Evaluation of the Use of AZD6244 to Induce Increased ER Expression and Anti-Estrogen Response in ER-Negative/Low Breast Cancer

University of Miami

Status and phase

Completed

Early Phase 1

Conditions

Breast Cancer

Treatments

Drug: AZ6244

Study type

Interventional

Funder types

Other

Identifiers

NCT01313039

20100252

Details and patient eligibility

About

If AZD6244 is able to increase ER expression in ER-negative/low cancers then it may be possible to effectively use hormonal therapy in these patients resulting in improved outcomes. The investigators propose a single-arm Simon two-step study to examine whether treatment with AZD6244 will result in increased ER expression in ER-negative/low primary breast tumors.

Enrollment

4 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Female breast cancer patient > 18 years.
Patients must have biopsy-proven clinical Stage Ic-III invasive breast carcinoma with ≤ 10% ER expression by immunohistochemistry (IHC) analysis.
Patients must have a pre-treatment baseline core biopsy or incisional biopsy available for additional testing (ER, protein/gene expression analysis).
Patients must have sufficient tumor remaining following diagnostic biopsy that requires an additional definitive surgical procedure per the standard of care. Planned procedure may include lumpectomy or mastectomy as clinically indicated.
Patients must have an ECOG Performance Status of 0 - 1.
Patients must have the ability to understand and willingness to sign an English or a Spanish language written informed consent document.

Exclusion criteria

Male breast cancer patient.
Patients who are pregnant or breast-feeding are excluded from the study due to potential harm to the fetus or nursing infant from the study therapy. Patients of reproductive potential must consent to use of contraception or abstinence to be eligible for the study.
Patients may not have received prior chemotherapy or hormonal therapy for treatment of the current breast cancer.
Patients should not have known or strongly suspected BRCA mutation by history (genetic testing not required).
Patients will have pre-study testing, including history and physical exam, complete blood count, and measurement of renal and hepatic function. Patients will be ineligible for the study if significant abnormalities are detected, in accordance with good medical practice.