About this trial
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.
Eligibility criteria
Qualifiers
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
Disqualifiers
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
Trial design
Treatments tested in this trial
- Minoxidil
- Minoxidil
- Quality-of-Life Assessment
- Questionnaire Administration
Treatment groups
Locations
1Sponsors and collaborators
Ohio State University Comprehensive Cancer Center
Lead sponsor