Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2011-3-14
pubmed:abstractText
Gemcitabine based regimens have been widely used in patients with advanced cholangiocarcinoma (CC), but no standard therapy exists. In this study we aimed to find the maximally tolerated dose (MTD) of a two-week schedule of fixed dose rate (FDR) gemcitabine (G), oxaliplatin (O) and capecitabine (C), and evaluate the safety and efficacy of this regimen in patients with advanced cholangiocarcinoma (CC).
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1651-226X
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
50
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
448-54
pubmed:meshHeading
pubmed-meshheading:20670085-Adult, pubmed-meshheading:20670085-Aged, pubmed-meshheading:20670085-Antineoplastic Combined Chemotherapy Protocols, pubmed-meshheading:20670085-Bile Duct Neoplasms, pubmed-meshheading:20670085-Bile Ducts, Intrahepatic, pubmed-meshheading:20670085-Cholangiocarcinoma, pubmed-meshheading:20670085-Deoxycytidine, pubmed-meshheading:20670085-Disease Progression, pubmed-meshheading:20670085-Dose-Response Relationship, Drug, pubmed-meshheading:20670085-Drug Administration Schedule, pubmed-meshheading:20670085-Female, pubmed-meshheading:20670085-Fluorouracil, pubmed-meshheading:20670085-Humans, pubmed-meshheading:20670085-Male, pubmed-meshheading:20670085-Maximum Tolerated Dose, pubmed-meshheading:20670085-Middle Aged, pubmed-meshheading:20670085-Organoplatinum Compounds, pubmed-meshheading:20670085-Treatment Outcome
pubmed:year
2011
pubmed:articleTitle
A Phase I-II dose escalation study of fixed-dose rate gemcitabine, oxaliplatin and capecitabine every two weeks in advanced cholangiocarcinomas.
pubmed:affiliation
Department of Oncology, The Finsen Centre, Rigshospitalet, Copenhagen, Denmark. ulrik.lassen@rh.regionh.dk
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Multicenter Study, Clinical Trial, Phase II, Clinical Trial, Phase I