Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2011-2-22
pubmed:abstractText
Paclitaxel (PACL) plus gemcitabine (GEM) is an effective regimen for advanced breast cancer patients pretreated with anthracyclines. A prolonged GEM infusion at a fixed dose rate (FDR) of 10 mg/m²/min produces higher levels of intracellular active metabolites of GEM when compared with a standard 30-min infusion. In the present phase I/II trial, we investigated the association of FDR GEM plus PACL.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1432-0843
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
67
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
687-93
pubmed:meshHeading
pubmed-meshheading:20512334-Adult, pubmed-meshheading:20512334-Aged, pubmed-meshheading:20512334-Anthracyclines, pubmed-meshheading:20512334-Antineoplastic Combined Chemotherapy Protocols, pubmed-meshheading:20512334-BRCA1 Protein, pubmed-meshheading:20512334-Breast Neoplasms, pubmed-meshheading:20512334-Deoxycytidine, pubmed-meshheading:20512334-Disease-Free Survival, pubmed-meshheading:20512334-Drug Administration Schedule, pubmed-meshheading:20512334-Female, pubmed-meshheading:20512334-Humans, pubmed-meshheading:20512334-Middle Aged, pubmed-meshheading:20512334-Neoplasm Recurrence, Local, pubmed-meshheading:20512334-Paclitaxel, pubmed-meshheading:20512334-Survival, pubmed-meshheading:20512334-Time Factors, pubmed-meshheading:20512334-Treatment Outcome, pubmed-meshheading:20512334-Tumor Suppressor Proteins, pubmed-meshheading:20512334-Young Adult
pubmed:year
2011
pubmed:articleTitle
Phase I-II trial of prolonged gemcitabine infusion plus paclitaxel as a biweekly schedule for advanced breast cancer patients pretreated with anthracyclines.
pubmed:affiliation
Department of Medical Oncology, Regina Elena Cancer Institute, Rome, Italy. pvici@ifo.it
pubmed:publicationType
Journal Article, Comparative Study, Clinical Trial, Phase II, Clinical Trial, Phase I