pubmed-article:10839289 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:10839289 | lifeskim:mentions | umls-concept:C0346647 | lld:lifeskim |
pubmed-article:10839289 | lifeskim:mentions | umls-concept:C0016360 | lld:lifeskim |
pubmed-article:10839289 | lifeskim:mentions | umls-concept:C0231220 | lld:lifeskim |
pubmed-article:10839289 | lifeskim:mentions | umls-concept:C0045093 | lld:lifeskim |
pubmed-article:10839289 | lifeskim:mentions | umls-concept:C0282460 | lld:lifeskim |
pubmed-article:10839289 | lifeskim:mentions | umls-concept:C0444889 | lld:lifeskim |
pubmed-article:10839289 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
pubmed-article:10839289 | lifeskim:mentions | umls-concept:C0205195 | lld:lifeskim |
pubmed-article:10839289 | lifeskim:mentions | umls-concept:C0205179 | lld:lifeskim |
pubmed-article:10839289 | pubmed:issue | 11 | lld:pubmed |
pubmed-article:10839289 | pubmed:dateCreated | 2000-6-13 | lld:pubmed |
pubmed-article:10839289 | pubmed:abstractText | Gemcitabine and 5-fluorouracil are the only two compounds with reproducible activity against advanced pancreatic cancer (APC). We have evaluated a novel combination of gemcitabine and 5-fluorouracil on the clinical benefit response (CBR) end point. Eleven consecutive patients with symptomatic APC were entered in a two-stage phase II trial. Gemcitabine was administered by intravenous (i.v.) bolus injection at the dose of 1,000 mg m(-2) on days 1, 8, 15 and 5-fluorouracil 500 mg m(-2) was given by continuous i.v. infusion on days 1-5. Treatment was repeated every 28 days. A CBR was achieved in 7/11 patients. The mean time to loss of CBR was 26.5 weeks (range 14-18, median 22). Toxicity was mild and no APC patient experienced WHO grade 3 toxicity. The gemcitabine/5-fluorouracil combination is well tolerated and produces a symptomatic relief in the majority of APC patients. | lld:pubmed |
pubmed-article:10839289 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10839289 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10839289 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10839289 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10839289 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10839289 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10839289 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10839289 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10839289 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10839289 | pubmed:language | eng | lld:pubmed |
pubmed-article:10839289 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10839289 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:10839289 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10839289 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10839289 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10839289 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:10839289 | pubmed:month | Jun | lld:pubmed |
pubmed-article:10839289 | pubmed:issn | 0007-0920 | lld:pubmed |
pubmed-article:10839289 | pubmed:author | pubmed-author:LibroiaAA | lld:pubmed |
pubmed-article:10839289 | pubmed:author | pubmed-author:BiancoA RAR | lld:pubmed |
pubmed-article:10839289 | pubmed:author | pubmed-author:DamianoVV | lld:pubmed |
pubmed-article:10839289 | pubmed:author | pubmed-author:TagliaferroVV | lld:pubmed |
pubmed-article:10839289 | pubmed:author | pubmed-author:MatanoEE | lld:pubmed |
pubmed-article:10839289 | pubmed:author | pubmed-author:De LorenzoSS | lld:pubmed |
pubmed-article:10839289 | pubmed:author | pubmed-author:FabbrociniAA | lld:pubmed |
pubmed-article:10839289 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:10839289 | pubmed:volume | 82 | lld:pubmed |
pubmed-article:10839289 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:10839289 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:10839289 | pubmed:pagination | 1772-5 | lld:pubmed |
pubmed-article:10839289 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
pubmed-article:10839289 | pubmed:meshHeading | pubmed-meshheading:10839289... | lld:pubmed |
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pubmed-article:10839289 | pubmed:meshHeading | pubmed-meshheading:10839289... | lld:pubmed |
pubmed-article:10839289 | pubmed:year | 2000 | lld:pubmed |
pubmed-article:10839289 | pubmed:articleTitle | Gemcitabine combined with continuous infusion 5-fluorouracil in advanced and symptomatic pancreatic cancer: a clinical benefit-oriented phase II study. | lld:pubmed |
pubmed-article:10839289 | pubmed:affiliation | Cattedra di Oncologia Medica, Dipartimento di Endocrinologia ed Oncologia Molecolare a Clinica, Facoltà di Medicina e Chirurgia, Università Federico II, Napoli, Italy. | lld:pubmed |
pubmed-article:10839289 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:10839289 | pubmed:publicationType | Clinical Trial | lld:pubmed |
pubmed-article:10839289 | pubmed:publicationType | Clinical Trial, Phase II | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:10839289 | lld:pubmed |