Recruiting
STUDY02001740;22SCH740: Estradiol For ER+ Advanced Breast Cancer (ESTHER)
Determine whether subjects harboring ESR1-mutant/amplified breast cancer have a higher rate of clinical benefit from 17b-estradiol therapy than subjects with ESR1-wild-type breast cancer
ClinicalTrials.gov IDNCT05716516
PhasePHASE2
Enrollment36
SponsorDartmouth-Hitchcock Medical Center
Age18 Years
SexFEMALE
Conditions studied
Metastatic Breast Cancer
About this study
Determine whether subjects harboring ESR1-mutant/amplified breast cancer have a higher rate of clinical benefit from 17b-estradiol therapy than subjects with ESR1-wild-type breast cancer
Interventions
- Drug: Estradiol — Estradiol is a therapeutic option for the treatment of advanced ER+ breast cancer
Primary outcomes
- Clinical Benefit Rate (12 months)
Eligibility information
Inclusion Criteria:
* Post-menopausal women with ER+ breast cancer.
* Metastatic or locoregional recurrence not amenable to treatment with curative
* intent.
* Received ≥1 prior line of endocrine-based therapy (e.g., including tamoxifen, aromatase inhibitors, fulvestrant, or combinations) in the advanced/metastatic setting
Exclusion Criteria:
* During the study Treatment Phase with 17b-estradiol, no concurrent anti-cancer therapies are allowed with the following exceptions:
* Exception: Trastuzumab is allowed for the treatment of subjects with a history of HER2+ disease, and will be used at the physician's discretion.
* Exception: Anti-resorptive bone therapies (e.g., bisphosphonates, denosumab) are permitted.
* Any investigational cancer therapy in the last 3 weeks.
* Known CNS disease, unless clinically stable for ≥ 3 months.
* History of any of the following:
* Deep venous thrombosis.
* Pulmonary embolism.
* Stroke.
* Acute myocardial infarction.
* Congestive heart failure.
* Previous malignancy not treated with curative intent, or with an estimated recurrence risk ≥30%.
Study locations
- Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire 03756 United States
Before you participate: Varda Clinical is an independent discovery tool, not the study sponsor or a medical provider. Eligibility can only be determined by the official study team. Discuss potential risks and benefits with a qualified healthcare professional.
Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-09-27.