Phase I study of allogeneic monocyte-derived inflammatory dendritic cells in combination with pembrolizumab
PD-1 checkpoint inhibition has revolutionized the care of cancer. A small portion of patients with stage IV cancer achieve durable control. But, early progression is common and dramatic control is achieved for only a minority. We hypothesized that ilixadencel, an allogeneic monocyte-derived dendritic cell product could be injected into tumor to potentiate PD-1 response and thus conducted a phase I study of pembrolizumab plus ilixadencel. Twenty-one patients were accrued. The most common treatment emergent adverse events were fatigue, injection site pain, anemia, weight decreased and hyponatremia, mostly grade 1-2. No dose limiting toxicities were observed and the recommended phase II dose was established at 10 million cells administered twice. Two unconfirmed responses were observed, with no confirmed responses.
Authors
- Alex Karlsson‐Parra (ORCID: https://orcid.org/0000-0003-1050-7908)
- John Hamm (ORCID: https://orcid.org/0000-0003-2139-8989)
- David J. Bajor
- Douglas Laux (ORCID: https://orcid.org/0000-0001-6499-3708)
- A. Craig Lockhart (ORCID: https://orcid.org/0000-0002-0132-5523)
- Jared Weiss
- Jeroen Rovers
Institutions
- University of North Carolina at Chapel Hill (US)
- Medical University of South Carolina (US)
- Norton Healthcare (US)
- University Hospitals of Cleveland (US)
- University of Iowa Hospitals and Clinics (US)
- Maryland Oncology Hematology (US)
- MUSC Hollings Cancer Center (US)
- Mentis Sciences (United States) (US)
Publication Details
- Journal
- Future Science OA
- Published
- 2024-11-20
- DOI
- https://doi.org/10.1080/20565623.2024.2426426
- Primary Topic
- Cancer Immunotherapy and Biomarkers
- Type
- article
- Field-Weighted Citation Impact
- 0.00