Literature DB >> 32300759

Endovascular Ion Exchange Chemofiltration Device Reduces Off-Target Doxorubicin Exposure in a Hepatic Intra-arterial Chemotherapy Model.

Colin Yee1,2, David McCoy1,2, Jay Yu1,2, Aaron Losey1,2, Caroline Jordan1,2, Terilyn Moore1,2, Carol Stillson1,2, Hee Jeung Oh1,2, Bridget Kilbride1,2, Shuvo Roy1,2, Anand Patel1,2, Mark W Wilson1,2, Steven W Hetts1,2.   

Abstract

Purpose: To determine if endovascular chemofiltration with an ionic device (ChemoFilter [CF]) can be used to reduce systemic exposure and off-target biodistribution of doxorubicin (DOX) during hepatic intra-arterial chemotherapy (IAC) in a preclinical model. Materials and
Methods: Hepatic IAC infusions were performed in six pigs with normal livers. Animals underwent two 10-minute intra-arterial infusions of DOX (200 mg) into the common hepatic artery. Both the treatment group and the control group received initial IAC at 0 minutes and a second dose at 200 minutes. Prior to the second dose, CF devices were deployed in and adjacent to the hepatic venous outflow tract of treatment animals. Systemic exposure to DOX was monitored via blood samples taken during IAC procedures. After euthanasia, organ tissue DOX concentrations were analyzed. Alterations in systemic DOX exposure and biodistribution were compared by using one-tailed t tests.
Results: CF devices were well tolerated, and no hemodynamic, thrombotic, or immunologic complications were observed. Animals treated with a CF device had a significant reduction in systemic exposure when compared with systemic exposure in the control group (P <.009). Treatment with a CF device caused a significant decrease in peak DOX concentration (31%, P <.01) and increased the time to maximum concentration (P <.03). Tissue analysis was used to confirm significant reduction in DOX accumulation in the heart and kidneys (P <.001 and P <.022, respectively). Mean tissue concentrations in the heart, kidneys, and liver of animals treated with CF compared with those in control animals were 14.2 μg/g ± 1.9 (standard deviation) versus 26.0 μg/g ± 1.8, 46.4 μg/g ± 4.6 versus 172.6 μg/g ± 40.2, and 217.0 μg/g ± 5.1 versus 236.8 μg/g ± 9.0, respectively. Fluorescence imaging was used to confirm in vivo DOX binding to CF devices.
Conclusion: Reduced systemic exposure and heart bioaccumulation of DOX during local-regional chemotherapy to the liver can be achieved through in situ adsorption by minimally invasive image-guided CF devices.© RSNA, 2019. 2019 by the Radiological Society of North America, Inc.

Entities:  

Year:  2019        PMID: 32300759      PMCID: PMC7134535          DOI: 10.1148/rycan.2019190009

Source DB:  PubMed          Journal:  Radiol Imaging Cancer        ISSN: 2638-616X


  38 in total

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Review 4.  Locoregional and systemic therapy for hepatocellular carcinoma.

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Review 5.  Current status of isolated hepatic perfusion with or without tumor necrosis factor for the treatment of unresectable cancers confined to liver.

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Authors:  Andrea M Abbott; Matthew P Doepker; Youngchul Kim; Matthew C Perez; Cassandra Gandle; Kerry L Thomas; Junsung Choi; Ravi Shridhar; Jonathan S Zager
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Review 7.  Chemosaturation With Percutaneous Hepatic Perfusion in Unresectable Hepatic Metastases.

Authors:  Evan S Glazer; Jonathan S Zager
Journal:  Cancer Control       Date:  2017-01       Impact factor: 3.302

Review 8.  Hepatocellular carcinoma locoregional therapies for patients in the waiting list. Impact on transplantability and recurrence rate.

Authors:  Matteo Cescon; Alessandro Cucchetti; Matteo Ravaioli; Antonio Daniele Pinna
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Review 9.  Doxorubicin: the good, the bad and the ugly effect.

Authors:  Cristina Carvalho; Renato X Santos; Susana Cardoso; Sónia Correia; Paulo J Oliveira; Maria S Santos; Paula I Moreira
Journal:  Curr Med Chem       Date:  2009-09-01       Impact factor: 4.530

10.  Randomized Trial of Hepatic Artery Embolization for Hepatocellular Carcinoma Using Doxorubicin-Eluting Microspheres Compared With Embolization With Microspheres Alone.

Authors:  Karen T Brown; Richard K Do; Mithat Gonen; Anne M Covey; George I Getrajdman; Constantinos T Sofocleous; William R Jarnagin; Michael I D'Angelica; Peter J Allen; Joseph P Erinjeri; Lynn A Brody; Gerald P O'Neill; Kristian N Johnson; Alessandra R Garcia; Christopher Beattie; Binsheng Zhao; Stephen B Solomon; Lawrence H Schwartz; Ronald DeMatteo; Ghassan K Abou-Alfa
Journal:  J Clin Oncol       Date:  2016-02-01       Impact factor: 44.544

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  3 in total

1.  Engineering hairy cellulose nanocrystals for chemotherapy drug capture.

Authors:  Sarah A E Young; Joy Muthami; Mica Pitcher; Petar Antovski; Patricia Wamea; Robert Denis Murphy; Reihaneh Haghniaz; Andrew Schmidt; Samuel Clark; Ali Khademhosseini; Amir Sheikhi
Journal:  Mater Today Chem       Date:  2021-12-30

2.  Evaluating Radioactive Analogs of Doxorubicin to Quantify ChemoFilter Binding and Whole-Body Positron Emission Tomography/Magnetic Resonance Imaging for Drug Biodistribution.

Authors:  Parth Kumar; Colin Yee; Joseph E Blecha; Thomas R Hayes; Bridget F Kilbride; Carol Stillson; Aaron D Losey; Eric Mastria; Caroline D Jordan; Tony L Huynh; Terilyn Moore; Mark W Wilson; Henry F VanBrocklin; Steven W Hetts
Journal:  J Vasc Interv Radiol       Date:  2022-03-15       Impact factor: 3.682

3.  Progress in Natural Compounds/siRNA Co-delivery Employing Nanovehicles for Cancer Therapy.

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Journal:  ACS Comb Sci       Date:  2020-10-23       Impact factor: 3.784

  3 in total

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