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. 2024 Jun 30;15(3):1348-1354.
doi: 10.21037/jgo-24-71. Epub 2024 Jun 20.

Hepatic artery infusion pump (HAIP) therapy in combination with targeted delivery of IL-12 for patients with metastatic colorectal cancer or intrahepatic cholangiocarcinoma: a phase II trial protocol

Affiliations

Hepatic artery infusion pump (HAIP) therapy in combination with targeted delivery of IL-12 for patients with metastatic colorectal cancer or intrahepatic cholangiocarcinoma: a phase II trial protocol

Jack H Victory et al. J Gastrointest Oncol. .

Abstract

Background: Treatment of advanced liver tumors remains challenging. Although immune checkpoint inhibition has revolutionized treatment for many cancers, responses in colorectal liver metastases and biliary tract cancers remain suboptimal. Investigation into additional immunomodulatory therapies for these cancers is needed. Interleukin-12 (IL-12) is a pro-inflammatory cytokine with robust anti-tumor activity, but systemic adverse effects largely terminated therapeutic development of recombinant human IL-12 (rhIL-12). PDS01ADC is a novel human monoclonal antibody (NHS76) conjugated to two IL-12 heterodimers with established safety in phase I trials. The NHS76 antibody specifically targets histone/DNA complexes which are accessible only in regions of cell death and this antibody has been shown to accumulate locally in tumors.

Methods: Patients with unresectable metastatic colorectal cancer (mCRC) or unresectable intrahepatic cholangiocarcinoma (ICC) will receive synchronization of subcutaneous PDS01ADC with floxuridine delivered via a hepatic artery infusion pump (HAIP). The primary outcome measured in this study will be overall response rate as measured by Response Evaluation Criteria in Solid Tumors (RECIST) criteria. Secondary outcomes measured in this study will include hepatic and non-hepatic progression-free survival (PFS), overall survival, and safety of PDS01ADC combination therapy with HAIP.

Discussion: Poor clinical response of these liver tumors to immunotherapy is likely due to various factors, including poor immune infiltrate into the tumor and immunosuppression by the tumor microenvironment. By exploiting the tumor cell death induced by HAIP locoregional therapy in combination with systemic chemotherapy, PDS01ADC is poised to modulate the tumor immune microenvironment to improve outcomes for patients undergoing HAIP therapy.

Trial registration: ClinicalTrials.gov (ID NCT05286814 version 2023-10-18); https://clinicaltrials.gov/study/NCT05286814?term=NCT05286814&rank=1.

Keywords: Metastatic colorectal cancer (mCRC); floxuridine; hepatic artery infusion pump (HAIP); interleukin-12 (IL-12); intrahepatic cholangiocarcinoma (ICC).

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Conflict of interest statement

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://jgo.amegroups.com/article/view/10.21037/jgo-24-71/coif). J.S. reports receiving funding from a National Cancer Institute Cooperative Research and Development Agreement (CRADA) with PDS Biotechnology regarding NHS-IL12. The other authors have no conflicts of interest to declare.

Figures

Figure 1
Figure 1
Summary of trial study population, treatment dosing schedule, and objectives to be measured in the study. Created with BioRender.com. FUDR, floxuridine; FOLFOX, leucovorin, 5-fluorouracil, and oxaliplatin; FOLFIRI, leucovorin, 5-fluorouracil, and irinotecan; GemOx, gemcitabine and oxaliplatin; HAIP, hepatic artery infusion pump; s.c., subcutaneous; i.v., intravenous.

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