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Cytometric Atlas of Combination Immunotherapy in Pancreatic Cancer: Blood-Based Signatures Reveal Vaccine and Checkpoint Inhibitor Responses.

Cancer immunology research 2026 Vol.14(3) p. 399-410

Sidiropoulos DN, Zhang Z, Durham JN, Charmsaz S, Gross NE, Lee JW, Sun Y, Perikala S, Tandurella JA, Lvovs D, Mitschang A, Lemson G, Shin SM, Hernandez AG, Mitchell S, Leatherman JM, Danilova L, Wang H, Fertig EJ, Jaffee EM, Bever KM, Le DT, Ho WJ

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Combination vaccine and checkpoint inhibitor therapy has previously demonstrated immunologic responses in patients with pancreatic ductal adenocarcinoma (PDAC), although with limited efficacy.

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BibTeX ↓ RIS ↓
APA Sidiropoulos DN, Zhang Z, et al. (2026). Cytometric Atlas of Combination Immunotherapy in Pancreatic Cancer: Blood-Based Signatures Reveal Vaccine and Checkpoint Inhibitor Responses.. Cancer immunology research, 14(3), 399-410. https://doi.org/10.1158/2326-6066.CIR-25-1126
MLA Sidiropoulos DN, et al.. "Cytometric Atlas of Combination Immunotherapy in Pancreatic Cancer: Blood-Based Signatures Reveal Vaccine and Checkpoint Inhibitor Responses.." Cancer immunology research, vol. 14, no. 3, 2026, pp. 399-410.
PMID 41524578

Abstract

Combination vaccine and checkpoint inhibitor therapy has previously demonstrated immunologic responses in patients with pancreatic ductal adenocarcinoma (PDAC), although with limited efficacy. An urgent need to augment responses has warranted a deeper understanding of how each treatment modality contributes to the overall inflammatory response. Serial blood samples from patients with PDAC treated with GVAX, CRS-207, anti-CTLA-4, and/or anti-PD-1 therapies were profiled using two mass cytometry panels. Generating 260 cytometric profiles from 64 unique patients allowed us to create an annotated PDAC immunotherapy atlas. Analysis of this atlas revealed that although GVAX alone did not significantly alter T-cell relative frequencies, it induced T-cell activation and upregulated checkpoint expression. Adding anti-PD-1 blockade to GVAX further enhanced T-cell activation, whereas adding anti-CTLA-4 distinctly enhanced memory formation. Vaccine-mediated effects were similar, but GVAX promoted plasmacytoid dendritic cells more than CRS-207. Derived phenotypic patterns could also be projected onto tumor imaging data, underscoring the potential for discoveries relating treatment-induced peripheral signatures to changes in the tumor microenvironment. See related article by Bever et al., p. 411.

MeSH Terms

Humans; Pancreatic Neoplasms; Immune Checkpoint Inhibitors; Cancer Vaccines; Immunotherapy; Carcinoma, Pancreatic Ductal; Tumor Microenvironment; Female; Male; Combined Modality Therapy; Flow Cytometry; Middle Aged; Aged

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