Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:2195135rdf:typepubmed:Citationlld:pubmed
pubmed-article:2195135lifeskim:mentionsumls-concept:C0030705lld:lifeskim
pubmed-article:2195135lifeskim:mentionsumls-concept:C0009402lld:lifeskim
pubmed-article:2195135lifeskim:mentionsumls-concept:C0008838lld:lifeskim
pubmed-article:2195135lifeskim:mentionsumls-concept:C0016360lld:lifeskim
pubmed-article:2195135lifeskim:mentionsumls-concept:C0023413lld:lifeskim
pubmed-article:2195135lifeskim:mentionsumls-concept:C0600688lld:lifeskim
pubmed-article:2195135lifeskim:mentionsumls-concept:C0205390lld:lifeskim
pubmed-article:2195135lifeskim:mentionsumls-concept:C2603343lld:lifeskim
pubmed-article:2195135lifeskim:mentionsumls-concept:C0205195lld:lifeskim
pubmed-article:2195135lifeskim:mentionsumls-concept:C0205179lld:lifeskim
pubmed-article:2195135lifeskim:mentionsumls-concept:C2348767lld:lifeskim
pubmed-article:2195135pubmed:dateCreated1990-8-15lld:pubmed
pubmed-article:2195135pubmed:abstractText5-Fluorouracil (5-FU) has been the treatment of choice for colorectal carcinoma with an overall response rate of about 20%. Recent studies have shown that folate (LV) can increase 5-FU therapeutic efficacy, achieving about a 40% response rate without a clear impact on survival. Cisplatinum (CDDP) is usually inactive in colorectal carcinoma, but the association with 5-FU results in a synergistic antineoplastic effect. A phase I-II study was done to assess the maximally tolerated dose (MTD) of CDDP in association with 5-FU + LV. The MTD for CDDP was 20 mg/m2/wk in association with 5-FU 400-500 mg/m2/wk and LV 500 mg/m2/wk. WHO criteria were used for evaluation of both toxicity and response. In the phase I part we found that the main side-effect in 27 evaluable patients (pts) was gastrointestinal toxicity, mainly in the form of nausea/vomiting (92%) and diarrhea (70%) which caused one therapy-related death. Renal (26%) and marrow (59%) toxicity were acceptable. In the phase II part of the study 1 out of 19 evaluable pts (5%) had a complete response of 309 days, 3 pts achieved a partial response (16%) with a median duration od 410 days, 2 pts had a minimal response (10%) with a median duration of 261 days, and 8 pts experienced no change (42%) with a mean duration of 196 + days. In our opinion the 21% response rate obtained in this series is not satisfactory. Nevertheless the very high number of minimal response + no change patients together with the interesting impact on survival in responders may suggest further phase II-III studies.lld:pubmed
pubmed-article:2195135pubmed:languageenglld:pubmed
pubmed-article:2195135pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2195135pubmed:citationSubsetIMlld:pubmed
pubmed-article:2195135pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2195135pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2195135pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2195135pubmed:statusMEDLINElld:pubmed
pubmed-article:2195135pubmed:monthFeblld:pubmed
pubmed-article:2195135pubmed:issn1120-009Xlld:pubmed
pubmed-article:2195135pubmed:authorpubmed-author:RussoAAlld:pubmed
pubmed-article:2195135pubmed:authorpubmed-author:RausaLLlld:pubmed
pubmed-article:2195135pubmed:authorpubmed-author:GebbiaNNlld:pubmed
pubmed-article:2195135pubmed:authorpubmed-author:RustumYYlld:pubmed
pubmed-article:2195135pubmed:authorpubmed-author:PalmeriSSlld:pubmed
pubmed-article:2195135pubmed:authorpubmed-author:GebbiaVVlld:pubmed
pubmed-article:2195135pubmed:authorpubmed-author:BorsellinoNNlld:pubmed
pubmed-article:2195135pubmed:issnTypePrintlld:pubmed
pubmed-article:2195135pubmed:volume2 Suppl 1lld:pubmed
pubmed-article:2195135pubmed:ownerNLMlld:pubmed
pubmed-article:2195135pubmed:authorsCompleteYlld:pubmed
pubmed-article:2195135pubmed:pagination28-32lld:pubmed
pubmed-article:2195135pubmed:dateRevised2009-8-4lld:pubmed
pubmed-article:2195135pubmed:meshHeadingpubmed-meshheading:2195135-...lld:pubmed
pubmed-article:2195135pubmed:meshHeadingpubmed-meshheading:2195135-...lld:pubmed
pubmed-article:2195135pubmed:meshHeadingpubmed-meshheading:2195135-...lld:pubmed
pubmed-article:2195135pubmed:meshHeadingpubmed-meshheading:2195135-...lld:pubmed
pubmed-article:2195135pubmed:meshHeadingpubmed-meshheading:2195135-...lld:pubmed
pubmed-article:2195135pubmed:meshHeadingpubmed-meshheading:2195135-...lld:pubmed
pubmed-article:2195135pubmed:meshHeadingpubmed-meshheading:2195135-...lld:pubmed
pubmed-article:2195135pubmed:meshHeadingpubmed-meshheading:2195135-...lld:pubmed
pubmed-article:2195135pubmed:meshHeadingpubmed-meshheading:2195135-...lld:pubmed
pubmed-article:2195135pubmed:meshHeadingpubmed-meshheading:2195135-...lld:pubmed
pubmed-article:2195135pubmed:meshHeadingpubmed-meshheading:2195135-...lld:pubmed
pubmed-article:2195135pubmed:meshHeadingpubmed-meshheading:2195135-...lld:pubmed
pubmed-article:2195135pubmed:meshHeadingpubmed-meshheading:2195135-...lld:pubmed
pubmed-article:2195135pubmed:year1990lld:pubmed
pubmed-article:2195135pubmed:articleTitleA phase I-II study on the toxicity and therapeutic efficacy of 5-fluorouracil in combination with leucovorin and cisplatinum in patients with advanced colorectal carcinoma.lld:pubmed
pubmed-article:2195135pubmed:affiliationIstituto di Farmacologia, Università di Palermo, Italy.lld:pubmed
pubmed-article:2195135pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:2195135pubmed:publicationTypeClinical Triallld:pubmed