Toward a Better Understanding of The Mechanism Of Action for Intra-Arterial Delivery of Irinotecan From Dc Bead (TM) (DEBIRI)
Author(s) -
Andrew L. Lewis,
Brenda Hall
Publication year - 2019
Publication title -
future oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.857
H-Index - 72
eISSN - 1744-8301
pISSN - 1479-6694
DOI - 10.2217/fon-2019-0071
Subject(s) - medicine , irinotecan , mechanism (biology) , mechanism of action , action (physics) , bead , pharmacology , cancer , epistemology , biochemistry , chemistry , composite material , quantum mechanics , in vitro , philosophy , materials science , colorectal cancer , physics
DC Bead is designed for the embolization of liver malignancies combined with local sustained chemotherapy delivery. It was first demonstrated around a decade ago that irinotecan could be loaded into DC Bead and used in a transarterially directed procedure to treat colorectal liver metastases, commonly referred to as drug-eluting bead with irinotecan (DEBIRI). Despite numerous reports of its safe and effective use in treating colorectal liver metastases patients, there remains a perceived fundamental paradox as to how this treatment works. This review of the mechanism of action of DEBIRI provides a rationale for why intra-arterial delivery of this prodrug from an embolic bead provides for enhanced tumor selectivity, sparing the normal liver while reducing adverse side effects associated with the irinotecan therapy. [Formula: see text]
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