pubmed-article:2804987 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:2804987 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
pubmed-article:2804987 | lifeskim:mentions | umls-concept:C0006826 | lld:lifeskim |
pubmed-article:2804987 | lifeskim:mentions | umls-concept:C0019145 | lld:lifeskim |
pubmed-article:2804987 | lifeskim:mentions | umls-concept:C0205054 | lld:lifeskim |
pubmed-article:2804987 | lifeskim:mentions | umls-concept:C0016360 | lld:lifeskim |
pubmed-article:2804987 | lifeskim:mentions | umls-concept:C0020811 | lld:lifeskim |
pubmed-article:2804987 | lifeskim:mentions | umls-concept:C1521750 | lld:lifeskim |
pubmed-article:2804987 | lifeskim:mentions | umls-concept:C0598717 | lld:lifeskim |
pubmed-article:2804987 | lifeskim:mentions | umls-concept:C0920321 | lld:lifeskim |
pubmed-article:2804987 | lifeskim:mentions | umls-concept:C0205179 | lld:lifeskim |
pubmed-article:2804987 | lifeskim:mentions | umls-concept:C1705938 | lld:lifeskim |
pubmed-article:2804987 | lifeskim:mentions | umls-concept:C1527178 | lld:lifeskim |
pubmed-article:2804987 | pubmed:issue | 22 | lld:pubmed |
pubmed-article:2804987 | pubmed:dateCreated | 1989-12-11 | lld:pubmed |
pubmed-article:2804987 | pubmed:abstractText | Eighteen patients with hepatic metastases primarily from colorectal carcinoma were treated on a phase I protocol employing hepatic artery infusion (HAI) of 5-fluorouracil (FUra) and 5-iodo-2'-deoxyuridine (IdUrd) via implantable infusion pump. Patients received a 14-day continuous HAI of 300 mg/day FUra. During days 8-14 of therapy, patients received IdUrd as a separate 3-h HAI daily x 7. Treatment cycles were repeated every 28 days. IdUrd was escalated from 0.1 to 2.86 mg/kg/day x 7. Myelosuppression and stomatitis were mild and not dose limiting. Hepatotoxicity was dose limiting and similar to that reported for 5-fluoro-2'deoxyuridine alone administered as a 14-day infusion every month. One patient developed a clinical picture consistent with sclerosing cholangitis and another had biopsy-proven cholestasis and triaditis. Catheter complications occurred in 7 of 18 patients. Plasma concentrations of FUra during the 7-day continuous HAI of FUra alone were consistently either undetectable or very low (less than or equal to 0.1 microM). At level 3 (1.0 mg/kg/day IdUrd) and beyond, measurable plasma concentrations of FUra, iodouracil, and IdUrd were found at the end of the daily 3-h infusion of IdUrd. The maximum tolerated dose of IdUrd as administered in this trial is 2.2 mg/kg/day x 7 and the recommended starting dose for further clinical investigation is 1.7 mg/kg/day x 7. | lld:pubmed |
pubmed-article:2804987 | pubmed:language | eng | lld:pubmed |
pubmed-article:2804987 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2804987 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:2804987 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2804987 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2804987 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:2804987 | pubmed:month | Nov | lld:pubmed |
pubmed-article:2804987 | pubmed:issn | 0008-5472 | lld:pubmed |
pubmed-article:2804987 | pubmed:author | pubmed-author:WirtanenG WGW | lld:pubmed |
pubmed-article:2804987 | pubmed:author | pubmed-author:RamirezGG | lld:pubmed |
pubmed-article:2804987 | pubmed:author | pubmed-author:WeeseJ LJL | lld:pubmed |
pubmed-article:2804987 | pubmed:author | pubmed-author:WillsonJ KJK | lld:pubmed |
pubmed-article:2804987 | pubmed:author | pubmed-author:FischerP HPH | lld:pubmed |
pubmed-article:2804987 | pubmed:author | pubmed-author:RemickS CSC | lld:pubmed |
pubmed-article:2804987 | pubmed:author | pubmed-author:BensonA... | lld:pubmed |
pubmed-article:2804987 | pubmed:author | pubmed-author:TutschK DKD | lld:pubmed |
pubmed-article:2804987 | pubmed:author | pubmed-author:AlbertiD BDB | lld:pubmed |
pubmed-article:2804987 | pubmed:author | pubmed-author:NietingL MLM | lld:pubmed |
pubmed-article:2804987 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:2804987 | pubmed:day | 15 | lld:pubmed |
pubmed-article:2804987 | pubmed:volume | 49 | lld:pubmed |
pubmed-article:2804987 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:2804987 | pubmed:authorsComplete | N | lld:pubmed |
pubmed-article:2804987 | pubmed:pagination | 6437-42 | lld:pubmed |
pubmed-article:2804987 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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pubmed-article:2804987 | pubmed:year | 1989 | lld:pubmed |
pubmed-article:2804987 | pubmed:articleTitle | Phase I trial of hepatic artery infusion of 5-iodo-2'-deoxyuridine and 5-fluorouracil in patients with advanced hepatic malignancy: biochemically based combination chemotherapy. | lld:pubmed |
pubmed-article:2804987 | pubmed:affiliation | University of Wisconsin Clinical Cancer Center, Madison. | lld:pubmed |
pubmed-article:2804987 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:2804987 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |