At a glance
ClinicalIndex Comparison Record- ✓Pathologically confirmed residual invasive breast cancer in breast and/or lymph nodes post-neoadjuvant chemotherapy
- ✓HER2 negative by ISH or IHC 0/1+
- ✓ER and PR negative (<10% of cells) by IHC
- ✓Prior neoadjuvant chemotherapy before breast surgery
- ✕Prior therapy with sacituzumab govitecan, irinotecan, or topoisomerase I-containing antibody-drug conjugates
- ✕Receipt of adjuvant chemotherapy
- ✕Clinical or radiographic evidence of metastatic disease
- ✕Residual DCIS or LCIS alone or pT0N0i and pT0N1mic disease
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Single Arm Phase 2 Trial of Atezolizumab With Sacituzumab Govitecan to Prevent Recurrence in Triple Negative Breast Cancer (ASPRIA)
In Brief
A Phase 2 clinical trial evaluating Atezolizumab and Sacituzumab govitecan for Breast Cancer and 3 related conditions. Currently recruiting, targeting 40 participants across 7 sites.
Detailed Summary
The purpose of this study is to determine if a combination of two drugs sacituzumab govitecan and atezolizumab works as a treatment for residual cancer in the breast or lymph nodes and have circulating tumor DNA in the blood. This research study involves the following investigational drugs: * Sacituzumab govitecan * Atezolizumab
Study Details
Timeline
Interventions
Atezolizumab is a type of antibody and is administered intravenously.
Sacituzumab govitecan is an antibody drug conjugate and is administered intravenously