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Pharmacokinetics and tolerance of intravenous and intramuscular recombinant alpha 2 interferon in patients with malignancies
Author(s) -
Shah I.,
Band J.,
Samson M.,
Young J.,
Robinson R.,
Bailey B.,
Lerner A. Martin,
Prasad A. S.
Publication year - 1984
Publication title -
american journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.456
H-Index - 105
eISSN - 1096-8652
pISSN - 0361-8609
DOI - 10.1002/ajh.2830170406
Subject(s) - chills , medicine , myalgia , pharmacokinetics , interferon , intramuscular injection , alpha interferon , gastroenterology , titer , interferon alfa , recombinant dna , route of administration , pharmacology , anesthesia , surgery , immunology , antibody , biochemistry , chemistry , gene
Fifteen patients with advanced hematopoietic and other malignancies were treated with recombinant DNA produced Alpha 2 Interferon (IFN) (Schering) by intravenous (IV) and intramuscular (IM) routes at weekly intervals in escalating doses from 1 × 10 6 IU to 100 × 10 6 IU in order to determine the tolerance and pharmacokinetics. The most common side effects included fever, chills, myalgia, and arthralgia. At doses of 60 × 10 6 or above, severe but reversible hypotension was observed in five patients receiving interferon by intravenous route. Patients receiving interferon by intramuscular route had fever, chills, and myalgias but did not develop hypotension at the same dosage. Two patients with non‐Hodgkin lymphoma showed objective evidence of regression. Our data suggest a biphasic pattern of elimination with terminal half‐life ranging from 1.9 to 2.9 hours and peak titer of 16,000 units and under for IV interferon, and terminal half‐life of 6 hours with peak titers of 600 units for intramuscular interferon. However, interpatient variability precludes a definite conclusion. Although the areas under the serum concentration vs time curves were similar, the intravenous route provided higher but unsustained levels of interferon than the intramuscular route.