Mifepristone and Eribulin in Patients With Metastatic Triple Negative Breast Cancer or Other Specified Solid Tumors

Corcept Therapeutics

Status and phase

Completed

Phase 1

Conditions

Breast Cancer

Sarcoma

Ovarian Epithelial Cancer Recurrent

Non-small Cell Lung Cancer

Prostatic Neoplasms

Carcinoma, Transitional Cell

Prostate Cancer

Treatments

Drug: Mifepristone and Eribulin in combination

Study type

Interventional

Funder types

Industry

Identifiers

NCT02014337

C1073-500

Details and patient eligibility

About

This is a study to assess the safety of the combination of mifepristone and eribulin in patients with metastatic or locally advanced unresectable breast or other specified solid tumors, and determine preliminary efficacy of the combination of mifepristone and eribulin in patients with metastatic or locally advanced unresectable Triple Negative Breast Cancer (TNBC). The structure for the study is a single arm, non-randomized, open-label, multicenter trial with no control group. The study will be conducted at up to 11 sites, with up to 40 evaluable patients

Full description

There will be two parts to the study: Part 1, a dose escalation phase, in which the MTD and RP2D will be determined in up to 20 patients with metastatic breast or other specified solid tumors, regardless of receptor status; and Part 2, a dose expansion phase in which a preliminary estimate of efficacy will be made in an expansion group of up to 20 patients with glucocorticoid receptor-positive metastatic TNBC at the RP2D.

Treatment will be administered in 21-day cycles, with the exception of the first cycle, which will be of 28 days duration with a lead-in of 7 days dosing of mifepristone.

Cycle 1 (28-day cycle): Mifepristone administered orally (PO) with food once daily for 28 days. Eribulin will be administered intravenously (IV) over 2 to 5 minutes on days 8 and 15.

Cycle 2 and beyond (21-day cycle): Mifepristone administered orally (PO) with food once daily for 21 days. Eribulin will be administered intravenously (IV) over 2 to 5 minutes on days 1 and 8.

Enrollment in Part 2 of the study (dose expansion) will occur once the RP2D has been determined. Patients in the dose expansion study must have TNBC disease that is glucocorticoid receptor-positive (by immunohistochemistry [IHC]). Patients will be treated in repeated 21-day cycles until progression or another withdrawal criterion is met.

Part 1 of the study is complete. Part 2 of the study is ongoing.

Enrollment

37 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Informed consent given prior to study-specific screening procedures
≥ 18 years old

Part 2, dose expansion:

Diagnosis of TNBC: < 1% cells positive for ER/progesterone receptor, and HER2 IHC score of 0 or 1, or FISH HER2+ ratio of less than 1.8; patients with low ER IHC (> 1% but < 10% cells positive), but negative by genomic assay are eligible
Inoperable metastatic or locally advanced unresectable disease
Patients should have received a minimum of one, and up to five prior chemotherapy regimens
Must have submitted a diagnostic FFPE tumor tissue sample to confirm tumor GR positivity. Tumor tissue may be from primary or metastatic lesion. In the absence of sufficient tissue to complete IHC, a tumor biopsy will be required.
Tumor must be glucocorticoid receptor positive TNBC (≥10% positive cells by IHC of tumor biopsy)
Must have measurable disease (RECIST v1.1) in at least one lesion not previously irradiated unless documented evidence of progression
Patients with treated, stable brain metastases eligible providing treatment was ≥4 weeks prior to initiation of study drug, and baseline CT or MRI negative for new brain metastases. Must not require therapy with corticosteroids.
ECOG performance status 0 or 1
Must have adequate bone marrow and renal/hepatic function at the screening visit (≤7 days preceding the lab assessment):

i. ANC ≥ 1,500/mm3, without G-CSF

ii. Platelets ≥ 100,000/mm3, without transfusion

iii. Hemoglobin ≥ 9 g/dL, without transfusion support

iv. AST or ALT ≤ 3 × ULN

v. Total serum bilirubin ≤ 1.5 times ULN

vi. Serum creatinine ≤ ULN

vii. Potassium and magnesium levels within normal limits. If below the lower limit of normal, must have levels corrected by supplementation prior to starting study drug.

viii. albumin > 3.0 g/dL
PT/aPIT ≤ 1.5 x ULN
Disease-free period of > 3 years from any other previous malignancies, excluding curatively treated basal cell carcinoma, squamous cell carcinoma of the skin, or carcinoma in situ of the cervix.
Female patients of childbearing potential must have a negative serum pregnancy test. Sexually active patients must be willing to use non-hormonal contraception, including condom use by male partner, and barrier method by the female partner during the treatment period and for at least 3 months after the last dose of the study drug. Females considered not of childbearing potential include those who have been in menopause > 2 years, or are surgically sterile (status post tubal ligation or hysterectomy).
Must be able and willing to comply with the study visit schedule and study procedures.
Able to take oral medications

Exclusion criteria

Systemic cytotoxic therapies or radiotherapy ≤14 days prior to day 1 cycle 1
Major surgery within 4 weeks, or minor surgery within 2 weeks prior to day 1 of cycle 1
Endometrial bleeding
For two weeks prior to day 1 cycle 1, administration of specified cytochrome P450 3A (CYP3A) inducers
Patients who are taking simvastatin or lovastatin. Patients should be switched to alternative therapies a minimum of 2 weeks before starting study drug
Patients who have been treated with an investigational agent <21 days prior to day 1 of cycle 1
Concomitant use of biological agents including growth factors. Exception: 3- to 6-patient breast cancer cohort enrolled to explore the use of prophylactic growth-factor support of a 1.4 mg/m2 dose of eribulin.
Patients who require treatment with systemic corticosteroids for serious medical conditions or illnesses (e.g. immunosuppression after organ transplantation)
History of significant cardiac disease. Includes second/third degree heart block; significant ischemic heart disease; mean QTc interval > 480 msec prior to study start; poorly controlled hypertension; congestive heart failure of NYHA Class II or worse
Pregnant or breast-feeding
Any other significant co-morbid conditions that would impair study participation or cooperation
In Part 2, unable or unwilling to consent to provision of tumor tissue for GR assay