A Phase 2 Study of Sotigalimab, a CD40 Agonist Antibody, plus Concurrent Chemoradiation as Neoadjuvant Therapy for Esophageal and Gastroesophageal Junction Cancers

The current study represents the first report to evaluate a CD40 agonist antibody in combination with concurrent chemoradiation in the neoadjuvant setting for patients with esophageal/GEJ cancers. This novel strategy was both safe and feasible, producing encouraging path CR rates that compare favorably with historical data. Our findings support the further evaluation of how immune-based therapies may be incorporated into perioperative treatment paradigms for upper gastrointestinal malignancies.

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Publication Details

Journal
Cancer Research Communications
Published
2025-02-01
DOI
https://doi.org/10.1158/2767-9764.crc-24-0513
Citations
4
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
4.18
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article

A Phase 2 Study of Sotigalimab, a CD40 Agonist Antibody, plus Concurrent Chemoradiation as Neoadjuvant Therapy for Esophageal and Gastroesophageal Junction Cancers

Bridget P. Keenan, Joseph Chao, Andrew Ko, Autumn J. McRee et al.
4 citations
Cancer Research Communications
Cancer Immunotherapy and Biomarkers
4.18
article

A Phase 2 Study of Sotigalimab, a CD40 Agonist Antibody, plus Concurrent Chemoradiation as Neoadjuvant Therapy for Esophageal and Gastroesophageal Junction Cancers

Bridget P. Keenan, Joseph Chao, Andrew Ko, Autumn J. McRee, Paul E. Oberstein, Veena Shankaran, Aaron J. Scott, Xiaodong Yang, Frank J. Hsu, Marcus Smith Noel, Erin L. Filbert, Davendra Sohal, Caio Max Sao Pedro Rocha Lima, Mary Crow, Lawrence H. Fong
article en
4 citations

Abstract

The current study represents the first report to evaluate a CD40 agonist antibody in combination with concurrent chemoradiation in the neoadjuvant setting for patients with esophageal/GEJ cancers. This novel strategy was both safe and feasible, producing encouraging path CR rates that compare favorably with historical data. Our findings support the further evaluation of how immune-based therapies may be incorporated into perioperative treatment paradigms for upper gastrointestinal malignancies.

Cancer Research CommunicationsVol. 5(2)
University of North Carolina at Chapel Hill (US), Atrium Health Wake Forest Baptist (US), Johnson & Johnson (United States) (US), University of Arizona (US), University of California, San Francisco (US), Georgetown University (US), University of Washington (US), NYU Langone Health (US), City of Hope (US), Apexigen (United States) (US), Boston Public Schools (US), Texas Orthopedic Hospital (US), Wake Forest Baptist Comprehensive Cancer Center, University of Arizona Cancer Center, University of Cincinnati (US)
Good health and well-being
Openalex Percentile: Top 6%
Cancer Immunotherapy and Biomarkers
4.18
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