Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:9120545rdf:typepubmed:Citationlld:pubmed
pubmed-article:9120545lifeskim:mentionsumls-concept:C0087111lld:lifeskim
pubmed-article:9120545lifeskim:mentionsumls-concept:C0017638lld:lifeskim
pubmed-article:9120545lifeskim:mentionsumls-concept:C0205282lld:lifeskim
pubmed-article:9120545lifeskim:mentionsumls-concept:C0015133lld:lifeskim
pubmed-article:9120545lifeskim:mentionsumls-concept:C0079083lld:lifeskim
pubmed-article:9120545lifeskim:mentionsumls-concept:C0034897lld:lifeskim
pubmed-article:9120545lifeskim:mentionsumls-concept:C0004083lld:lifeskim
pubmed-article:9120545lifeskim:mentionsumls-concept:C0282460lld:lifeskim
pubmed-article:9120545lifeskim:mentionsumls-concept:C0441938lld:lifeskim
pubmed-article:9120545pubmed:issue2lld:pubmed
pubmed-article:9120545pubmed:dateCreated1997-4-23lld:pubmed
pubmed-article:9120545pubmed:abstractTextThirty one patients previously treated with surgery, radiation therapy and chemotherapy with a nitrosourea for malignant supratentorial gliomas received a combination of carboplatin (CBDCA) and etoposide (VP16) at tumor progression. Carboplatin and etoposide (CE) were given, each at a dose of 100 mg/m2/day from day 1 to 3. The response was evaluated at each course and a minimum of three course was required to definite stable patient. Tolerance was evaluated in 31 patients. None had renal or auditory toxicity. Side effects consisted of grade III hematologic toxicity in 6 patients (19%), and grade III hepatic toxicity in one patient. No grade IV WHO toxicity was observed. All 31 patients could be evaluated for therapeutic response. A partial response was noted in 4 patients during 13, 34 +, 35 + and 51 + weeks. Ten patients had stable disease after a minimum of 3 courses (19 to 37 weeks). The rate of partial response (PR) and stabilisation (S) was 45% (14/31). The median time to tumor progression (MTTP) for responding and stable patients was 28 weeks. The median survival time (ST) for the entire group was 45 weeks and over 51 weeks for PR and S patients.lld:pubmed
pubmed-article:9120545pubmed:languageenglld:pubmed
pubmed-article:9120545pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:9120545pubmed:citationSubsetIMlld:pubmed
pubmed-article:9120545pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:9120545pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:9120545pubmed:statusMEDLINElld:pubmed
pubmed-article:9120545pubmed:monthAprlld:pubmed
pubmed-article:9120545pubmed:issn0167-594Xlld:pubmed
pubmed-article:9120545pubmed:authorpubmed-author:PoissonMMlld:pubmed
pubmed-article:9120545pubmed:authorpubmed-author:ChauveincLLlld:pubmed
pubmed-article:9120545pubmed:authorpubmed-author:DelattreJ YJYlld:pubmed
pubmed-article:9120545pubmed:authorpubmed-author:ChenQ MQMlld:pubmed
pubmed-article:9120545pubmed:authorpubmed-author:AmeriAAlld:pubmed
pubmed-article:9120545pubmed:issnTypePrintlld:pubmed
pubmed-article:9120545pubmed:volume32lld:pubmed
pubmed-article:9120545pubmed:ownerNLMlld:pubmed
pubmed-article:9120545pubmed:authorsCompleteYlld:pubmed
pubmed-article:9120545pubmed:pagination155-60lld:pubmed
pubmed-article:9120545pubmed:dateRevised2006-4-24lld:pubmed
pubmed-article:9120545pubmed:meshHeadingpubmed-meshheading:9120545-...lld:pubmed
pubmed-article:9120545pubmed:meshHeadingpubmed-meshheading:9120545-...lld:pubmed
pubmed-article:9120545pubmed:meshHeadingpubmed-meshheading:9120545-...lld:pubmed
pubmed-article:9120545pubmed:meshHeadingpubmed-meshheading:9120545-...lld:pubmed
pubmed-article:9120545pubmed:meshHeadingpubmed-meshheading:9120545-...lld:pubmed
pubmed-article:9120545pubmed:meshHeadingpubmed-meshheading:9120545-...lld:pubmed
pubmed-article:9120545pubmed:meshHeadingpubmed-meshheading:9120545-...lld:pubmed
pubmed-article:9120545pubmed:meshHeadingpubmed-meshheading:9120545-...lld:pubmed
pubmed-article:9120545pubmed:meshHeadingpubmed-meshheading:9120545-...lld:pubmed
pubmed-article:9120545pubmed:meshHeadingpubmed-meshheading:9120545-...lld:pubmed
pubmed-article:9120545pubmed:meshHeadingpubmed-meshheading:9120545-...lld:pubmed
pubmed-article:9120545pubmed:meshHeadingpubmed-meshheading:9120545-...lld:pubmed
pubmed-article:9120545pubmed:meshHeadingpubmed-meshheading:9120545-...lld:pubmed
pubmed-article:9120545pubmed:year1997lld:pubmed
pubmed-article:9120545pubmed:articleTitleTreatment of recurrent malignant supratentorial gliomas with the association of carboplatin and etoposide: a phase II study.lld:pubmed
pubmed-article:9120545pubmed:affiliationDepartment of Neurology Hôpital de la Pitté Salpêtrière, Paris, France.lld:pubmed
pubmed-article:9120545pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9120545pubmed:publicationTypeClinical Triallld:pubmed
pubmed-article:9120545pubmed:publicationTypeClinical Trial, Phase IIlld:pubmed