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Spots Global Cancer Trial Database for Orteronel as Monotherapy in Patients With Metastatic Breast Cancer (MBC) That Expresses the Androgen Receptor (AR)

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Trial Identification

Brief Title: Orteronel as Monotherapy in Patients With Metastatic Breast Cancer (MBC) That Expresses the Androgen Receptor (AR)

Official Title: A Phase II Study With Orteronel as Monotherapy in Patients With Metastatic Breast Cancer (MBC) That Expresses the Androgen Receptor (AR)

Study ID: NCT01990209

Interventions

Orteronel

Study Description

Brief Summary: The androgen receptor (AR) is expressed in 70-90 percent of primary breast tumors and in 75 percent of breast metastases. There is evidence to suggest that Androgen Receptor (AR) may be a target in patients with advanced breast cancer. Breast cancer patients whose tumors do not express the ER, PR or HER2 (triple negative) have very few options for treatment. Orteronel is being developed as an endocrine therapy for relevant hormone-sensitive cancers such as prostrate cancer and breast cancer. Triple-negative metastatic breast cancer patients with AR expression could potentially benefit from anti-androgen therapy like orteronel.

Detailed Description: This open-label multicenter study will be conducted in 2 stages. * Lead-in Phase: The first 6 patients treated will be evaluated to confirm the safety and feasibility of this regimen. After all 6 patients complete at least 4 weeks of treatment, and if no prohibitive toxicities are identified, continuous study treatment will begin. * Continuous Study Treatment: Patients will continue to be enrolled into both cohorts based on their tumor specificities with an anticipated total of 31 patients in Cohort 1 (ER-/PR-/HER2-/AR+) and an anticipated total of 55 patients in Cohort 2 (ER+ and/or PR+/AR+). Patients will be evaluated every eight weeks for response to treatment. All patients who respond to treatment (complete response \[CR\] or partial response \[PR\]) or have stable disease (SD) will continue to receive orteronel until they develop progressive disease (PD) or unacceptable toxicity.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Yale School of Medicine, New Haven, Connecticut, United States

Northeast Georgia Medical Center, Gainesville, Georgia, United States

Hope Cancer Center, Terre Haute, Indiana, United States

Baptist Hospital East, Louisville, Kentucky, United States

Center for Cancer and Blood Disorders, Bethesda, Maryland, United States

Cancer Research Consortium of West Michigan, Grand Rapids, Michigan, United States

Cancer Centers of SW Oklahoma, Lawton, Oklahoma, United States

Tennessee Oncology PLLC, Chattanooga, Tennessee, United States

Tennessee Oncology PLLC, Nashville, Tennessee, United States

Center for Cancer and Blood Disorders, Fort Worth, Texas, United States

Contact Details

Name: Howard A Burris, III, MD

Affiliation: SCRI Development Innovations, LLC

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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