Nab-paclitaxel (Abraxane) With or Without Mifepristone in Patients With Advanced Breast Cancer

NCT ID: NCT01493310

Last Updated: 2018-09-12

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 9 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-11-30
• Study Completion Date: 2018-05-31

Brief Summary

This trial will find the best dose of mifepristone when given together with nab-paclitaxel (Abraxane) based on the side effects of the two drugs in patients with advanced breast cancer.

Patients will be randomized to receive nab-paclitaxel with or without mifepristone during the first treatment cycle. After the first cycle, all patients will receive nab-paclitaxel with mifepristone until their disease worsens or they experience an unacceptable side effect.

This study will test up to 4 doses of mifepristone in combination with nab-paclitaxel. The study will first test the lowest dose in a small group of patients and if they do not have bad side effects, higher doses will be tested.

Conditions

Male Breast Cancer; Recurrent Breast Cancer; Stage IIIA Breast Cancer; Stage IIIB Breast Cancer; Stage IIIC Breast Cancer; Stage IV Breast Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Arm A (hormone therapy, chemotherapy)

Patients will receive mifepristone and nab-paclitaxel in 28-day treatment cycles. Patients receive mifepristone once a day by mouth on days 0, 1, 7, 8, 14, and 15 and nab-paclitaxel by intravenous infusion (IV) on days 1, 8, and 15. Treatment cycles are repeated every 28 days in the absence of disease progression or unacceptable side effects.

Group Type: EXPERIMENTAL

mifepristone

Intervention Type: DRUG

Given orally (by mouth)

Up to 4 doses of mifepristone will be studied (300 mg, 600 mg, 900 mg, 1200 mg)

nab-paclitaxel

Intervention Type: DRUG

Given by intravenous infusion (IV)

Dose of 80 mg/m2

Arm B (chemotherapy)

Patients will receive nab-paclitaxel and placebo for a 28-day treatment cycle (Cycle 1).

Patients receive placebo once a day by mouth on days 0, 1, 7, 8, 14, and 15 and nab-paclitaxel by intravenous infusion (IV) on days 1, 8, and 15. Patients then cross-over to Arm A after completion of the first treatment cycle.

Group Type: ACTIVE_COMPARATOR

placebo

Intervention Type: DRUG

Given orally

nab-paclitaxel

Intervention Type: DRUG

Given by intravenous infusion (IV)

Dose of 80 mg/m2

Interventions

mifepristone

Given orally (by mouth)

Up to 4 doses of mifepristone will be studied (300 mg, 600 mg, 900 mg, 1200 mg)

Intervention Type: DRUG

placebo

Given orally

Intervention Type: DRUG

nab-paclitaxel

Given by intravenous infusion (IV)

Dose of 80 mg/m2

Intervention Type: DRUG

Other Intervention Names

Mifegyne; Mifeprex; RU-38486; PLCB; ABI-007; nab paclitaxel; paclitaxel albumin-stabilized nanoparticle formulation; nanoparticle albumin-bound paclitaxel

Eligibility Criteria

Inclusion Criteria

• Patients must have metastatic (stage IV) or unresectable (cannot be removed by surgery) stage III breast cancer
• Patients must have evaluable disease
• Patients may have received adjuvant chemotherapy and up to four prior chemotherapy regimens for metastatic or locally recurrent disease and cannot have received prior nab-paclitaxel or mifepristone therapy for metastatic disease
• Patients who are estrogen receptor (ER)- and/or progesterone receptor (PR)-positive must have developed metastatic disease while on adjuvant hormonal therapy or have progression of disease after at least one hormonal therapy for advanced disease) and may have received unlimited prior hormonal therapies
• Eastern Cooperative Oncology Group (ECOG) performance status 0-2 (Karnofsky > 60%)
• Absolute neutrophil count >= 1,500/mL
• Platelets >= 100,000/mL
• Total bilirubin =< institutional upper limit of normal (ULN)
• AST (serum glutamic oxaloacetic transaminase [SGOT])/ALT (serum glutamic pyruvate transaminase [SGPT]) =< 2.5 X institutional ULN
• Creatinine =< institutional ULN OR creatinine clearance >= 60 mL/min/1.73 m^2 for patients with creatinine levels above institutional normal
• Morning cortisol >= institutional normal
• Negative serum or urine pregnancy test is required for women of child-bearing potential (able to get pregnant)
• Women of child-bearing potential and men who are sexually active must agree to use two forms of birth control prior to study entry and for the duration of study participation
• Ability to understand and the willingness to sign a written informed consent document

Exclusion Criteria

• Patients who have had chemotherapy or radiotherapy within 4 weeks prior to entering the study or those who have not recovered from adverse events due to agents administered more than 4 weeks earlier
• Patients may not be receiving any other investigational drugs or treatments
• Patients with known brain metastases are eligible as long as they have completed radiation to the brain and have been off of corticosteroid therapy for at least 4 weeks
• History of allergic reactions to compounds similar to mifepristone or paclitaxel/nab-paclitaxel; patients with a history of mild infusion reactions with paclitaxel who were able to continue to receive paclitaxel with corticosteroid premedications will be eligible to participate, as these cases were likely related to Cremophor and not paclitaxel
• Mifepristone may affect the way the body processes some types of drugs so they cannot be taken while on-study. These include but are not limited to non-steroidal anti-inflammatory drugs (NSAIDs) or warfarin, cyclosporine, certain benzodiazepines. The study doctor will review patient's current medications to determined if any are prohibited from the study.
• Uncontrolled intercurrent illness or psychiatric illness/social situations that would limit compliance with study requirements
• Pregnant women are excluded from this study; breastfeeding should be discontinued if patient wishes to participate in the study
• Human immunodeficiency virus (HIV)-positive patients on combination antiretroviral therapy are ineligible
• No history of long-term or ongoing short term use of corticosteroids is allowed

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Chicago

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Rita Nanda

Role: PRINCIPAL_INVESTIGATOR

University of Chicago

Locations

University of Chicago

Chicago, Illinois, United States

NorthShore University Health System

Evanston, Illinois, United States

Countries

United States

Other Identifiers

NCI-2011-03525

Identifier Type: REGISTRY

Identifier Source: secondary_id

11-0546

Identifier Type: -

Identifier Source: org_study_id