Dose Versus pharmacokinetics for predicting tolerance to 5‐day continuous infusion of 5‐FU
This non‐randomized study reports pharmaco‐clinical data on 5‐FU administered by the widely used 5‐day continuous infusion schedule to 42 patients with metastatic colorectal cancer; 5‐FU was given by hepatic intra‐arterial route (h.i.a.) at doses ranging from 800 to 1,450 mg/m2, and by a systemic in...
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Veröffentlicht in: | International journal of cancer 1988-04, Vol.41 (4), p.537-541 |
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container_title | International journal of cancer |
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creator | Milano, G. Roman, P. Khater, R. Frenay, M. Renee, N. Namer, M. |
description | This non‐randomized study reports pharmaco‐clinical data on 5‐FU administered by the widely used 5‐day continuous infusion schedule to 42 patients with metastatic colorectal cancer; 5‐FU was given by hepatic intra‐arterial route (h.i.a.) at doses ranging from 800 to 1,450 mg/m2, and by a systemic intravenous route (i.v.) at doses ranging from 650 to 1,300 mg/m2. 5‐FU blood levels were available for a total of 179 cycles. Toxicity was dose‐de pendent during h.i.a. cycles but not during i.v. cycles. For h.i.a. cycles, 1,000 mg/m2/day represented the threshold dose for tolerance. The individual total cycle drug concentration‐time product might predict toxicity for both i.v. and h.i.a. cycle when the threshold is set at 30,000 ng/ml hr. These data may be of practical value for improving the therapeutic index of 5‐day continuous treatment by 5‐FU given by i.v. or h.i.a. routes. |
doi_str_mv | 10.1002/ijc.2910410411 |
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Toxicity was dose‐de pendent during h.i.a. cycles but not during i.v. cycles. For h.i.a. cycles, 1,000 mg/m2/day represented the threshold dose for tolerance. The individual total cycle drug concentration‐time product might predict toxicity for both i.v. and h.i.a. cycle when the threshold is set at 30,000 ng/ml hr. These data may be of practical value for improving the therapeutic index of 5‐day continuous treatment by 5‐FU given by i.v. or h.i.a. routes.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.2910410411</identifier><identifier>PMID: 3356488</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Aged ; Antineoplastic agents ; Biological and medical sciences ; Chemotherapy ; Dose-Response Relationship, Drug ; Female ; Fluorouracil - administration & dosage ; Fluorouracil - adverse effects ; Fluorouracil - pharmacokinetics ; Hepatic Artery ; Humans ; Infusions, Intra-Arterial ; Infusions, Intravenous ; Male ; Medical sciences ; Middle Aged ; Pharmacology. Drug treatments</subject><ispartof>International journal of cancer, 1988-04, Vol.41 (4), p.537-541</ispartof><rights>Copyright © 1988 Wiley‐Liss, Inc., A Wiley Company</rights><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4951-53dc2b05edc36def5bc2bad5bd24f7032cfb5029fe002dabf88d3cb26bc2e8673</citedby><cites>FETCH-LOGICAL-c4951-53dc2b05edc36def5bc2bad5bd24f7032cfb5029fe002dabf88d3cb26bc2e8673</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fijc.2910410411$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.2910410411$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7019316$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3356488$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Milano, G.</creatorcontrib><creatorcontrib>Roman, P.</creatorcontrib><creatorcontrib>Khater, R.</creatorcontrib><creatorcontrib>Frenay, M.</creatorcontrib><creatorcontrib>Renee, N.</creatorcontrib><creatorcontrib>Namer, M.</creatorcontrib><title>Dose Versus pharmacokinetics for predicting tolerance to 5‐day continuous infusion of 5‐FU</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>This non‐randomized study reports pharmaco‐clinical data on 5‐FU administered by the widely used 5‐day continuous infusion schedule to 42 patients with metastatic colorectal cancer; 5‐FU was given by hepatic intra‐arterial route (h.i.a.) at doses ranging from 800 to 1,450 mg/m2, and by a systemic intravenous route (i.v.) at doses ranging from 650 to 1,300 mg/m2. 5‐FU blood levels were available for a total of 179 cycles. Toxicity was dose‐de pendent during h.i.a. cycles but not during i.v. cycles. For h.i.a. cycles, 1,000 mg/m2/day represented the threshold dose for tolerance. The individual total cycle drug concentration‐time product might predict toxicity for both i.v. and h.i.a. cycle when the threshold is set at 30,000 ng/ml hr. These data may be of practical value for improving the therapeutic index of 5‐day continuous treatment by 5‐FU given by i.v. or h.i.a. routes.