Publications
245
Citations
6,357
Est. group size
—
Recurring co-author estimate
Active years
36
Publishing since 1991
Scott A. Hammond's work focuses on cancer immunotherapy, studying how the immune system interacts with tumors and how treatments like checkpoint inhibitors (drugs blocking proteins such as PD-1/PD-L1) and engineered antibody or T-cell-based therapies can be used to fight cancer. Recent research includes analyzing why some tumors develop resistance to immunotherapy, testing new antibody-based drugs in cancer models, and studying immune cells within tumors such as macrophages. This research is largely translational, combining laboratory models with real-world patient data to understand and improve cancer immunotherapies.
Publication output was modest and variable from 2017-2022 but rose sharply starting in 2023, with a large spike that year followed by continued elevated output through 2025, suggesting a recent period of substantially increased research activity.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Pan-cancer analysis in the real-world setting uncovers immunogenomic drivers of acquired resistance post-immunotherapy
Journal for ImmunoTherapy of Cancer · 2026
- Abstract 5546: Rilvegostomig elicits greater immune activation and tumor inhibition than clinically approved anti-PD-1 monotherapy in models of HNSCC
Cancer Research · 2026
- An affinity-modulated T cell engager targeting Claudin 18.2 shows potent anti-tumor activity with limited cytokine release
Journal for ImmunoTherapy of Cancer · 2025
- <i>In Vivo</i> Labeling Resolves Distinct Temporal, Spatial, and Functional Properties of Tumor Macrophages and Identifies Subset-Specific Effects of PD-L1 Blockade
Cancer Immunology Research · 2025
- DEVELOPMENT OF EX VIVO PATIENT-DERIVED MODELS TO UNCOVER THE TUMOR-IMMUNE MICROENVIRONMENT IN RENAL CELL CARCINOMA
Urologic Oncology Seminars and Original Investigations · 2025
- Pan-Cancer Analysis in the Real-World Setting Uncovers Immunogenomic Drivers of Acquired Resistance Post-Immunotherapy
SSRN Electronic Journal · 2025
- Figure S8 from <i>In Vivo</i> Labeling Resolves Distinct Temporal, Spatial, and Functional Properties of Tumor Macrophages and Identifies Subset-Specific Effects of PD-L1 Blockade
2025
- Figure S2 from <i>In Vivo</i> Labeling Resolves Distinct Temporal, Spatial, and Functional Properties of Tumor Macrophages and Identifies Subset-Specific Effects of PD-L1 Blockade
2025
- Figure S7 from <i>In Vivo</i> Labeling Resolves Distinct Temporal, Spatial, and Functional Properties of Tumor Macrophages and Identifies Subset-Specific Effects of PD-L1 Blockade
2025
- Figure S3 from <i>In Vivo</i> Labeling Resolves Distinct Temporal, Spatial, and Functional Properties of Tumor Macrophages and Identifies Subset-Specific Effects of PD-L1 Blockade
2025
- Figure S9 from <i>In Vivo</i> Labeling Resolves Distinct Temporal, Spatial, and Functional Properties of Tumor Macrophages and Identifies Subset-Specific Effects of PD-L1 Blockade
2025
- Figure S1 from <i>In Vivo</i> Labeling Resolves Distinct Temporal, Spatial, and Functional Properties of Tumor Macrophages and Identifies Subset-Specific Effects of PD-L1 Blockade
2025
- Figure S6 from <i>In Vivo</i> Labeling Resolves Distinct Temporal, Spatial, and Functional Properties of Tumor Macrophages and Identifies Subset-Specific Effects of PD-L1 Blockade
2025
- Figure S4 from <i>In Vivo</i> Labeling Resolves Distinct Temporal, Spatial, and Functional Properties of Tumor Macrophages and Identifies Subset-Specific Effects of PD-L1 Blockade
2025
- Supplementary table 1 from <i>In Vivo</i> Labeling Resolves Distinct Temporal, Spatial, and Functional Properties of Tumor Macrophages and Identifies Subset-Specific Effects of PD-L1 Blockade
2025
- Regular and Young Investigator Award Abstracts×16
- Cancer Research×9
- UNC Libraries×5
- Journal for ImmunoTherapy of Cancer×4
- Cancer Immunology Research×3
- Joseph Azar
Medicine · The Ohio State University
- No‐Joon Song
Medicine · The Ohio State University
- Andreas Wieland
Medicine · The Ohio State University
- Tarah J. Ballinger
Medicine · Indiana University
- Yoshinobu Koguchi
Medicine · The Ohio State University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 19, 2026.
Claim or correct this profile