B7-H4‒directed antibody-drug conjugate AZD8205 (puxitatug samrotecan) in patients with advanced/metastatic solid tumors: the Phase 1/2a (BLUESTAR), first-in-human study

B7-H4 is a promising antibody-drug conjugate (ADC) target with high expression in several solid tumors and limited expression in normal tissue. B7-H4 negatively regulates T-cell function, and high expression of B7-H4 is associated with disease progression. AZD8205 (puxitatug samrotecan [Puxi-Sam]) is a novel B7-H4–directed ADC with a stable cleavable linker and a bystander-capable topoisomerase-1 (TOP1) inhibitor payload. In this first-in-human study, 47 patients with advanced/metastatic B7-H4−positive endometrial cancer, ovarian cancer, breast cancer or cholangiocarcinoma received intravenous Puxi-Sam at 0.8–3.2 mg/kg every 3 weeks. The primary objectives were to evaluate the safety and tolerability of Puxi-Sam (incidence of adverse events [AE], serious AEs and dose-limiting toxicities), and to determine the maximum tolerated dose and/or recommended phase 2 dose of Puxi-Sam. Secondary objectives included characterizing the pharmacokinetics, assessing the antitumor activity (objective response rate [ORR]), and determining the pharmacodynamics of Puxi-Sam. The most common treatment-related adverse events were nausea (51.1%), neutropenia (48.9%) and anemia (38.3%). At 3.2 mg/kg, dose-limiting neutropenia and thrombocytopenia were observed. In patients treated at ≥1.6 mg/kg (predicted efficacious range), partial responses were observed in ovarian, endometrial and breast cancer (ORR 20.5% [9/44]). Translational data indicated selective localization of the TOP1 inhibitor payload to B7-H4–expressing tumor cells and induction of target-dependent DNA damage. Our findings demonstrate manageable safety and promising efficacy with Puxi-Sam in heavily pretreated patients; further development is ongoing. ClinicalTrials.gov: NCT05123482. B7-H4 is a promising therapeutic target in solid tumors because of its frequent expression in cancer cells, limited normal tissue distribution, and immunosuppressive functions. In this first-in-human trial, the authors report safety and efficacy outcomes for B7-H4–directed antibody-drug conjugate AZD8205 (puxitatug samrotecan) in patients with heavily pretreated ovarian, endometrial, and breast cancers, and cholangiocarcinoma.

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Nature Communications
Published
2026-10-30
DOI
https://doi.org/10.1038/s41467-026-78925-8
Primary Topic
Cancer Immunotherapy and Biomarkers
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article
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article

B7-H4‒directed antibody-drug conjugate AZD8205 (puxitatug samrotecan) in patients with advanced/metastatic solid tumors: the Phase 1/2a (BLUESTAR), first-in-human study

Theresa A. Proia, Tatsunori Shimoi, Andrew A. Davis, Vincent M. Chung et al.
7 links
Nature Communications
Cancer Immunotherapy and Biomarkers
article

B7-H4‒directed antibody-drug conjugate AZD8205 (puxitatug samrotecan) in patients with advanced/metastatic solid tumors: the Phase 1/2a (BLUESTAR), first-in-human study

Theresa A. Proia, Tatsunori Shimoi, Andrew A. Davis, Vincent M. Chung, Stephanie L. Gaillard, Vincent F. S. Dubois, Jixin Wang, Mary McFarlane, Do‐Youn Oh, Linda Mileshkin, Yoichi Naito, Nadia Luheshi, Funda Meric‐Bernstam, Marlon Cezar Rebelatto, Neil R. Miller, Jun Tian, Shreyas Upadhyay, Andreea Varga, Minal Kulkarni
article en

Abstract

B7-H4 is a promising antibody-drug conjugate (ADC) target with high expression in several solid tumors and limited expression in normal tissue. B7-H4 negatively regulates T-cell function, and high expression of B7-H4 is associated with disease progression. AZD8205 (puxitatug samrotecan [Puxi-Sam]) is a novel B7-H4–directed ADC with a stable cleavable linker and a bystander-capable topoisomerase-1 (TOP1) inhibitor payload. In this first-in-human study, 47 patients with advanced/metastatic B7-H4−positive endometrial cancer, ovarian cancer, breast cancer or cholangiocarcinoma received intravenous Puxi-Sam at 0.8–3.2 mg/kg every 3 weeks. The primary objectives were to evaluate the safety and tolerability of Puxi-Sam (incidence of adverse events [AE], serious AEs and dose-limiting toxicities), and to determine the maximum tolerated dose and/or recommended phase 2 dose of Puxi-Sam. Secondary objectives included characterizing the pharmacokinetics, assessing the antitumor activity (objective response rate [ORR]), and determining the pharmacodynamics of Puxi-Sam. The most common treatment-related adverse events were nausea (51.1%), neutropenia (48.9%) and anemia (38.3%). At 3.2 mg/kg, dose-limiting neutropenia and thrombocytopenia were observed. In patients treated at ≥1.6 mg/kg (predicted efficacious range), partial responses were observed in ovarian, endometrial and breast cancer (ORR 20.5% [9/44]). Translational data indicated selective localization of the TOP1 inhibitor payload to B7-H4–expressing tumor cells and induction of target-dependent DNA damage. Our findings demonstrate manageable safety and promising efficacy with Puxi-Sam in heavily pretreated patients; further development is ongoing. ClinicalTrials.gov: NCT05123482. B7-H4 is a promising therapeutic target in solid tumors because of its frequent expression in cancer cells, limited normal tissue distribution, and immunosuppressive functions. In this first-in-human trial, the authors report safety and efficacy outcomes for B7-H4–directed antibody-drug conjugate AZD8205 (puxitatug samrotecan) in patients with heavily pretreated ovarian, endometrial, and breast cancers, and cholangiocarcinoma.

Nature Communications
AstraZeneca (United Kingdom) (GB), City Of Hope National Medical Center (US), The University of Texas MD Anderson Cancer Center (US), Seoul National University (KR), Johns Hopkins University (US), Washington University in St. Louis (US), Johns Hopkins Medicine (US), Peter MacCallum Cancer Centre (AU), Seoul National University Hospital (KR), City of Hope (US), National Cancer Center Hospital East (JP), Johns Hopkins Hospital (US), AstraZeneca (United States) (US), National Cancer Center Hospital (JP)
AstraZeneca
Good health and well-being
Openalex Percentile: Top 16%
Cancer Immunotherapy and Biomarkers
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