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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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Cancer cell 📖 저널 OA 38.1% 2024: 2/4 OA 2025: 7/18 OA 2026: 15/41 OA 2024~2026 2026 Vol.44(4) p. 846-857.e3 cited 2 OA Lung Cancer Treatments and Mutations
TL;DR Results support further development of HS-20093, with 8.0 mg/kg selected for phase 3 trials, with 8.0 mg/kg established as the maximum tolerated dose.
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PubMed DOI OpenAlex Semantic 마지막 보강 2026-04-30
OpenAlex 토픽 · Lung Cancer Treatments and Mutations HER2/EGFR in Cancer Research Peptidase Inhibition and Analysis

Duan J, Sun Y, Wang Q, Xing L, Wu L, Han L, Chen J, Liu B, Lu P, Shi H, Yu X, Zhang J, Zhang G, Hu Y, Cheng Y, Sun H, Yang H, Zhang Z, Ning F, He Z, Yao W, Dong Y, Zhang M, Song B, Zhou Y, Mao X, Liu Q, Wang J

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Results support further development of HS-20093, with 8.0 mg/kg selected for phase 3 trials, with 8.0 mg/kg established as the maximum tolerated dose.

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  • 표본수 (n) 65

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APA Jianchun Duan, Yuping Sun, et al. (2026). HS-20093, a B7-H3-targeted antibody-drug conjugate in lung cancer: Results from the ARTEMIS-001 phase 1a/b trial.. Cancer cell, 44(4), 846-857.e3. https://doi.org/10.1016/j.ccell.2026.02.006
MLA Jianchun Duan, et al.. "HS-20093, a B7-H3-targeted antibody-drug conjugate in lung cancer: Results from the ARTEMIS-001 phase 1a/b trial.." Cancer cell, vol. 44, no. 4, 2026, pp. 846-857.e3.
PMID 41791381 ↗

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.

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