Abstract B006: Exploiting Myeloid-Stromal IL1RAP as a Therapeutic Vulnerability to Improve Chemoimmunotherapy Sensitivity in Pancreatic Cancer
Abstract INTRODUCTION: Pancreatic ductal adenocarcinoma (PDAC) remains highly resistant to chemotherapy and immunotherapy due to a tumor microenvironment (TME) dominated by myeloid-stromal immunosuppressive circuitries and T-cell dysfunction. Key mediators of this chemoimmunoresistance are interleukin-1 (IL-1) family cytokines (IL-1α/β, IL-33, IL-36), which converge on IL-1 receptor accessory protein (IL1RAP) signaling to reinforce a tolerogenic, proinflammatory TME. We hypothesized that IL1RAP-expressing myeloid-stromal compartments sustain a therapeutic barrier in PDAC, and that disrupting this via pharmacologic IL1RAP inhibition could reprogram the TME to enhance chemoimmunotherapy efficacy. METHODS: Chemoresistance in PDAC samples from Human Tumor Atlas Network (HTAN) was stratified by cell-type IL1RAP expression. Clinical outcomes in patients treated with anti-IL1RAP Ab nadunolimab (Nadu)+gemcitabine+nab-paclitaxel (GnP) in Phase II CANFOUR trial (NCT03267316) were stratified by immune and stromal IL1RAP expression; paired PDAC biopsies pre-/post-treatment were analyzed by mIF. Preclinical studies were conducted in the IL1RAPhi stromatogenic Ptf1aCre/+;LSL-KrasG12D;Tgfbr2fl/fl (PKT) murine model. Nadu surrogate Ab-treated tumors were analyzed by scRNAseq, flow cytometry, and histology. Combination Nadu, GnP, and anti-PD1 therapy was tested in survival studies. RESULTS: In HTAN dataset, IL1RAP expression was elevated across multiple TME compartments—myeloid, cancer-associated fibroblast (CAF), and tumor cells; notably, IL1RAP was selectively enriched in chemotherapy-resistant (vs sensitive) samples, predominantly in myeloid and CAF/stromal transcriptomes. Stratification of evaluable specimens from CANFOUR trial revealed correlation between high stromal/CAF (p=0.0058) and myeloid (p=0.014) IL1RAP expression and prolonged duration of response to Nadu+GnP. In PKT mice, Nadu treatment reduced tumor volume (p=0.019) and stromal fibrosis. Flow cytometry showed reduced trafficking/persistence (p=0.0077) and increased T-cell abundance (p=0.0033), which were corroborated by mIF in paired human PDAC biopsies pre/post Nadu treatment, showing diminished CD11b+CD14+/CD15+ myeloid infiltration and expansion of GzmB+Ki67+CD8+ T-cells. scRNAseq in PKT tumors revealed reprogramming in myeloid (↑antigen presentation and Type I IFN response; ↓IL-1/TNF signaling) and T-cell (↑activation/memory, TCR engagement, IL-2 signatures; ↓regulatory/exhausted states) subsets. Phenotypic skewing toward memory progenitor-exhausted CD8+ subsets (Ly108+CD69+/-) supported enhanced immune responsiveness. Triple therapy with Nadu, GnP, and anti-PD-1 significantly prolonged survival versus controls (p<0.001). CONCLUSIONS: IL1RAP-expressing myeloid-stromal networks may represent a distinct therapeutic barrier in PDAC, which can be disrupted pharmacologically to invigorate immunotherapy-permissive CD8+ T-cell subsets and improve chemoimmunotherapy sensitivity. These findings support an upcoming neoadjuvant trial combining nadunolimab with chemoimmunotherapy in patients with operable PDAC. Citation Format: Harper M. Marsh, Erin Dickey, Camilla Rydberg-Millrud, Haleh Amirian, Karthik Rajkumar, Luis Nivelo, Andrew Adams, Manan Patel, Elena Shersher, Siddarth Mehra, Nagaraj Nagathihalli, Emilia Oshone-Zargham Mason, Nipun Merchant, Annika Sanfridson, Anna Bianchi, David Liberg, Peter Hosein, Jashodeep Datta. Exploiting Myeloid-Stromal IL1RAP as a Therapeutic Vulnerability to Improve Chemoimmunotherapy Sensitivity in Pancreatic Cancer [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Advances in Pancreatic Cancer Research—Emerging Science Driving Transformative Solutions; Boston, MA; 2025 Sep 28-Oct 1; Boston, MA. Philadelphia (PA): AACR; Cancer Res 2025;85(18_Suppl_3):Abstract nr B006.
Authors
- Jashodeep Datta (ORCID: https://orcid.org/0000-0003-2869-1571)
- Emilia Mason
- Karthik Rajkumar (ORCID: https://orcid.org/0000-0002-3604-3657)
- Anna Bianchi (ORCID: https://orcid.org/0000-0002-5963-103X)
- Nipun B. Merchant (ORCID: https://orcid.org/0000-0002-3399-9776)
- Nagaraj S. Nagathihalli (ORCID: https://orcid.org/0000-0003-2373-3293)
- Annika Sanfridson (ORCID: https://orcid.org/0000-0001-6725-7562)
- Andrew Adams (ORCID: https://orcid.org/0009-0006-0102-3062)
- Siddharth Mehra (ORCID: https://orcid.org/0000-0003-1639-8087)
- Peter J. Hosein (ORCID: https://orcid.org/0000-0001-8537-6397)
- Elena Shersher
- Camilla Rydberg-Millrud
- Haleh Amirian (ORCID: https://orcid.org/0000-0002-6094-1342)
- Luis Nivelo (ORCID: https://orcid.org/0000-0002-4943-1827)
- Erin M. Dickey
- Manan Patel (ORCID: https://orcid.org/0000-0001-6978-960X)
- David Liberg (ORCID: https://orcid.org/0009-0009-0645-746X)
- Howard Marsh
Institutions
- Baptist Hospital of Miami (US)
- University of Miami (US)
- ABS Consulting (United States) (US)
Publication Details
- Journal
- Cancer Research
- Published
- 2025-09-28
- DOI
- https://doi.org/10.1158/1538-7445.pancreatic25-b006
- Primary Topic
- Immune cells in cancer
- Type
- article
- Field-Weighted Citation Impact
- 0.00