Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2006-10-18
pubmed:abstractText
To determine the feasibility, toxicity, and clinical effectiveness of concurrent weekly cisplatin chemotherapy in conjunction with definitive radiation in the treatment of localised muscle invasive bladder cancer.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0167-8140
pubmed:author
pubmed:issnType
Print
pubmed:volume
81
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
9-17
pubmed:dateRevised
2007-7-5
pubmed:meshHeading
pubmed-meshheading:17011058-Aged, pubmed-meshheading:17011058-Aged, 80 and over, pubmed-meshheading:17011058-Antineoplastic Agents, pubmed-meshheading:17011058-Carcinoma, Transitional Cell, pubmed-meshheading:17011058-Cisplatin, pubmed-meshheading:17011058-Combined Modality Therapy, pubmed-meshheading:17011058-Cystectomy, pubmed-meshheading:17011058-Epidemiologic Methods, pubmed-meshheading:17011058-Female, pubmed-meshheading:17011058-Humans, pubmed-meshheading:17011058-Male, pubmed-meshheading:17011058-Middle Aged, pubmed-meshheading:17011058-Neoplasm Invasiveness, pubmed-meshheading:17011058-Neoplasm Recurrence, Local, pubmed-meshheading:17011058-Radiation-Sensitizing Agents, pubmed-meshheading:17011058-Remission Induction, pubmed-meshheading:17011058-Salvage Therapy, pubmed-meshheading:17011058-Urinary Bladder Neoplasms
pubmed:year
2006
pubmed:articleTitle
Efficacy and tolerability of concurrent weekly low dose cisplatin during radiation treatment of localised muscle invasive bladder transitional cell carcinoma: a report of two sequential Phase II studies from the Trans Tasman Radiation Oncology Group.
pubmed:affiliation
Mater Radiation Oncology Centre, Princess Alexandra Hospital, Brisbane, Qld, Australia. Kumar_gogna@health.qld.gov.au
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Multicenter Study, Clinical Trial, Phase II