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Chemotherapy</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Fluorouracil - administration & dosage</subject><subject>Fluorouracil - adverse effects</subject><subject>Fluorouracil - pharmacokinetics</subject><subject>Hepatic Artery</subject><subject>Humans</subject><subject>Infusions, Intra-Arterial</subject><subject>Infusions, Intravenous</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkLtOwzAUhi0EKqWwsiFlQGwpdhznMqJCoQiJhTISOfYxuCRxsROhbjwCz8iT4NKosCEdycf6v3P7ETomeEwwjs71QoyjnOB4HWQHDQnO0xBHhO2ioQdwmBKa7KMD5xYYE8JwPEADSlkSZ9kQPV0aB8EjWNe5YPnCbc2FedUNtFq4QBkbLC1ILVrdPAetqcDyRoDPAvb18Sn5KhCm8WJnfL1uVOe0aQKjfuTp_BDtKV45OOrfEZpPrx4mN-Hd_fVscnEXijhnJGRUiqjEDKSgiQTFSv_lkpUyilWKaSRUyXCUK_AXSV6qLJNUlFHiOciSlI7Q2abv0pq3Dlxb1NoJqCregN-s8GczSljswfEGFNY4Z0EVS6trblcFwcXa0MIbWvwa6gtO-s5dWYPc4r2DXj_tde4Er9TaH-22WIpJTknisXyDvesKVv8MLWa3kz8rfAOaHpGU</recordid><startdate>19880415</startdate><enddate>19880415</enddate><creator>Milano, G.</creator><creator>Roman, P.</creator><creator>Khater, R.</creator><creator>Frenay, M.</creator><creator>Renee, N.</creator><creator>Namer, M.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</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>7U7</scope><scope>C1K</scope></search><sort><creationdate>19880415</creationdate><title>Dose Versus pharmacokinetics for predicting tolerance to 5‐day continuous infusion of 5‐FU</title><author>Milano, G. ; Roman, P. ; Khater, R. ; Frenay, M. ; Renee, N. ; Namer, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4951-53dc2b05edc36def5bc2bad5bd24f7032cfb5029fe002dabf88d3cb26bc2e8673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic agents</topic><topic>Biological and medical sciences</topic><topic>Chemotherapy</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Fluorouracil - administration & dosage</topic><topic>Fluorouracil - adverse effects</topic><topic>Fluorouracil - pharmacokinetics</topic><topic>Hepatic Artery</topic><topic>Humans</topic><topic>Infusions, Intra-Arterial</topic><topic>Infusions, Intravenous</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pharmacology. Drug treatments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Milano, G.</creatorcontrib><creatorcontrib>Roman, P.</creatorcontrib><creatorcontrib>Khater, R.</creatorcontrib><creatorcontrib>Frenay, M.</creatorcontrib><creatorcontrib>Renee, N.</creatorcontrib><creatorcontrib>Namer, M.</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>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Milano, G.</au><au>Roman, P.</au><au>Khater, R.</au><au>Frenay, M.</au><au>Renee, N.</au><au>Namer, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dose Versus pharmacokinetics for predicting tolerance to 5‐day continuous infusion of 5‐FU</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>1988-04-15</date><risdate>1988</risdate><volume>41</volume><issue>4</issue><spage>537</spage><epage>541</epage><pages>537-541</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>This non‐randomized study reports pharmaco‐clinical data on 5‐FU administered by the widely used 5‐day continuous infusion schedule to 42 patients with metastatic colorectal cancer; 5‐FU was given by hepatic intra‐arterial route (h.i.a.) at doses ranging from 800 to 1,450 mg/m2, and by a systemic intravenous route (i.v.) at doses ranging from 650 to 1,300 mg/m2. 5‐FU blood levels were available for a total of 179 cycles. Toxicity was dose‐de pendent during h.i.a. cycles but not during i.v. cycles. For h.i.a. cycles, 1,000 mg/m2/day represented the threshold dose for tolerance. The individual total cycle drug concentration‐time product might predict toxicity for both i.v. and h.i.a. cycle when the threshold is set at 30,000 ng/ml hr. These data may be of practical value for improving the therapeutic index of 5‐day continuous treatment by 5‐FU given by i.v. or h.i.a. routes.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>3356488</pmid><doi>10.1002/ijc.2910410411</doi><tpages>5</tpages></addata></record> |
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subjects | Adult Aged Antineoplastic agents Biological and medical sciences Chemotherapy Dose-Response Relationship, Drug Female Fluorouracil - administration & dosage Fluorouracil - adverse effects Fluorouracil - pharmacokinetics Hepatic Artery Humans Infusions, Intra-Arterial Infusions, Intravenous Male Medical sciences Middle Aged Pharmacology. Drug treatments |
title | Dose Versus pharmacokinetics for predicting tolerance to 5‐day continuous infusion of 5‐FU |
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