Breast Cancer Clinical Trial
Oxybutynin Chloride in Managing Hot Flashes
Summary
This randomized phase III trial studies how well oxybutynin chloride works in managing hot flashes in patients who are not candidates for, or not interested in hormone replacement therapy. Previous studies have shown that oxybutynin is effective in managing hot flashes, however doses used in prior studies have resulted in side effects. This trial is evaluating lower doses of oxybutynin with the goal of determining if they are efficacious with less side effects.
ADAM-VTE
Full Description
PRIMARY OBJECTIVES:
I. To determine whether oxybutynin chloride (oxybutynin) can diminish hot-flash activity in women with a history of breast cancer or in women who have a concern about taking estrogen for fear of breast cancer.
SECONDARY OBJECTIVES:
I. To perform a dose-response evaluation of two oxybutynin doses. II. To determine the toxicity of oxybutynin in the study population. III. To assess the impact of hot-flash activity on overall quality of life and to examine whether oxybutynin can diminish this impact on quality of life.
OUTLINE: Patients are randomized into 1 of 4 groups.
GROUP I (LOW-DOSE OXUBUTYNIN CHLORIDE): Patients receive lower dose oxybutynin chloride orally (PO) twice a day (BID) on days 8-49 in the absence of unacceptable toxicity.
GROUP II (LOW-DOSE PLACEBO): Patients receive lower dose placebo PO BID on days 8-49 in the absence of unacceptable toxicity.
GROUP III (HIGH-DOSE OXUBUTYNIN CHLORIDE): Patients receive lower dose oxybutynin chloride PO BID on days 8-14 and higher dose oxybutynin chloride on days 15-49 in the absence of unacceptable toxicity.
GROUP IV (HIGH-DOSE PLACEBO): Patients receive lower dose placebo PO BID on days 8-14 and higher dose placebo on days 15-49 in the absence of unacceptable toxicity.
Eligibility Criteria
Inclusion Criteria:
History of breast cancer, ductal breast carcinoma in situ (DCIS), or lobular carcinoma in situ (LCIS) (currently without evidence of malignant disease) OR a concern about taking estrogen for fear of breast cancer
Bothersome hot flashes (defined by their occurrence of >= 28 times per week and of sufficient severity to prompt the patient to seek therapeutic intervention)
Presence of hot flashes for > 30 days prior to study entry
Ability to complete questionnaire(s) by themselves or with assistance
Eastern Cooperative Oncology Group (ECOG) performance status (PS) = 0, 1
Ability to provide informed written consent
Life expectancy >= 6 months
Willing to work with the enrolling institution for follow-up (during the active monitoring phase of the study)
Exclusion Criteria:
Any of the following current (=< 4 weeks prior) or planned therapies:
Antineoplastic chemotherapy (anti-HER2 agents allowed)
Androgens
Estrogens (any delivery route)
Progestogens
Tamoxifen, raloxifene and aromatase inhibitors are allowed, but patient must have been on a constant dose for at least 28 days and must not be expected to stop the medication during the study period
Selective serotonin reuptake inhibitors (SSRIs)/serotonin?norepinephrine reuptake inhibitors (SNRIs), when being used for hot flash management or other indications such as depression, is allowed, assuming the dose will remain unchanged for the study duration
Gabapentin/pregabalin, when being used for hot flash management (use for other indications, such as pain, is allowed, assuming the dose will remain unchanged for the study duration)
Clonidine
Agents with known potent anticholinergic activity; agents with mild-moderate anticholinergic activity are allowed
Prior use of oxybutynin during the period in which patient has had hot flashes
Pregnant women
Nursing women
History of any of the following contraindications to oxybutynin:
Uncontrolled gastroesophageal reflux disease (GERD) despite appropriate therapy; if patient has history of GERD, but symptoms are well-controlled with medical treatment, patient is eligible
Ulcerative colitis
Narrow-angle glaucoma
Urinary retention
Hypersensitivity to oxybutynin or any other components of the product
Current uncontrolled hyperthyroidism
Coronary heart disease (angina or prior myocardial infarction)
Congestive heart failure
Symptomatic cardiac arrhythmias
Current uncontrolled hypertension
Myasthenia gravis
Dementia
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There are 13 Locations for this study
Peoria Illinois, 61615, United States
Urbana Illinois, 61801, United States
Cedar Rapids Iowa, 52403, United States
Wichita Kansas, 67214, United States
Edgewood Kentucky, 41017, United States
Ann Arbor Michigan, 48106, United States
Rochester Minnesota, 55905, United States
Cary North Carolina, 27518, United States
Anderson South Carolina, 29621, United States
Rapid City South Dakota, 57701, United States
Green Bay Wisconsin, 54301, United States
Madison Wisconsin, 53792, United States
Marshfield Wisconsin, 54449, United States
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