Loading…
Hepatic arterial chemotherapy for metastatic colorectal carcinoma
In this review, the rationale of regional chemotherapy for treatment of hepatic metastases in advanced colorectal carcinoma is discussed. Pharmacokinetic principles and early clinical experience of hepatic arterial drug administration are summarised. The regional advantage of fluoropyrimidine compou...
Saved in:
Published in: | British journal of cancer 1994-02, Vol.69 (2), p.372-378 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c429t-ecb1e30a81c0f4d179b60fa2c52e0b7ca34f937137f8cc2c458b475f20304223 |
---|---|
cites | |
container_end_page | 378 |
container_issue | 2 |
container_start_page | 372 |
container_title | British journal of cancer |
container_volume | 69 |
creator | DE TAKATS, P. G KERR, D. J POOLE, C. J WARREN, H. W MCARDLE, C. S |
description | In this review, the rationale of regional chemotherapy for treatment of hepatic metastases in advanced colorectal carcinoma is discussed. Pharmacokinetic principles and early clinical experience of hepatic arterial drug administration are summarised. The regional advantage of fluoropyrimidine compounds in this setting is well established, and recent evidence suggests that 5-fluorouracil (5-FU) is more efficacious than the analogue 5-fluoro-2'-deoxyuridine (FUDR). However, while significantly higher clinical response rates can be achieved with hepatic arterial infusion (HAI) chemotherapy compared with conventional intravenous drug administration, patient survival benefit is not significantly different. Several novel approaches to overcome the limitations of HAI therapy are currently being explored. These include concomitant use of biodegradable microspheres, which both slow tumour blood flow and enhance tumour drug uptake, and use of vasoactive agents to redistribute arterial blood flow towards tumours. In addition, novel chemotherapeutic agents which exploit unique biological characteristics of hepatic tumours are entering clinical trial. |
doi_str_mv | 10.1038/bjc.1994.68 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1968698</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>76348421</sourcerecordid><originalsourceid>FETCH-LOGICAL-c429t-ecb1e30a81c0f4d179b60fa2c52e0b7ca34f937137f8cc2c458b475f20304223</originalsourceid><addsrcrecordid>eNpVkE1r3DAURUVJSKZpV12XziJ0UzzRly1pExhC2wQC2WQvnl-eOg62NZE0hfz72J1haFbicQ_3isPYF8FXgit71T7jSjinV439wBaiVrISVpoTtuCcm4o7yc_Zx5yfp9Nxa87YmZXOGGUXbH1LWygdLiEVSh30S9zQEMuGEmxflyGm5UAFcvkHYexjIiwzBgm7MQ7wiZ0G6DN9PrwX7PHXz8eb2-r-4ffdzfq-Qi1dqQhbQYqDFciDfhLGtQ0PILGWxFuDoHRwyghlgkWUqGvbalMHyRXXUqoLdr2v3e7agZ6QxpKg99vUDZBefYTOv0_GbuP_xL9euMY2zk4F3w8FKb7sKBc_dBmp72GkuMveNEpbLcUE_tiDmGLOicJxRHA_C_eTcD8L981c-_X_fx3Zg-EpvzzkkBH6kGDELh8x5YTktZ6wb3tshLJLdMynqXlpGnoDqCWU4g</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>76348421</pqid></control><display><type>article</type><title>Hepatic arterial chemotherapy for metastatic colorectal carcinoma</title><source>PubMed Central</source><creator>DE TAKATS, P. G ; KERR, D. J ; POOLE, C. J ; WARREN, H. W ; MCARDLE, C. S</creator><creatorcontrib>DE TAKATS, P. G ; KERR, D. J ; POOLE, C. J ; WARREN, H. W ; MCARDLE, C. S</creatorcontrib><description>In this review, the rationale of regional chemotherapy for treatment of hepatic metastases in advanced colorectal carcinoma is discussed. Pharmacokinetic principles and early clinical experience of hepatic arterial drug administration are summarised. The regional advantage of fluoropyrimidine compounds in this setting is well established, and recent evidence suggests that 5-fluorouracil (5-FU) is more efficacious than the analogue 5-fluoro-2'-deoxyuridine (FUDR). However, while significantly higher clinical response rates can be achieved with hepatic arterial infusion (HAI) chemotherapy compared with conventional intravenous drug administration, patient survival benefit is not significantly different. Several novel approaches to overcome the limitations of HAI therapy are currently being explored. These include concomitant use of biodegradable microspheres, which both slow tumour blood flow and enhance tumour drug uptake, and use of vasoactive agents to redistribute arterial blood flow towards tumours. In addition, novel chemotherapeutic agents which exploit unique biological characteristics of hepatic tumours are entering clinical trial.