Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2010-12-20
pubmed:abstractText
OVA-301 is a large randomized trial that showed superiority of trabectedin plus pegylated liposomal doxorubicin (PLD) over PLD alone in relapsed ovarian cancer. The optimal management of patients with partially platinum-sensitive relapse [6-12 months platinum-free interval (PFI)] is unclear.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1569-8041
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
22
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
39-48
pubmed:meshHeading
pubmed-meshheading:20643862-Adult, pubmed-meshheading:20643862-Aged, pubmed-meshheading:20643862-Aged, 80 and over, pubmed-meshheading:20643862-Antineoplastic Combined Chemotherapy Protocols, pubmed-meshheading:20643862-Dioxoles, pubmed-meshheading:20643862-Disease-Free Survival, pubmed-meshheading:20643862-Doxorubicin, pubmed-meshheading:20643862-Drug Administration Schedule, pubmed-meshheading:20643862-Female, pubmed-meshheading:20643862-Humans, pubmed-meshheading:20643862-Middle Aged, pubmed-meshheading:20643862-Multivariate Analysis, pubmed-meshheading:20643862-Organoplatinum Compounds, pubmed-meshheading:20643862-Ovarian Neoplasms, pubmed-meshheading:20643862-Polyethylene Glycols, pubmed-meshheading:20643862-Recurrence, pubmed-meshheading:20643862-Tetrahydroisoquinolines, pubmed-meshheading:20643862-Treatment Outcome
pubmed:year
2011
pubmed:articleTitle
Trabectedin plus pegylated liposomal doxorubicin in relapsed ovarian cancer: outcomes in the partially platinum-sensitive (platinum-free interval 6-12 months) subpopulation of OVA-301 phase III randomized trial.
pubmed:affiliation
Area of Gynecologic Oncology, Valencian Institute of Oncology, Valencia, Spain. apoveda@fivo.org
pubmed:publicationType
Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't, Multicenter Study, Clinical Trial, Phase III