2001
DOI: 10.1016/s1470-2045(00)00419-8
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Hepatic-arterial chemotherapy

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Cited by 63 publications
(30 citation statements)
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“…This result might is not unexpected considering that trans-arterial treatment is generally accepted as a more effective approach than systemic treatments in liver tumors (24). In a biodistribution study employing intravenous administration of As 2 O 3 , the tissue concentration of monomethylarsinic acid, a major metabolite of As 2 O 3 , was highest in the lung and kidney, suggesting most of systemically administered As 2 O 3 is metabolized in organs other than the liver (25).…”
Section: Discussionmentioning
confidence: 80%
“…This result might is not unexpected considering that trans-arterial treatment is generally accepted as a more effective approach than systemic treatments in liver tumors (24). In a biodistribution study employing intravenous administration of As 2 O 3 , the tissue concentration of monomethylarsinic acid, a major metabolite of As 2 O 3 , was highest in the lung and kidney, suggesting most of systemically administered As 2 O 3 is metabolized in organs other than the liver (25).…”
Section: Discussionmentioning
confidence: 80%
“…Increased response rates can be achieved by increasing the drug delivery to tumors [25]. Intraarterial chemotherapy is successfully used in cancer treatment [15,16] reaching a high first-pass extraction of the drug to the tumor. Therefore, intraarterial chemotherapy has a relative theoretical advantage over systemic chemotherapy, as high local drug concentrations with reduced toxicity can be achieved [26].…”
Section: Discussionmentioning
confidence: 99%
“…Intraarterial chemotherapy has been successfully used in cancer treatment [15,16] reaching a high first-pass extraction of the drug to the tumor. The method has been used in gastric cancer in a few trials [17,18] in an adjuvant setting to prevent the development of liver metastases [19] or in a neoadjuvant setting with encouraging results [20].…”
Section: Introductionmentioning
confidence: 99%
“…1 Nicum et al, 2000). In particular, a derivative, 5-Fluoro-2 deoxyuridine (FUDR), is often continuously administered via a hepatic arterial pump or infusion (Kemeny et al, 1999;Kemeny and Fata, 2001;Tebbutt et al, 2002) and predominantly absorbed by the liver (Ensminger et al, 1978). The dose limiting toxicity for this intervention is hepatobiliary, with reports of inflammation surrounding the biliary tree together with fibrosis of the bile ducts and secondary chemical hepatitis (Cohen and Kemeny, 2003;Skitzki and Chang, 2002), indicating that the biliary duct epithelia are the most susceptible tissues.…”
Section: Introductionmentioning
confidence: 99%