Source:http://linkedlifedata.com/resource/pubmed/id/11033837
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9 Suppl 8
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pubmed:dateCreated |
2001-1-3
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pubmed:abstractText |
Safety data from two randomized phase II and one abbreviated phase III placebo-controlled, double-blind clinical studies in adult patients with nonmyeloid malignancies indicate that recombinant human interleukin-11 (rhIL-11, also known as oprelvekin [Neumega]) has an acceptable toxicity profile as therapy for the mitigation of chemotherapy-induced thrombocytopenia. Preliminary data also indicate that rhIL-11 is well tolerated by pediatric patients with similar types of cancers. Adverse events associated with rhIL-11 are generally mild or moderate, reversible with drug discontinuation, and easily managed. Many of the common adverse events of rhIL-11--including edema, dyspnea, pleural effusions, conjunctival injection, and in some patients, atrial arrhythmia--occur in association with fluid retention. However, these adverse events can be medically managed and need not limit the use of rhIL-11, particularly if ameliorative measures, such as salt restriction and occasional prophylaxis with a potassium-sparing diuretic to minimize peripheral edema, have been instituted along with close monitoring of fluid and electrolyte status. Such measures are suggested for any patient treated with a diuretic, especially patients with cancer who are receiving multiple medications that complicate overall care. Administration of sequential cycles of rhIL-11 treatment does not appear to result in an increased incidence of adverse events or bone marrow exhaustion. rhIL-11 does not appear to interact adversely with concomitantly administered chemotherapeutic agents or agents commonly used for supportive care, including granulocyte colony-stimulating factor (G-CSF, filgrastim [Neu-pogen]).
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Colony-Stimulating Factors,
http://linkedlifedata.com/resource/pubmed/chemical/Drug Combinations,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-11,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/oprelvekin
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0890-9091
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
41-7
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:11033837-Antineoplastic Agents,
pubmed-meshheading:11033837-Arrhythmias, Cardiac,
pubmed-meshheading:11033837-Blood Platelets,
pubmed-meshheading:11033837-Colony-Stimulating Factors,
pubmed-meshheading:11033837-Double-Blind Method,
pubmed-meshheading:11033837-Drug Combinations,
pubmed-meshheading:11033837-Drug Interactions,
pubmed-meshheading:11033837-Dyspnea,
pubmed-meshheading:11033837-Edema,
pubmed-meshheading:11033837-Humans,
pubmed-meshheading:11033837-Hypokalemia,
pubmed-meshheading:11033837-Interleukin-11,
pubmed-meshheading:11033837-Platelet Activation,
pubmed-meshheading:11033837-Recombinant Proteins,
pubmed-meshheading:11033837-Safety,
pubmed-meshheading:11033837-Thrombocytopenia
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pubmed:year |
2000
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pubmed:articleTitle |
Tolerability and side-effect profile of rhIL-11.
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pubmed:affiliation |
Clinic Research Earle A. Chiles Research Institute, Providence Portland Medical Center, Oregon, USA. jsmith3@providence.org
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Randomized Controlled Trial,
Clinical Trial, Phase II,
Clinical Trial, Phase III
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