Study of Donepezil in Female Breast Cancer Survivors With Cognitive Dysfunction

NCT ID: NCT01466270

Last Updated: 2021-10-20

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 62 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-07-31
• Study Completion Date: 2013-10-01

Brief Summary

RATIONALE: Donepezil hydrochloride may help lessen cognitive dysfunction caused by chemotherapy.

PURPOSE: This phase II trial is studying donepezil hydrochloride in treating cognitive dysfunction after chemotherapy in female breast cancer survivors.

Detailed Description

OBJECTIVES:

Primary

• Determine the feasibility of conducting a randomized placebo-controlled clinical trial for cognitive symptoms in female breast cancer survivors.

Secondary

• Estimate the variability of the clinical outcomes (FACT-Cognition Perceived Cognitive Impairment subscale, neurocognitive battery, FACIT-Fatigue, FACT Cog Total Score, PROMIS Fatigue, Epworth Sleepiness Scale, Beck Depression Inventory, Beck Anxiety Inventory, and RAND Short Form-36).
• Estimate the within patient correlation over time of the clinical outcomes.
• Obtain preliminary estimates of the effect of donepezil on the primary and secondary outcome variables.
• Correlate the reports of fatigue, sleep disturbance, and mood with measures of cognitive symptoms and neurocognitive test performance.
• Document the severity of cognitive symptoms and functional impairment in female breast cancer survivors who enroll on this pilot study.
• Correlate cognitive symptoms with cognitive test performance.
• Document the toxicities associated with donepezil hydrochloride use.

OUTLINE: This is a randomized, double-blind, placebo-controlled, multicenter study. Patients are stratified according to menopausal status (pre- vs peri-/post-menopausal) and time since end of chemotherapy (12-36 months vs 36.01-60 months).

Arm I: Patients receive donepezil hydrochloride orally (PO) once daily (QD).

Arm II: Patients receive placebo PO QD.

In both arms treatment continues for 24 weeks.

Patients complete the entire battery of neurocognitive tests and questionnaires (FACT-Cognition Perceived Cognitive Impairment subscale, neurocognitive battery, FACIT-Fatigue, FACT Cog Total Score, PROMIS Fatigue, Epworth Sleepiness Scale, Beck Depression Inventory, Beck Anxiety Inventory, and RAND Short Form-36) at baseline (pre-treatment), 24 weeks (end of medication), and 36 weeks (end of wash-out).

After completion of therapy, patients are followed at 12 weeks.

Conditions

Anxiety Disorder; Breast Cancer; Cognition Disorders; Depression; Fatigue; Sleep Disorders

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Arm I

Patients receive donepezil hydrochloride PO QD.

Group Type: EXPERIMENTAL

donepezil hydrochloride

Intervention Type: DRUG

Given PO

Arm II

Patients receive placebo PO QD.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Given PO

Interventions

donepezil hydrochloride

Given PO

Intervention Type: DRUG

Placebo

Given PO

Intervention Type: DRUG

Other Intervention Names

Donepezil

Eligibility Criteria

Inclusion Criteria

• Adults >18 years old.
• Female with history of invasive breast cancer
• Must have completed adjuvant chemotherapy between 1 and 5 years prior to registration
• Received at least 4 cycles of cytotoxic chemotherapy
• Documentation of prior chemotherapy
• Patients receiving ongoing hormonal therapy for breast cancer must be on the same hormonal agent for at least 3 months prior to study registration and continue for the duration of the study (9 months)
• Karnofsky Performance Status must be > 60 or ECOG 0-2.
• Use of psychotropic medications (anti-depressants, anxiolytics, sleeping aids, narcotics) is permitted. Patient will be asked to list any that have been taken within the last 3 days on the recent medication sheet.
• Patients must be able to give informed consent to participate in the study, including signing the consent form.
• Self-reported cognitive disruption (FACT-Cog Version 3 Perceived Cognitive Impairments sub-score of < 63)
• Negative serum pregnancy test within 10 days prior to registration for women of child-bearing potential.

Exclusion Criteria

• Evidence or suspected recurrent or metastatic disease
• History of dementia, Alzheimer's disease, multi-infarct dementia or CVA (history of transient ischemic attack (TIA is allowed)
• Current use of donepezil, galantamine, rivastigmine, tacrine, memantine, methylphenidate, dextroamphetamine, or any other specific cognition enhancing drugs.are not allowed. For patients who have used these medications they must not have used them within 4 weeks prior to registration.

Patients may not currently be taking Ketoconazole or Quinidine

• Hypersensitivity to donepezil.
• Use of investigational medications within the last 30 days.
• Prior brain metastasis
• Traumatic brain injury, multiple sclerosis or recent myocardial infarction
• History of schizophrenia, psychosis or substance abuse
• Untreated current severe depression. (Currently treated depression is permitted if treatment is stable.)
• Acute severe fatigue, chronic fatigue syndrome or fibromyalgia.
• History of hepatic or renal dysfunction or disease
• Pregnant women are excluded from this study. The effects of donepezil on the developing human fetus at the recommended therapeutic dose are unknown. For this reason and because donepezil is known to be teratogenic, women of child-bearing potential 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 study physician immediately.
• It is unknown whether donepezil is excreted in breast milk, for this reason women who are currently breast-feeding are not eligible for this study.

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: collaborator

Wake Forest University Health Sciences

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Julia A. Lawrence

Role: PRINCIPAL_INVESTIGATOR

Wake Forest University Health Sciences

Other Identifiers

U10CA081851

Identifier Type: NIH

Identifier Source: secondary_id

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REBACCCWFU 97211

Identifier Type: OTHER

Identifier Source: secondary_id

IRB00019792-1

Identifier Type: -

Identifier Source: org_study_id