Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2002-5-6
pubmed:abstractText
To determine the dose-limiting toxicity, maximum tolerated dose, and potential efficacy of irinotecan in children with refractory malignant solid tumors.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1077-4114
pubmed:author
pubmed:issnType
Print
pubmed:volume
24
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
94-100
pubmed:dateRevised
2011-10-6
pubmed:meshHeading
pubmed-meshheading:11990713-Adolescent, pubmed-meshheading:11990713-Adult, pubmed-meshheading:11990713-Antineoplastic Agents, Phytogenic, pubmed-meshheading:11990713-Bone Marrow Diseases, pubmed-meshheading:11990713-Camptothecin, pubmed-meshheading:11990713-Child, pubmed-meshheading:11990713-Child, Preschool, pubmed-meshheading:11990713-Diarrhea, pubmed-meshheading:11990713-Dose-Response Relationship, Drug, pubmed-meshheading:11990713-Drug-Induced Liver Injury, pubmed-meshheading:11990713-Enzyme Inhibitors, pubmed-meshheading:11990713-Female, pubmed-meshheading:11990713-Humans, pubmed-meshheading:11990713-Infusions, Intravenous, pubmed-meshheading:11990713-Japan, pubmed-meshheading:11990713-Leiomyosarcoma, pubmed-meshheading:11990713-Male, pubmed-meshheading:11990713-Maximum Tolerated Dose, pubmed-meshheading:11990713-Metabolic Clearance Rate, pubmed-meshheading:11990713-Neoplasm Proteins, pubmed-meshheading:11990713-Neuroblastoma, pubmed-meshheading:11990713-Neuroectodermal Tumors, Primitive, pubmed-meshheading:11990713-Topoisomerase I Inhibitors, pubmed-meshheading:11990713-Treatment Outcome
pubmed:year
2002
pubmed:articleTitle
Phase I study of irinotecan in pediatric patients with malignant solid tumors.
pubmed:affiliation
Study Group of Japan for Treatment of Advanced Neuroblastoma, Gunma.
pubmed:publicationType
Journal Article, Clinical Trial, Research Support, Non-U.S. Gov't, Multicenter Study, Clinical Trial, Phase I