Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
1987-1-30
pubmed:abstractText
Fifteen patients with advanced malignancy were treated with escalating doses of recombinant beta ser 17 interferon (IFN). Doses ranging from 0.006 to 500 X 10(6) units/m2 were administered according to a dosage escalation scheme by iv push twice weekly (starting 1 week after an initial dose) for a planned minimum of 5 weeks, to be continued as a function of response. Toxic effects were broad in scope but generally low in grade. They included fever, malaise, leukopenia, proteinuria, nausea/vomiting, diarrhea, and mild elevations of serum transaminases and creatinine. In one patient, transient hypotension with bradycardia ensued. Malaise and fever increased somewhat with increasing dose. Doses of up to 500 X 10(6) units/m2 were tolerated without severe toxicity. A maximum tolerated dose was not defined. IFN pharmacokinetics followed a biphasic decay curve, with a distribution phase alpha-half-life of 9 minutes and an elimination phase beta-half-life of 103 minutes. Anti-IFN antibodies by the ELISA technique were present in seven of 15 patients. Presence of antibody did not correlate with toxicity or response. 2',5'-Adenylate synthetase levels were increased 2 and 24 hours after the initial dose, with a trend toward higher increments with higher doses. Minimal anti-tumor responses were seen in two patients with melanoma.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0361-5960
pubmed:author
pubmed:issnType
Print
pubmed:volume
70
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1365-72
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:3791249-2',5'-Oligoadenylate Synthetase, pubmed-meshheading:3791249-Adult, pubmed-meshheading:3791249-Aged, pubmed-meshheading:3791249-Antibodies, pubmed-meshheading:3791249-Drug Administration Schedule, pubmed-meshheading:3791249-Drug Evaluation, pubmed-meshheading:3791249-Drug-Induced Liver Injury, pubmed-meshheading:3791249-Female, pubmed-meshheading:3791249-Hematologic Diseases, pubmed-meshheading:3791249-Humans, pubmed-meshheading:3791249-Interferon Type I, pubmed-meshheading:3791249-Interferon-beta, pubmed-meshheading:3791249-Kidney Diseases, pubmed-meshheading:3791249-Kinetics, pubmed-meshheading:3791249-Lymphocytes, pubmed-meshheading:3791249-Male, pubmed-meshheading:3791249-Middle Aged, pubmed-meshheading:3791249-Nausea, pubmed-meshheading:3791249-Neoplasms, pubmed-meshheading:3791249-Recombinant Proteins
pubmed:year
1986
pubmed:articleTitle
Phase I study of recombinant beta ser 17 interferon in the treatment of cancer.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't