Visualization of the Effect of Acupuncture on Brain Serotonin in Breast Cancer Survivors



Status:Completed
Conditions:Breast Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:March 2009
End Date:December 2010

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Effect of Acupuncture on Brain Serotonin Among Breast Cancer Survivors

RATIONALE: New imaging procedures, such as single photon emission computed tomography, may
help in learning how acupuncture affects serotonin levels in the brain of breast cancer
survivors. PURPOSE: This phase I trial is studying the best way to visualize the effect of
acupuncture on brain serotonin in breast cancer survivors.

Detailed Description

OBJECTIVES:

I. To determine the feasibility of using [123-I] ADAM Serotonin transporter (SERT) binding
as a putative biomarker to visualize the mechanism of effects of acupuncture for hot flashes
involving serotonin.

OUTLINE: Patients undergo acupuncture twice weekly for 2 weeks and then once weekly for 6
weeks. Patients undergo single photon emission computed tomography imaging with iodine 123-I
ADAM before and after completion of acupuncture.

After completion of study treatment, patients are followed for 4 weeks.

Inclusion Criteria:

- History of Stage I, II, or III breast cancer for at least 12 months

- Have been seen by an oncologist within the previous 6-month period and determined to
be free of disease by clinical examination and history

- Have been receiving endocrine therapy (tamoxifen or aromatase inhibitors for at least
four weeks)

- Experienced hot flashes with a hot flash composite score of 5 or greater per day

- Hot flashes have been present for at least a month before study entry

Exclusion Criteria:

- Currently on chemotherapy or radiation therapy as adjuvant treatment

- Started with hormonal therapies such as tamoxifen or aromatase inhibitors within the
last 4 weeks; or plan to change or terminate hormonal therapies in the next 14 weeks

- Any history of use of psychotropic medication such as SSRI use for the past 6 months

- Any past use of centrally acting medications such as clonidine for the past 6 months

- Any past diagnosis of a Major Depressive Episode within the last 6 months

- Any allergy to iodine or shell-fish or radio-nuclear materials

- Current use of estrogen and/or progestin

- Pregnancy

- Breast feeding

- Women of child-bearing potential NOT willing to use a medically acceptable form of
contraception

- Current use of any anti-convulsant such as gabapentin

- History of cerebral infarction (including lacunar infarct with symptoms >= 24 hours
duration)

- History of Binswanger's disease (or a history of hypertensive encephalopathy)

- History of intracranial hemorrhage

- History of head trauma with loss of consciousness

- History of encephalitis

- History of extended exposure to known neurotoxin (e.g., cyanide, carbon monoxide)

- Uncontrolled metabolic disorder (e.g., thyroid disease, diabetes mellitus)

- History of normal pressure hydrocephalus

- History of Parkinson's or other basal ganglia disease

- History of substance abuse in the previous 6 months
We found this trial at
1
site
3400 Civic Center Blvd
Philadelphia, Pennsylvania 19104
(215) 662-6065
Abramson Cancer Center of the University of Pennsylvania The Abramson Cancer Center of the University...
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mi
from
Philadelphia, PA
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