A Randomized, Open-Label, Phase 3 Study of Adjuvant Sacituzumab Govitecan and Pembrolizumab Versus Treatment of Physician's Choice in Patients With Triple Negative Breast Cancer Who Have Residual Invasive Disease After Surgery and Neoadjuvant Therapy
Enrolling By Invitation
18-100 years
Female
Phase
3
Brief description of study
The goal of this study is to find out if the experimental product, sacituzumab govitecan-hziy (SG) in combination with pembrolizumab given after surgery, is effective and safe compared to the treatment of physician's choice (TPC) which includes either pembrolizumab or pembrolizumab plus capecitabine in participants with triple negative breast cancer that still remains after surgery and pre-surgical treatment.
Detailed description of study
This study is Enrolling by Invitation only at Lancaster General Health - ABBCI.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
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Conditions:
In clinic, in person
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Age: Between 18 Years - 100 Years
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Gender: Female
Inclusion Criteria:
- Age > 18 years, with residual invasive triple negative breast cancer (TNBC) in the breast or lymph nodes after neoadjuvant therapy and surgery: TNBC criteria for the study is defined as estrogen receptor (ER) and progesterone receptor (PR) < 10% human epidermal growth factor receptor 2 (HER2)-negative per American Society of Clinical Oncology and College of American Pathologists (ASCO/CAP) guidelines (immunohistochemistry (IHC) and/or in situ hybridization (ISH)).
- Adequate excision and surgical removal of all clinically evident of disease in the breast and/or lymph nodes and have adequately recovered from surgery
- Submission of both pre-neoadjuvant treatment diagnostic biopsy and resected residual invasive disease tissue
- Eastern Cooperative Oncology Group (ECOG) performance status 0-1
- Individuals must have received appropriate radiotherapy and have recovered prior to starting study treatment
- Adequate organ function
Exclusion Criteria:
- Stage IV (metastatic) breast cancer as well as history of any prior (ipso-or contralateral) invasive breast cancer
- Prior treatment with another stimulatory or coinhibitory T-cell receptor agent (eg, cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4), OX-40, cluster of differentiation 137 (CD137), prior treatment with any HER2-directed agent
- Evidence of recurrent disease following preoperative therapy and surgery
- Prior treatment with topoisomerase 1 inhibitors or antibody-drug conjugates (ADCs) containing a topoisomerase inhibitor
- Individuals with known germline breast cancer gene (BRCA) mutations
- Myocardial infarction or unstable angina pectoris within 6 months of enrollment or history of serious ventricular arrhythmia (ie, ventricular tachycardia or ventricular fibrillation), high-grade atrioventricular block, or other cardiac arrhythmias or Left ventricular ejection fraction (LVEF) of <50%
- Active serious infections requiring anti-microbial therapy
Updated on
01 Aug 2024.
Study ID: GS-US-595-6184
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