Anatomic Stage III Breast Cancer AJCC v8 Clinical Trial
Official title:
A Pilot Trial of Topical vs Oral Minoxidil for Treatment of Endocrine Therapy-Induced Alopecia in Breast Cancer Patients
This early phase I trial studies the possible benefits and/or side effects of topical or oral minoxidil in treating endocrine therapy-induced hair loss (alopecia) in patients with stage I-IV breast cancer. Endocrine therapy-induced alopecia (EIA) is a distressing side effect that leads to reduced quality of life and early cessation of therapy in women undergoing treatment for breast cancer. Patients on endocrine therapy commonly report hair loss or thinning. Minoxidil is a drug that may promote hair growth and reduce hair loss. Oral minoxidil may increase hair density in women with EIA, and work the same as topical minoxidil in treating EIA in patients with breast cancer.
Status | Recruiting |
Enrollment | 50 |
Est. completion date | December 31, 2024 |
Est. primary completion date | December 31, 2024 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Women >= 18 years of age - Established diagnosis of breast cancer stages I-IV - On endocrine therapy including tamoxifen or aromatase inhibitors with or without concurrent use of ovarian function suppression - Self-reporting hair loss since starting endocrine therapy Exclusion Criteria: - Pregnant or nursing women - Current chemotherapy use or prior chemotherapy use within the last 2 years - History of scarring/cicatricial alopecia or alopecia areata - Prior use of oral or topical minoxidil - Prior or ongoing use of spironolactone - Known sensitivity to minoxidil - Untreated hypothyroidism or iron deficiency as determined by thyroid stimulating hormone (TSH) with reflex free T4 and ferritin level > 40 to be checked at the time of enrolling if not completed in the 12 months prior |
Country | Name | City | State |
---|---|---|---|
United States | Ohio State University Comprehensive Cancer Center | Columbus | Ohio |
Lead Sponsor | Collaborator |
---|---|
Ohio State University Comprehensive Cancer Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Proportion of days assigned medication was taken/applied | For the oral minoxidil group, the proportion of pills taken will be reported with a 95% confidence interval. For the topical minoxidil group, the proportions of days medication was applied will be reported with a 95% confidence interval. | Up to 12 months | |
Secondary | Occurrence of at least one adverse event (AE) of grade 1 or higher | Adverse events will be summarized using National Cancer Institute Common Terminology Criteria for Adverse Events version 5.0 with reporting of the number and percentage of patients affected. The total number of participants with AEs of any grade, and the total number of participants with grade 3 or higher AEs will be compared between randomized groups using Fisher's exact test. | Up to 12 months | |
Secondary | Change in hair density | At least mild-to-moderate improvement in hair density from baseline to 3 months as determined by a board-certified dermatologist from photographs. Will construct two-sided 95% confidence intervals for improvements from baseline and differences between randomized groups. Response will be dichotomized as no improvement versus moderate-to-significant improvement. | Baseline to 3 months | |
Secondary | Change in hair density | At least mild-to-moderate improvement in hair density from baseline to 6 months as determined by a board-certified dermatologist from photographs. Will construct two-sided 95% confidence intervals for improvements from baseline and differences between randomized groups. Response will be dichotomized as no improvement versus moderate-to-significant improvement. | Baseline to 6 months | |
Secondary | Change in hair density | At least mild-to-moderate improvement in hair density from baseline to 12 months as determined by a board-certified dermatologist from photographs. Will construct two-sided 95% confidence intervals for improvements from baseline and differences between randomized groups. Response will be dichotomized as no improvement versus moderate-to-significant improvement. | Baseline to 12 months | |
Secondary | Chemotherapy Alopecia Distress Scale (CADS) score | Patients will complete a a self-administered 17-item questionnaire | At 3 months | |
Secondary | CADS score physical | a self-administered 17-item questionnaire which categorizes questions into 4 subscales including physical | At 6 months | |
Secondary | CADS score physical | a self-administered 17-item questionnaire which categorizes questions into 4 subscales including physical relationship | At 6 months | |
Secondary | CADS score emotional | a self-administered 17-item questionnaire which categorizes questions into 4 subscales including emotional relationship | At 12 months | |
Secondary | Patient-reported outcomes | Mean responses to the symptom experience diary questions and the satisfaction items will be compared between groups via t-test. | At 3 months | |
Secondary | Patient-reported outcomes | Mean responses to the symptom experience diary questions and the satisfaction items will be compared between groups via t-test. | At 6 months | |
Secondary | Patient-reported outcomes | Mean responses to the symptom experience diary questions and the satisfaction items will be compared between groups via t-test. | At 12 months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Suspended |
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