Overview

Re-expression of ER in Triple Negative Breast Cancers

Status:
Terminated
Trial end date:
2014-01-01
Target enrollment:
0
Participant gender:
All
Summary
Patients are being asked to take part in this study because they have metastatic breast cancer that is triple negative (does not express estrogen receptor (ER), progesterone receptor (PR) or HER2). This means that agents such as trastuzumab (Herceptin®) and tamoxifen are not currently treatment options for their cancer. Another option for treating the patient's cancer at this point is with chemotherapy. The patient should discuss this and other options with their doctor prior to entering this study. Laboratory studies have demonstrated that ER is actually present in some triple negative breast cancers but is "silenced" (does not function properly) because methyl and histone groups are attached to it and inactivate it. Special drugs called demethylating inhibitors (such as decitabine) and histone deacetylase inhibitors (such as LBH589) can remove these methyl and histone groups and reactivate ER. This reactivated ER can then be targeted with agents like tamoxifen. The patient is being asked to join this clinical research study to find out if ER can be reactivated in their cancer using decitabine in combination with LBH589. If ER is reactivated in their cancer, we will then determine if tamoxifen can decrease the growth of the cancer.
Phase:
Phase 1/Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Emory University
Collaborators:
Eisai Inc.
Novartis
Treatments:
Azacitidine
Decitabine
Panobinostat
Tamoxifen
Criteria
Inclusion Criteria:

- Histologically or cytologically confirmed triple negative (ER-, PR-, HER2-) metastatic
or locally advanced breast cancer

- Measurable disease according to the Response Evaluation Criteria in Solid Tumors
(RECIST) criteria.

- Disease that is assessable to biopsy for hormone receptor measurement

- At least one line of therapy prior to study entry (acceptable therapies include
chemotherapy ± anti-angiogenic therapy). Other investigational therapies except DNA
methyltransferase (DNMT) and histone deacetylase (HDAC) inhibitors are allowed.

- Age > 18 years

- Eastern Cooperative Oncology Group (ECOG) Performance Score of 0 or 1 (Appendix A)

- Adequate bone marrow as evidenced by:

- Absolute neutrophil count > 1,500/μL

- Platelet count > 100,000/μL

- Adequate renal function as evidenced by serum creatinine < 1.5 mg/dL

- Adequate hepatic function as evidenced by:

- Serum total bilirubin < 1.5 mg/dL

- Alkaline phosphatase < 3 times the upper limit of normal (ULN) for the reference
lab (< 5 times the ULN for patients with known hepatic metastases

- Serum glutamic-oxaloacetic transaminase (SGOT)/serum glutamic-pyruvic
transaminase (SGPT) < 3 times the ULN for the reference lab (< 5 times the ULN
for patients with known hepatic metastases

- Patients must be recovered from both the acute and late effects of any prior surgery,
radiotherapy or other antineoplastic therapy

- Patients or their legal representatives must be able to read, understand and provide
informed consent to participate in the trial.

- Consent to biopsy before and after therapy with decitabine and LBH589.

- Patients of childbearing potential and their partners must agree to use an effective
form of contraception during the study and for 90 days following the last dose of
study medication (an effective form of contraception is an oral contraceptive or a
double barrier method)

Exclusion Criteria:

- Patients with an active infection or with a fever > 101.30 F within 3 days of the
first scheduled day of protocol treatment

- Patients with active central nervous system (CNS) metastases. Patients with stable CNS
disease, who have undergone radiotherapy at least 4 weeks prior to the planned first
protocol treatment and who have been on a stable dose of corticosteroids for >3 weeks
are eligible for the trial

- History of prior malignancy within the past 5 years except for curatively treated
basal cell carcinoma of the skin, cervical intra-epithelial neoplasia, or localized
prostate cancer with a current prostate-specific antigen (PSA) of < 1.0 mg/dL on 2
successive evaluations, at least 3 months apart, with the most recent evaluation no
more than 4 weeks prior to entry

- Patients with known hypersensitivity to any of the components of decitabine or LBH589

- Patients who received radiotherapy to more than 25% of their bone marrow; or patients
who received any radiotherapy within 4 weeks of entry

- Patients who are receiving concurrent investigational therapy or who have received
investigational therapy within 28 days of the first scheduled day of protocol
treatment (investigational therapy is defined as treatment for which there is
currently no regulatory authority approved indication)

- Peripheral neuropathy >= Grade 2

- Patients who are pregnant or lactating

- Any other medical condition, including mental illness or substance abuse, deemed by
the Investigator to be likely to interfere with a patient's ability to sign informed
consent, cooperate and participate in the study, or interfere with the interpretation
of the results.

- History of allogeneic transplant

- Known HIV or Hepatitis B or C (active, previously treated or both)