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.
Authors
- Theresa A. Proia (ORCID: https://orcid.org/0009-0000-4572-5118)
- Tatsunori Shimoi (ORCID: https://orcid.org/0000-0002-3603-8575)
- Andrew A. Davis (ORCID: https://orcid.org/0000-0003-3663-2133)
- Vincent M. Chung (ORCID: https://orcid.org/0000-0001-9475-808X)
- Stephanie L. Gaillard (ORCID: https://orcid.org/0000-0002-2174-3693)
- Vincent F. S. Dubois (ORCID: https://orcid.org/0000-0002-7423-5473)
- Jixin Wang (ORCID: https://orcid.org/0000-0001-7079-2056)
- Mary McFarlane (ORCID: https://orcid.org/0000-0002-1211-8650)
- Do‐Youn Oh (ORCID: https://orcid.org/0000-0003-1663-9901)
- Linda Mileshkin (ORCID: https://orcid.org/0000-0001-6826-6014)
- Yoichi Naito (ORCID: https://orcid.org/0000-0002-8490-9064)
- Nadia Luheshi (ORCID: https://orcid.org/0000-0002-4530-5188)
- Funda Meric‐Bernstam (ORCID: https://orcid.org/0000-0001-6816-6072)
- Marlon Cezar Rebelatto
- Neil R. Miller (ORCID: https://orcid.org/0009-0005-8242-3326)
- Jun Tian
- Shreyas Upadhyay
- Andreea Varga
- Minal Kulkarni
Institutions
- 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)
Publication Details
- Journal
- Nature Communications
- Published
- 2026-10-30
- DOI
- https://doi.org/10.1038/s41467-026-78925-8
- Primary Topic
- Cancer Immunotherapy and Biomarkers
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- AstraZeneca