Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2002-8-14
pubmed:abstractText
The cisplatin and gemcitabine (GC) regimen is usually administered as a 4- or 3-week schedule; however, the best schedule to use is still unclear. We therefore started a randomized phase II trial to compare toxicity and dose intensity (DI) between these two GC schedules.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0923-7534
pubmed:author
pubmed:issnType
Print
pubmed:volume
13
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1080-6
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:12176787-Adult, pubmed-meshheading:12176787-Aged, pubmed-meshheading:12176787-Antineoplastic Combined Chemotherapy Protocols, pubmed-meshheading:12176787-Carcinoma, Non-Small-Cell Lung, pubmed-meshheading:12176787-Cisplatin, pubmed-meshheading:12176787-Confidence Intervals, pubmed-meshheading:12176787-Deoxycytidine, pubmed-meshheading:12176787-Dose-Response Relationship, Drug, pubmed-meshheading:12176787-Drug Administration Schedule, pubmed-meshheading:12176787-Female, pubmed-meshheading:12176787-Follow-Up Studies, pubmed-meshheading:12176787-Humans, pubmed-meshheading:12176787-Lung Neoplasms, pubmed-meshheading:12176787-Male, pubmed-meshheading:12176787-Maximum Tolerated Dose, pubmed-meshheading:12176787-Middle Aged, pubmed-meshheading:12176787-Neoplasms, pubmed-meshheading:12176787-Reference Values, pubmed-meshheading:12176787-Survival Analysis, pubmed-meshheading:12176787-Treatment Outcome
pubmed:year
2002
pubmed:articleTitle
Three-week versus four-week schedule of cisplatin and gemcitabine: results of a randomized phase II study.
pubmed:affiliation
Department of Medical Oncology and Hematology and Division of Thoracic Surgery, Istituto Clinico Humanitas, Rozzano-Milan, Italy. hector.sotoparra@humanitas.it
pubmed:publicationType
Journal Article, Clinical Trial, Comparative Study, Randomized Controlled Trial, Clinical Trial, Phase II