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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1989-2-23
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pubmed:abstractText |
Based on a preclinical study demonstrating the synergistic antitumor effect of recombinant interleukin 2 (rIL-2) and beta-interferon (IFN-beta) on mouse tumors and previous results of a phase I study of rIL-2, a phase I study of combination therapy with human rIL-2 and IFN-beta was conducted in 26 patients with advanced malignancy. Patients were given rIL-2 by 24-h continuous i.v. infusion and IFN-beta by 2-h i.v. infusion for 5 days each week for 4 weeks. The common side-effects were fever, malaise, chills, appetite loss, and diarrhea. Leukocytosis and eosinophilia were observed in 56% and 69% of the patients, respectively. Transient leukopenia and thrombocytopenia were also observed in some patients. Dose-limiting manifestations were intolerable fatigue and liver dysfunction, and it was concluded that the maximum tolerated doses of rIL-2 combined with IFN-beta were 1.1 x 10(6) U/m2/day for rIL-2 and 6.0 x 10(6) IU/m2/day for IFN-beta. No patients achieved complete and partial response to therapy in this study. One patient with pulmonary metastasis from pharyngeal cancer showed a minor response. Natural killer (NK) and lymphokine-activated killer (LAK) activities increased during the 5 days of treatment and decreased during the 2-day intermission. The percentage of IL-2 receptor-positive cells increased markedly until Day 12, and gradually decreased thereafter. The percentage of OKT 4-positive cells and the OKT 4/OKT 8 ratio increased. In contrast, the percentage of Leu 7- or Leu 11-positive cells decreased over the 4-week treatment. A phase II study of this combination therapy is ongoing against head and neck cancer, and renal cell carcinoma.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0008-5472
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
49
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
730-5
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:2783385-Adult,
pubmed-meshheading:2783385-Aged,
pubmed-meshheading:2783385-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:2783385-Cytotoxicity, Immunologic,
pubmed-meshheading:2783385-Drug Evaluation,
pubmed-meshheading:2783385-Female,
pubmed-meshheading:2783385-Humans,
pubmed-meshheading:2783385-Immunity, Cellular,
pubmed-meshheading:2783385-Interferon Type I,
pubmed-meshheading:2783385-Interleukin-2,
pubmed-meshheading:2783385-Lymphocytes,
pubmed-meshheading:2783385-Male,
pubmed-meshheading:2783385-Middle Aged,
pubmed-meshheading:2783385-Neoplasms,
pubmed-meshheading:2783385-Phenotype,
pubmed-meshheading:2783385-Recombinant Proteins
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pubmed:year |
1989
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pubmed:articleTitle |
Phase I study of combination therapy with interleukin 2 and beta-interferon in patients with advanced malignancy.
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pubmed:affiliation |
Department of Internal Medicine, National Cancer Center Hospital, Tokyo, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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