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

被引:6
|
作者
Santin, Alessandro D. [1 ]
Corr, Bradley R. [2 ]
Spira, Alexander [3 ]
Willmott, Lyndsay [4 ]
Butrynski, James [5 ]
Tse, Ka Yu [6 ]
Patel, Jilpa [7 ]
Mekan, Sabeen [7 ]
Wu, Tia [7 ]
Lin, Kai-Wen [7 ]
Kuo, Peiwen [7 ]
Dumbrava, Ecaterina E. [8 ]
机构
[1] Yale Sch Med, New Haven, CT 06510 USA
[2] Univ Colorado, Canc Ctr, Aurora, CO USA
[3] Virginia Canc Specialists, Fairfax, VA USA
[4] HonorHealth Virginia G Piper Canc Care Network Bil, Phoenix, AZ USA
[5] Willamette Valley Canc Inst & Res Ctr, Eugene, OR USA
[6] Univ Hong Kong, Sch Clin Med, Hong Kong, Peoples R China
[7] Gilead Sci Inc, Foster City, CA USA
[8] Univ Texas MD Anderson Canc Ctr, Houston, TX USA
关键词
ANTIBODY-DRUG CONJUGATE; CONFIDENCE; TROP-2;
D O I
10.1200/JCO.23.02767
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSEPatients 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.METHODSTROPiCS-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.RESULTSAt 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.CONCLUSIONFindings 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.
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页数:11
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