Efficacy and Safety of Sacituzumab Govitecan in Patients With Advanced Solid Tumors (TROPiCS-03): Analysis in Patients With Advanced Endometrial Cancer

Author:

Santin Alessandro D.1ORCID,Corr Bradley R.2ORCID,Spira Alexander3ORCID,Willmott Lyndsay4,Butrynski James5,Tse Ka Yu6ORCID,Patel Jilpa7,Mekan Sabeen7,Wu Tia7,Lin Kai-Wen7ORCID,Kuo Peiwen7ORCID,Dumbrava Ecaterina E.8ORCID

Affiliation:

1. Yale School of Medicine, New Haven, CT

2. University of Colorado Cancer Center, Aurora, CO

3. Virginia Cancer Specialists, Fairfax, VA

4. HonorHealth Virginia G. Piper Cancer Care Network Biltmore, Phoenix, AZ

5. Willamette Valley Cancer Institute and Research Center, Eugene, OR

6. School of Clinical Medicine, The University of Hong Kong, Hong Kong, China

7. Gilead Sciences, Inc, Foster City, CA

8. The University of Texas MD Anderson Cancer Center, Houston, TX

Abstract

PURPOSE Patients with advanced endometrial cancer (EC) who progress on or after platinum-based therapy and immunotherapy have poor prognosis. We report efficacy and safety of sacituzumab govitecan (SG), a trophoblast cell-surface antigen 2 (Trop-2)–directed antibody-drug conjugate, in patients with advanced EC. METHODS TROPiCS-03 (ClinicalTrials.gov identifier: NCT03964727 ) is a multicohort, open-label, phase II basket study in patients with metastatic solid tumors. Eligible patients in the EC cohort received SG 10 mg/kg once on days 1 and 8 every 3 weeks. Primary end point was objective response rate (ORR) by investigator's assessment per RECIST v1.1. Secondary end points included clinical benefit rate (CBR; complete and partial response, and stable disease ≥6 months), duration of response (DOR), and progression-free survival (PFS) per investigator assessment, overall survival, and safety. Trop-2 expression of archival or baseline tumor specimens was analyzed by immunohistochemistry. RESULTS At data extraction date, 41 patients were enrolled. Median follow-up was 5.8 months (range, 0.7-19.3); median previous therapies was three (range, 1-6); and 85% of patients received previous chemotherapy and immunotherapy. ORR was 22% (95% CI, 11 to 38); CBR was 32% (95% CI, 18 to 48). Median DOR was 8.8 months (95% CI, 2.8 to not estimable); median PFS was 4.8 months (95% CI, 2.8 to 9.8). Trop-2 exploratory analysis was conducted retrospectively for 39 patients. Tumor Trop-2 protein was highly expressed in EC, showing limited correlation with efficacy. Grade ≥3 treatment-related adverse events (TRAEs) occurred in 73% of patients. Study drug discontinuation due to TRAEs was 5%. Two deaths occurred, deemed unrelated to SG. CONCLUSION Findings from TROPiCS-03 showed encouraging efficacy of SG with a manageable toxicity profile in a heavily pretreated population with advanced EC. Safety findings were consistent with the known SG safety profile.

Publisher

American Society of Clinical Oncology (ASCO)

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