rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
11
|
pubmed:dateCreated |
2000-7-6
|
pubmed:abstractText |
To determine the maximum-tolerated dose (MTD) and the dose-limiting toxicities (DLTs) of the raltitrexed plus oxaliplatin combination regimen, to explore its safety and pharmacokinetics, and to assess its antitumor activity in patients with advanced solid tumors.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
0732-183X
|
pubmed:author |
pubmed-author:ArmandJ PJP,
pubmed-author:BonnayMM,
pubmed-author:DanielCC,
pubmed-author:DucreuxMM,
pubmed-author:FandiAA,
pubmed-author:FizaziKK,
pubmed-author:HillCC,
pubmed-author:PoterreMM,
pubmed-author:RuffiéPP,
pubmed-author:SmithMM,
pubmed-author:SoriaJ CJC
|
pubmed:issnType |
Print
|
pubmed:volume |
18
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
2293-300
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:10829050-Adult,
pubmed-meshheading:10829050-Aged,
pubmed-meshheading:10829050-Antimetabolites, Antineoplastic,
pubmed-meshheading:10829050-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:10829050-Area Under Curve,
pubmed-meshheading:10829050-Dose-Response Relationship, Drug,
pubmed-meshheading:10829050-Female,
pubmed-meshheading:10829050-Humans,
pubmed-meshheading:10829050-Male,
pubmed-meshheading:10829050-Middle Aged,
pubmed-meshheading:10829050-Neoplasms,
pubmed-meshheading:10829050-Organoplatinum Compounds,
pubmed-meshheading:10829050-Quinazolines,
pubmed-meshheading:10829050-Thiophenes,
pubmed-meshheading:10829050-Treatment Outcome
|
pubmed:year |
2000
|
pubmed:articleTitle |
Phase I, dose-finding, and pharmacokinetic study of raltitrexed combined with oxaliplatin in patients with advanced cancer.
|
pubmed:affiliation |
Institut Gustave-Roussy, Villejuif, and AstraZeneca Pharmaceuticals, Cergy, France. fizazi@igr.fr
|
pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, Non-U.S. Gov't,
Clinical Trial, Phase I
|