HS-20093, a B7-H3-targeted antibody-drug conjugate in lung cancer: Results from the ARTEMIS-001 phase 1a/b trial

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Authors: Jianchun Duan, Yuping Sun, Qiming Wang, Ligang Xing, Lin Wu, Liang Han, Jianhua Chen, Baogang Liu, Ping Lu, Huaqiu Shi, Xinmin Yu, Junhong Zhang
+16 more Guoping Zhang, Yanping Hu, Ying Cheng, Hongmei Sun, Haihua Yang, Zhiye Zhang, Fangling Ning, Zhiyong He, WenXiu Yao, Yiwei Dong, Min Zhang (111999), Baili Song, Yuanfeng Zhou, Xiangru Mao, Qingyuan Liu, Jie Wang
Cited by: 17
References: 21

Abstract

This phase 1a/b study (NCT05276609) evaluated the safety, pharmacokinetics, and efficacy of B7-H3-targeted antibody-drug conjugate HS-20093 (GSK5764227) in 306 patients with previously treated advanced solid tumors. In phase 1a, 12.0 mg/kg was established as the maximum tolerated dose. Among 236 lung cancer patients who received 8.0 or 10.0 mg/kg HS-20093, the most frequent grade ≥3 treatment-related adverse events (AEs) included decreased neutrophil (25.5% vs. 50.5%) and white blood cell counts (19.7% vs. 42.4%), and anemia (16.8% vs. 34.3%), respectively. Treatment-related interstitial lung disease and AEs leading to death occurred in 3.4% and 3.8% of patients, respectively. Among response-evaluable patients, the confirmed objective response rate was 52.3% (95% CI: 39.5, 64.9) for extensive-stage SCLC (ES-SCLC, N = 65) and 22.4% (95% CI: 16.0, 29.8) for non-small cell lung cancer (NSCLC, N = 152) patients, with comparable rates between 8.0 mg/kg and 10.0 mg/kg dose cohorts across both groups. These results support further development of HS-20093, with 8.0 mg/kg selected for phase 3 trials.

Fields of Study & Subjects

Lung Cancer Treatments and Mutations HER2/EGFR in Cancer Research Peptidase Inhibition and Analysis

Publication details

Journal / source
Cancer Cell
Publisher
Elsevier BV
Volume
44
Issue
4
Pages
846–857.e3
Publication date
5 March 2026
Language
EN