Abstract 4459: Repurposed FDA-approved agents for hepatic artery infusion in colorectal liver metastases.

Abstract Colorectal cancer (CRC) remains a leading cause of cancer-related death, with liver metastases (CRLM) representing the most common cause of mortality. Despite advances in systemic therapy, outcomes for patients with CRLM remain poor, underscoring a critical need for improved, liver-directed treatment strategies. Hepatic artery infusion (HAI) pumps are an effective method to deliver high local concentrations of chemotherapy directly to the liver while limiting systemic toxicity. The currently-standard of care compounds for HAI have limited efficacy and elevated hepatotoxicity, emphasizing the demand for treatment regimens that have better patient outcomes. In this project, we explored a drug repurposing strategy by evaluating FDA-approved chemotherapeutic agents with pharmacokinetic properties compatible with HAI delivery. Drugs were selected using established pharmacokinetic databases and then tested in vitro using CRC cell models and a normal epithelial liver cell line to assess cytotoxicity and dose-response. In addition, we investigated the therapeutic potential of combining a microtubule destabilizer with an FDA-approved fatty acid synthase (FASN) inhibitor. Synergy experiments demonstrated enhanced cytotoxic effects when chemotherapeutics were combined with the FASN inhibitor, suggesting that there is potential for a novel treatment regimen for patients presenting with this disease. These preliminary findings support drug repurposing within the context of HAI delivery as a clinically translatable approach. By utilizing existing FDA-approved compounds of both chemotherapeutic agents and metabolic inhibitors, this strategy may lay the groundwork for novel therapies for patients with CRLM. Further preclinical and translational studies will be necessary to define optimal drug combinations and dosing regimens, with the ultimate goal of expanding therapeutic options and improving outcomes for this high-risk patient population. Citation Format: Manasa Ravi, Colin M. Court, April Risinger. Repurposed FDA-approved agents for hepatic artery infusion in colorectal liver metastases [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 4459.

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Publication Details

Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-4459
Primary Topic
Cancer, Lipids, and Metabolism
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article
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article

Abstract 4459: Repurposed FDA-approved agents for hepatic artery infusion in colorectal liver metastases.

Colin M. Court, April L. Risinger, Manasa Ravi
Cancer Research
Cancer, Lipids, and Metabolism
article

Abstract 4459: Repurposed FDA-approved agents for hepatic artery infusion in colorectal liver metastases.

Colin M. Court, April L. Risinger, Manasa Ravi
article en

Abstract

Abstract Colorectal cancer (CRC) remains a leading cause of cancer-related death, with liver metastases (CRLM) representing the most common cause of mortality. Despite advances in systemic therapy, outcomes for patients with CRLM remain poor, underscoring a critical need for improved, liver-directed treatment strategies. Hepatic artery infusion (HAI) pumps are an effective method to deliver high local concentrations of chemotherapy directly to the liver while limiting systemic toxicity. The currently-standard of care compounds for HAI have limited efficacy and elevated hepatotoxicity, emphasizing the demand for treatment regimens that have better patient outcomes. In this project, we explored a drug repurposing strategy by evaluating FDA-approved chemotherapeutic agents with pharmacokinetic properties compatible with HAI delivery. Drugs were selected using established pharmacokinetic databases and then tested in vitro using CRC cell models and a normal epithelial liver cell line to assess cytotoxicity and dose-response. In addition, we investigated the therapeutic potential of combining a microtubule destabilizer with an FDA-approved fatty acid synthase (FASN) inhibitor. Synergy experiments demonstrated enhanced cytotoxic effects when chemotherapeutics were combined with the FASN inhibitor, suggesting that there is potential for a novel treatment regimen for patients presenting with this disease. These preliminary findings support drug repurposing within the context of HAI delivery as a clinically translatable approach. By utilizing existing FDA-approved compounds of both chemotherapeutic agents and metabolic inhibitors, this strategy may lay the groundwork for novel therapies for patients with CRLM. Further preclinical and translational studies will be necessary to define optimal drug combinations and dosing regimens, with the ultimate goal of expanding therapeutic options and improving outcomes for this high-risk patient population. Citation Format: Manasa Ravi, Colin M. Court, April Risinger. Repurposed FDA-approved agents for hepatic artery infusion in colorectal liver metastases [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 4459.

Cancer ResearchVol. 86(7_Supplement)
The University of Texas at San Antonio Health Science Center (US), The University of Texas Health Science Center at Houston (US)
Good health and well-being
Openalex Percentile: Top 11%
Cancer, Lipids, and Metabolism
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