 1 year
  • * Karnofsky Performance Score (KPS) ≥ 80
  • * Ability to understand and the willingness to sign a written informed consent document.
  • * Participants with well-controlled vascular risk factors, such as treated hypertension, treated hyperlipidemia or well-controlled Type II diabetes (glucose levels \<250) may be included.
  • * Serum Pregnancy Testing: STAT quantitative serum hCG pregnancy testing for all women of childbearing potential. Imaging will not start until and unless the test result returns negative.
  • * Participants who exhibit any of the following conditions at screening will not be eligible for admission into the study:
  • * Participants with clinical or radiographic evidence of metastatic CNS disease
  • * Subjects with MMSE scores below 24
  • * Active or history of major psychiatric disorders such as schizophrenia, schizoaffective disorder, major affective disorder in mid-life, or treatment with ECT (Mild depression that is well treated with stable dose of SSRI antidepressants may be allowed).
  • * Substance abuse within the past 2 years
  • * Huntington's disease, hydrocephalus or seizure disorder
  • * In addition to exclusion criteria above, participants who exhibit any of the following conditions at screening will not be eligible for admission into imaging portion of the study:
  • * Participants with contraindications to MRI (i.e., implanted metal including pacemakers, cerebral spinal fluid shunts, aneurysm clips, artificial heart valves, ear implants or metal/foreign objects in the eyes and those with a history of claustrophobia), injuries to the eyes with metal without X-ray documentation that metal was removed

Ages Eligible for Study

60 Years to

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Massachusetts General Hospital,

Michael Parsons, PhD, PRINCIPAL_INVESTIGATOR, Massachusetts General Hospital

Study Record Dates

2027-01