Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2010-5-3
pubmed:databankReference
pubmed:abstractText
Histone deacetylase (HDAC) inhibitors have shown radiosensitising activity in preclinical tumour models. This phase 1 study assessed the use of vorinostat combined with pelvic palliative radiotherapy for gastrointestinal carcinoma.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1474-5488
pubmed:author
pubmed:copyrightInfo
2010 Elsevier Ltd. All rights reserved.
pubmed:issnType
Electronic
pubmed:volume
11
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
459-64
pubmed:meshHeading
pubmed-meshheading:20378407-Aged, pubmed-meshheading:20378407-Aged, 80 and over, pubmed-meshheading:20378407-Colonic Neoplasms, pubmed-meshheading:20378407-Combined Modality Therapy, pubmed-meshheading:20378407-Dose-Response Relationship, Drug, pubmed-meshheading:20378407-Dose-Response Relationship, Radiation, pubmed-meshheading:20378407-Female, pubmed-meshheading:20378407-Gastrointestinal Neoplasms, pubmed-meshheading:20378407-Histone Deacetylase Inhibitors, pubmed-meshheading:20378407-Humans, pubmed-meshheading:20378407-Hydroxamic Acids, pubmed-meshheading:20378407-Male, pubmed-meshheading:20378407-Maximum Tolerated Dose, pubmed-meshheading:20378407-Middle Aged, pubmed-meshheading:20378407-Palliative Care, pubmed-meshheading:20378407-Pelvic Neoplasms, pubmed-meshheading:20378407-Rectal Neoplasms, pubmed-meshheading:20378407-Stomach Neoplasms
pubmed:year
2010
pubmed:articleTitle
Vorinostat, a histone deacetylase inhibitor, combined with pelvic palliative radiotherapy for gastrointestinal carcinoma: the Pelvic Radiation and Vorinostat (PRAVO) phase 1 study.
pubmed:affiliation
Department of Tumour Biology, Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway. a.h.ree@medisin.uio.no
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Clinical Trial, Phase I