</description><identifier>ISSN: 0007-0920</identifier><identifier>EISSN: 1532-1827</identifier><identifier>DOI: 10.1038/bjc.1994.68</identifier><identifier>PMID: 8297738</identifier><identifier>CODEN: BJCAAI</identifier><language>eng</language><publisher>Basingstoke: Nature Publishing Group</publisher><subject><![CDATA[Antineoplastic agents ; Biological and medical sciences ; Chemotherapy ; Colorectal Neoplasms ; Floxuridine - administration & dosage ; Fluorouracil - administration & dosage ; Hepatic Artery ; Humans ; Infusions, Intra-Arterial ; Liver Neoplasms - drug therapy ; Liver Neoplasms - secondary ; Maleic Anhydrides - administration & dosage ; Medical sciences ; Mitomycin - administration & dosage ; Pharmacology. Drug treatments ; Polystyrenes - administration & dosage ; Zinostatin - administration & dosage ; Zinostatin - analogs & derivatives]]></subject><ispartof>British journal of cancer, 1994-02, Vol.69 (2), p.372-378</ispartof><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c429t-ecb1e30a81c0f4d179b60fa2c52e0b7ca34f937137f8cc2c458b475f20304223</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968698/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968698/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3912054$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8297738$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>DE TAKATS, P. G</creatorcontrib><creatorcontrib>KERR, D. J</creatorcontrib><creatorcontrib>POOLE, C. J</creatorcontrib><creatorcontrib>WARREN, H. W</creatorcontrib><creatorcontrib>MCARDLE, C. S</creatorcontrib><title>Hepatic arterial chemotherapy for metastatic colorectal carcinoma</title><title>British journal of cancer</title><addtitle>Br J Cancer</addtitle><description>In this review, the rationale of regional chemotherapy for treatment of hepatic metastases in advanced colorectal carcinoma is discussed. Pharmacokinetic principles and early clinical experience of hepatic arterial drug administration are summarised. The regional advantage of fluoropyrimidine compounds in this setting is well established, and recent evidence suggests that 5-fluorouracil (5-FU) is more efficacious than the analogue 5-fluoro-2'-deoxyuridine (FUDR). However, while significantly higher clinical response rates can be achieved with hepatic arterial infusion (HAI) chemotherapy compared with conventional intravenous drug administration, patient survival benefit is not significantly different. Several novel approaches to overcome the limitations of HAI therapy are currently being explored. These include concomitant use of biodegradable microspheres, which both slow tumour blood flow and enhance tumour drug uptake, and use of vasoactive agents to redistribute arterial blood flow towards tumours. In addition, novel chemotherapeutic agents which exploit unique biological characteristics of hepatic tumours are entering clinical trial.</description><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Chemotherapy</subject><subject>Colorectal Neoplasms</subject><subject>Floxuridine - administration & dosage</subject><subject>Fluorouracil - administration & dosage</subject><subject>Hepatic Artery</subject><subject>Humans</subject><subject>Infusions, Intra-Arterial</subject><subject>Liver Neoplasms - drug therapy</subject><subject>Liver Neoplasms - secondary</subject><subject>Maleic Anhydrides - administration & dosage</subject><subject>Medical sciences</subject><subject>Mitomycin - administration & dosage</subject><subject>Pharmacology. Drug treatments</subject><subject>Polystyrenes - administration & dosage</subject><subject>Zinostatin - administration & dosage</subject><subject>Zinostatin - analogs & derivatives</subject><issn>0007-0920</issn><issn>1532-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><recordid>eNpVkE1r3DAURUVJSKZpV12XziJ0UzzRly1pExhC2wQC2WQvnl-eOg62NZE0hfz72J1haFbicQ_3isPYF8FXgit71T7jSjinV439wBaiVrISVpoTtuCcm4o7yc_Zx5yfp9Nxa87YmZXOGGUXbH1LWygdLiEVSh30S9zQEMuGEmxflyGm5UAFcvkHYexjIiwzBgm7MQ7wiZ0G6DN9PrwX7PHXz8eb2-r-4ffdzfq-Qi1dqQhbQYqDFciDfhLGtQ0PILGWxFuDoHRwyghlgkWUqGvbalMHyRXXUqoLdr2v3e7agZ6QxpKg99vUDZBefYTOv0_GbuP_xL9euMY2zk4F3w8FKb7sKBc_dBmp72GkuMveNEpbLcUE_tiDmGLOicJxRHA_C_eTcD8L981c-_X_fx3Zg-EpvzzkkBH6kGDELh8x5YTktZ6wb3tshLJLdMynqXlpGnoDqCWU4g</recordid><startdate>19940201</startdate><enddate>19940201</enddate><creator>DE TAKATS, P. G</creator><creator>KERR, D. J</creator><creator>POOLE, C. J</creator><creator>WARREN, H. W</creator><creator>MCARDLE, C. S</creator><general>Nature Publishing Group</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19940201</creationdate><title>Hepatic arterial chemotherapy for metastatic colorectal carcinoma</title><author>DE TAKATS, P. G ; KERR, D. J ; POOLE, C. J ; WARREN, H. W ; MCARDLE, C. S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c429t-ecb1e30a81c0f4d179b60fa2c52e0b7ca34f937137f8cc2c458b475f20304223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Antineoplastic agents</topic><topic>Biological and medical sciences</topic><topic>Chemotherapy</topic><topic>Colorectal Neoplasms</topic><topic>Floxuridine - administration & dosage</topic><topic>Fluorouracil - administration & dosage</topic><topic>Hepatic Artery</topic><topic>Humans</topic><topic>Infusions, Intra-Arterial</topic><topic>Liver Neoplasms - drug therapy</topic><topic>Liver Neoplasms - secondary</topic><topic>Maleic Anhydrides - administration & dosage</topic><topic>Medical sciences</topic><topic>Mitomycin - administration & dosage</topic><topic>Pharmacology. Drug treatments</topic><topic>Polystyrenes - administration & dosage</topic><topic>Zinostatin - administration & dosage</topic><topic>Zinostatin - analogs & derivatives</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>DE TAKATS, P. G</creatorcontrib><creatorcontrib>KERR, D. J</creatorcontrib><creatorcontrib>POOLE, C. J</creatorcontrib><creatorcontrib>WARREN, H. W</creatorcontrib><creatorcontrib>MCARDLE, C. S</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>DE TAKATS, P. G</au><au>KERR, D. J</au><au>POOLE, C. J</au><au>WARREN, H. W</au><au>MCARDLE, C. S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hepatic arterial chemotherapy for metastatic colorectal carcinoma</atitle><jtitle>British journal of cancer</jtitle><addtitle>Br J Cancer</addtitle><date>1994-02-01</date><risdate>1994</risdate><volume>69</volume><issue>2</issue><spage>372</spage><epage>378</epage><pages>372-378</pages><issn>0007-0920</issn><eissn>1532-1827</eissn><coden>BJCAAI</coden><abstract>In this review, the rationale of regional chemotherapy for treatment of hepatic metastases in advanced colorectal carcinoma is discussed. Pharmacokinetic principles and early clinical experience of hepatic arterial drug administration are summarised. The regional advantage of fluoropyrimidine compounds in this setting is well established, and recent evidence suggests that 5-fluorouracil (5-FU) is more efficacious than the analogue 5-fluoro-2'-deoxyuridine (FUDR). However, while significantly higher clinical response rates can be achieved with hepatic arterial infusion (HAI) chemotherapy compared with conventional intravenous drug administration, patient survival benefit is not significantly different. Several novel approaches to overcome the limitations of HAI therapy are currently being explored. These include concomitant use of biodegradable microspheres, which both slow tumour blood flow and enhance tumour drug uptake, and use of vasoactive agents to redistribute arterial blood flow towards tumours. In addition, novel chemotherapeutic agents which exploit unique biological characteristics of hepatic tumours are entering clinical trial.</abstract><cop>Basingstoke</cop><pub>Nature Publishing Group</pub><pmid>8297738</pmid><doi>10.1038/bjc.1994.68</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0007-0920 |
ispartof | British journal of cancer, 1994-02, Vol.69 (2), p.372-378 |
issn | 0007-0920 1532-1827 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1968698 |
source | PubMed Central |
subjects | Antineoplastic agents Biological and medical sciences Chemotherapy Colorectal Neoplasms Floxuridine - administration & dosage Fluorouracil - administration & dosage Hepatic Artery Humans Infusions, Intra-Arterial Liver Neoplasms - drug therapy Liver Neoplasms - secondary Maleic Anhydrides - administration & dosage Medical sciences Mitomycin - administration & dosage Pharmacology. Drug treatments Polystyrenes - administration & dosage Zinostatin - administration & dosage Zinostatin - analogs & derivatives |
title | Hepatic arterial chemotherapy for metastatic colorectal carcinoma |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T00%3A35%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Hepatic%20arterial%20chemotherapy%20for%20metastatic%20colorectal%20carcinoma&rft.jtitle=British%20journal%20of%20cancer&rft.au=DE%20TAKATS,%20P.%20G&rft.date=1994-02-01&rft.volume=69&rft.issue=2&rft.spage=372&rft.epage=378&rft.pages=372-378&rft.issn=0007-0920&rft.eissn=1532-1827&rft.coden=BJCAAI&rft_id=info:doi/10.1038/bjc.1994.68&rft_dat=%3Cproquest_pubme%3E76348421%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c429t-ecb1e30a81c0f4d179b60fa2c52e0b7ca34f937137f8cc2c458b475f20304223%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=76348421&rft_id=info:pmid/8297738&rfr_iscdi=true |