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

IF 42.1 1区 医学 Q1 ONCOLOGY
Journal of Clinical Oncology Pub Date : 2024-10-10 Epub Date: 2024-07-31 DOI:10.1200/JCO.23.02767
Alessandro D Santin, Bradley R Corr, Alexander Spira, Lyndsay Willmott, James Butrynski, Ka Yu Tse, Jilpa Patel, Sabeen Mekan, Tia Wu, Kai-Wen Lin, Peiwen Kuo, Ecaterina E Dumbrava
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引用次数: 0

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.

萨妥珠单抗戈维替康对晚期实体瘤患者的疗效和安全性(TROPiCS-03):晚期子宫内膜癌患者分析。
目的:晚期子宫内膜癌(EC)患者在接受铂类治疗和免疫治疗后病情进展,预后较差。我们报告了滋养层细胞表面抗原2(Trop-2)导向的抗体-药物共轭物sacituzumab govitecan(SG)在晚期子宫内膜癌患者中的疗效和安全性:TROPiCS-03(ClinicalTrials.gov标识符:NCT03964727)是一项针对转移性实体瘤患者的多队列、开放标签、II期篮子研究。符合条件的EC队列患者在第1天和第8天接受SG 10 mg/kg,每3周一次。主要终点是研究者根据 RECIST v1.1 评估的客观反应率(ORR)。次要终点包括临床获益率(CBR;完全和部分应答,疾病稳定≥6个月)、应答持续时间(DOR)、研究者评估的无进展生存期(PFS)、总生存期和安全性。通过免疫组化分析档案或基线肿瘤标本中Trop-2的表达情况:截至数据提取日,共有41名患者入组。中位随访时间为5.8个月(0.7-19.3个月);中位既往治疗时间为3个月(1-6个月);85%的患者接受过化疗和免疫治疗。ORR为22%(95% CI,11-38);CBR为32%(95% CI,18-48)。中位DOR为8.8个月(95% CI,2.8至无法估计);中位PFS为4.8个月(95% CI,2.8至9.8)。对39名患者进行了Trop-2探索性分析。肿瘤Trop-2蛋白在EC中高表达,但与疗效的相关性有限。73%的患者发生了≥3级治疗相关不良事件(TRAE)。因 TRAEs 而停药的患者占 5%。有2例死亡病例被认为与SG无关:TROPiCS-03的研究结果表明,SG在晚期EC重度预处理人群中具有令人鼓舞的疗效和可控的毒性。安全性研究结果与已知的 SG 安全性特征一致。
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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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