Testing the Addition of an Anti-cancer Drug, ASTX727 (Cedazuridine, Decitabine), to Chemotherapy (Paclitaxel) and Immunotherapy (Pembrolizumab) for Metastatic Triple-Negative Breast Cancer
Part of paid clinical trials in Phoenix, Arizona.
- Sponsor
- National Cancer Institute (NCI)
- Study ID
- NCT05673200
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Anatomic Stage III Breast Cancer AJCC v8
- Anatomic Stage IV Breast Cancer AJCC v8
- Metastatic Triple-Negative Breast Carcinoma
- Unresectable Triple-Negative Breast Carcinoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Biopsy Procedure — PROCEDUREUndergo biopsy
- Biospecimen Collection — PROCEDUREUndergo collection of blood
- Computed Tomography — PROCEDUREUndergo CT
- Decitabine and Cedazuridine — DRUGGiven PO
- Magnetic Resonance Imaging — PROCEDUREUndergo MRI
- Paclitaxel — DRUGGiven IV
- Pembrolizumab — BIOLOGICALGiven IV
Study Details
This phase I trial tests the safety, side effects, and best dose of ASTX727 when given in combination with a usual approach of treatment with paclitaxel and pembrolizumab in patients with triple-negative breast cancer that has spread from where it first started (primary site) to other places in the body (metastatic). The usual approach is defined as care most people get for this type of cancer. The usual approach for patients with metastatic triple negative breast cancer who are not in a study is chemotherapy with drugs like paclitaxel, carboplatin, cisplatin, eribulin, vinorelbine, capecitabine, gemcitabine, doxorubicin or cyclophosphamide. There is a protein called PD-L1 that helps regulate the body's immune system. For patients who have PD-L1+ tumors, immunotherapy (pembrolizumab) is usually added to paclitaxel or carboplatin/gemcitabine as initial treatment. For patients who have PD-L1-negative tumors, chemotherapy alone is used, without immunotherapy. ASTX727 is a combination of two drugs, decitabine and cedazuridine. Cedazuridine is in a class of medications called cytidine deaminase inhibitors. It prevents the breakdown of decitabine, making it more available in the body so that decitabine will have a greater effect. Decitabine is in a class of medications called hypomethylation agents. It works by helping the bone marrow produce normal blood cells and by killing abnormal cells in the bone marrow. Paclitaxel is in a class of medications called antimicrotubule agents. It stops tumor cells from growing and dividing and may kill them. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Giving ASTX727 with usual treatment approach with paclitaxel and pembrolizumab may be able to shrink or stabilize the tumor for longer than the usual approach alone in patients with metastatic triple negative breast cancer.
Key Dates
- Start date
- Sep 25, 2023
- Status verified
- Mar 2026
- Primary completion
- Feb 23, 2027
- Completion
- Feb 23, 2027
Study Design
- Enrollment
- 32 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Treatment (ASTX727, paclitaxel, pembrolizumab)Patients receive ASTX727 PO on days 1-5, 1-4, 1-3, or days 1, 3, and 5 of each cycle, and paclitaxel IV over 1 hour on days 1, 8, and 15 of each 28-day cycle or days 1 and 8 of each 21-day cycle. Cycles repeat every 21 or 28 days in the absence of disease progression or unacceptable toxicity. Patients also receive pembrolizumab IV over 30 minutes every 6 weeks (treatment day varies in 28-day cycles; day 1 of every odd 21-day cycle) in the absence of disease progression or unacceptable toxicity. Patients undergo collection of blood samples and CT and/or MRI throughout the trial. Patients in the dose-expansion phase also undergo a tumor biopsy during screening and day 1 of the treatment cycle 2 of the study.
Primary Outcome Measure
Maximally tolerated dose (MTD) of ASTX727 in combination with paclitaxel and pembrolizumab (MK-3475) (Dose Finding Phase) [ Time Frame: Within the first cycle of treatment (28 days) ]
Locations (10)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Mayo Clinic Hospital in Arizona | Phoenix | Arizona | 85054 | Site Public Contact 855-776-0015 Roberto A. Leon-Ferre (PRINCIPAL_INVESTIGATOR) |
| UC Irvine Health Cancer Center-Newport | Costa Mesa | California | 92627 | Site Public Contact 877-827-8839 Ritesh Parajuli (PRINCIPAL_INVESTIGATOR) |
| UC Irvine Health/Chao Family Comprehensive Cancer Center | Orange | California | 92868 | Ritesh Parajuli (PRINCIPAL_INVESTIGATOR) |
| University of California Davis Comprehensive Cancer Center | Sacramento | California | 95817 | - |
| Mayo Clinic in Florida | Jacksonville | Florida | 32224-9980 | Site Public Contact 855-776-0015 Roberto A. Leon-Ferre (PRINCIPAL_INVESTIGATOR) |
| Mayo Clinic in Rochester | Rochester | Minnesota | 55905 | Site Public Contact 855-776-0015 Roberto A. Leon-Ferre (PRINCIPAL_INVESTIGATOR) |
| Ohio State University Comprehensive Cancer Center | Columbus | Ohio | 43210 | Dionisia Quiroga (PRINCIPAL_INVESTIGATOR) |
| University of Oklahoma Health Sciences Center | Oklahoma City | Oklahoma | 73104 | Wajeeha Razaq (PRINCIPAL_INVESTIGATOR) |
| University of Pittsburgh Cancer Institute (UPCI) | Pittsburgh | Pennsylvania | 15232 | Site Public Contact 412-647-8073 Julia Foldi (PRINCIPAL_INVESTIGATOR) |
| VCU Massey Comprehensive Cancer Center | Richmond | Virginia | 23298 | Mary H. Hackney (PRINCIPAL_INVESTIGATOR) |
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