Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
1996-9-6
pubmed:abstractText
Although high-dose interleukin-2 (IL-2) can produce durable remissions in a subset of responding patients with renal cell carcinoma (RCC), this occurs in the setting of significant toxicity. The purpose of this study is to define the maximum-tolerated dosage (MTD) of IL-2 and interferon alfa-2a (IFN alpha-2a) that can be administered chronically on an outpatient basis.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0732-183X
pubmed:author
pubmed:issnType
Print
pubmed:volume
14
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2234-41
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:8708712-Adult, pubmed-meshheading:8708712-Aged, pubmed-meshheading:8708712-Antineoplastic Agents, pubmed-meshheading:8708712-Biopterin, pubmed-meshheading:8708712-Carcinoma, Renal Cell, pubmed-meshheading:8708712-Cohort Studies, pubmed-meshheading:8708712-Female, pubmed-meshheading:8708712-Humans, pubmed-meshheading:8708712-Injections, Subcutaneous, pubmed-meshheading:8708712-Interferon-alpha, pubmed-meshheading:8708712-Interleukin-2, pubmed-meshheading:8708712-Kidney Neoplasms, pubmed-meshheading:8708712-Killer Cells, Natural, pubmed-meshheading:8708712-Male, pubmed-meshheading:8708712-Middle Aged, pubmed-meshheading:8708712-Neoplasms, pubmed-meshheading:8708712-Neopterin, pubmed-meshheading:8708712-Receptors, Interleukin-2, pubmed-meshheading:8708712-Recombinant Proteins, pubmed-meshheading:8708712-Remission Induction
pubmed:year
1996
pubmed:articleTitle
Phase I study of subcutaneously administered interleukin-2 in combination with interferon alfa-2a in patients with advanced cancer.
pubmed:affiliation
Division of Cancer Treatment, National Cancer Institute, Bethesda, MD, USA. bgause@mail.ncifcrf.gov
pubmed:publicationType
Journal Article, Clinical Trial, Clinical Trial, Phase I