Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2010-8-16
pubmed:abstractText
To estimate the safety and tolerability of daily administration of 250 mg of gefitinib given concurrently with three-dimensional conformal radiotherapy for patients with nonmetastatic prostate cancer.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1879-355X
pubmed:author
pubmed:copyrightInfo
Copyright (c) 2010 Elsevier Inc. All rights reserved.
pubmed:issnType
Electronic
pubmed:day
1
pubmed:volume
78
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
42-9
pubmed:meshHeading
pubmed-meshheading:20004525-Aged, pubmed-meshheading:20004525-Antineoplastic Agents, pubmed-meshheading:20004525-Combined Modality Therapy, pubmed-meshheading:20004525-Disease-Free Survival, pubmed-meshheading:20004525-Drug Administration Schedule, pubmed-meshheading:20004525-Humans, pubmed-meshheading:20004525-Interleukin-1alpha, pubmed-meshheading:20004525-Interleukin-6, pubmed-meshheading:20004525-Male, pubmed-meshheading:20004525-Maximum Tolerated Dose, pubmed-meshheading:20004525-Middle Aged, pubmed-meshheading:20004525-Neoplasm Proteins, pubmed-meshheading:20004525-Neoplasm Staging, pubmed-meshheading:20004525-Prostate-Specific Antigen, pubmed-meshheading:20004525-Prostatic Neoplasms, pubmed-meshheading:20004525-Quinazolines, pubmed-meshheading:20004525-Radiotherapy Dosage, pubmed-meshheading:20004525-Receptor, Epidermal Growth Factor, pubmed-meshheading:20004525-Tumor Necrosis Factor-alpha
pubmed:year
2010
pubmed:articleTitle
A phase I/II trial of gefitinib given concurrently with radiotherapy in patients with nonmetastatic prostate cancer.
pubmed:affiliation
Transplantation Laboratory and Haartman Institute and Finnish Institute for Molecular Medicine, University of Helsinki, Helsinki, Finland.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Clinical Trial, Phase II, Clinical Trial, Phase I