Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1992-9-2
pubmed:abstractText
Recombinant Interleukin 4 was administered by subcutaneous injection at daily doses of 0.5, 1.0 or 5.0 micrograms kg-1 to nine patients as part of a Phase I Dose Toxicity Study. Dose limiting toxicity was reached at 5 micrograms kg-1 day-1. Symptoms of toxicity included fatigue, 'flu like symptoms and elevated liver enzymes. Modest but significant elevations of neutrophil and platelet counts occurred. No clear evidence of antitumour effects emerged although pain in metastatic lymph nodes and a small fall in myeloma paraprotein levels during dosing were observed. In vitro and murine in vivo studies indicate that patients with lymphoproliferative disease should be selected for Phase II trials.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-2018830, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-2138559, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-2140512, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-2153452, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-2212677, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-2318249, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-2461987, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-2467815, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-2509916, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-2654291, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-2666563, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-2784419, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-2785856, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-2962580, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-3053902, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-3098893, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-3257252, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-3257976, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-3260922, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-3263554, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-3496417, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-3497196, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-3500261, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-6435125, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-6975300, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-6977612, http://linkedlifedata.com/resource/pubmed/commentcorrection/1637669-7459811
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0007-0920
pubmed:author
pubmed:issnType
Print
pubmed:volume
66
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
204-10
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1992
pubmed:articleTitle
Recombinant human interleukin 4 (IL-4) given as daily subcutaneous injections--a phase I dose toxicity trial.
pubmed:affiliation
Cancer Research Campaign, Department of Experimental Haematology, Christie Hospital NHS Trust, Manchester, U.K.
pubmed:publicationType
Journal Article, Clinical Trial