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.

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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
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article

Phase I study of allogeneic monocyte-derived inflammatory dendritic cells in combination with pembrolizumab

Alex Karlsson‐Parra, John Hamm, David J. Bajor, Douglas Laux et al.
Future Science OA
Cancer Immunotherapy and Biomarkers
article

Phase I study of allogeneic monocyte-derived inflammatory dendritic cells in combination with pembrolizumab

Alex Karlsson‐Parra, John Hamm, David J. Bajor, Douglas Laux, A. Craig Lockhart, Jared Weiss, Jeroen Rovers
article en

Abstract

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.

Future Science OAVol. 10(1)
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)
Openalex Percentile: Top 63%
Cancer Immunotherapy and Biomarkers
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