Phase I study of subcutaneously-administered bacterially-synthesised recombinant human granulocyte-macrophage colony-stimulating factor

G. K. Schwartz, D. Lehrer, Y. Baldwin, J. F. Holland, J. Mandeli, J. J. Collins, A. Galazka, P. A. Nessi

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Abstract

A phase I study was initiated to test the effect of bacterially-synthesised recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF). 15 patients with advanced cancers were entered into the study and 14 were evaluable. Patients were administered a single subcutaneous injection (3.0-300 μg/m2) of rhGM-CSF. Starting at a concentration of 100 μg/m2, an approximate 2-fold increase in leucocyte count was noted 24 h after the injection. By 48 h the counts had returned to baseline. The 300 μg/m2 concentration also induced an approximate 2-fold increase. The leucocytosis was associated with a predominant increase in circulating neutrophils and bands. An increase in monocytes was also noted, but peak levels were recorded 48-72 h after the injection. At both the 100 μg/m2 and the 300 μg/m2 doses, significant levels of circulating rhGM-CSF were detected. The levels measured in the plasma of patients receiving 300 μg/m2 were over 10-fold greater than those measured at 100 μg/m2. There was no detectable antibody formation against the rhGM-CSF in any of the study patients. The drug was exceptionally well-tolerated. This study shows that rhGM-CSF can be safely administered by subcutaneous administration and a single injection is capable of inducing a leucocytosis with increased circulating neutrophils, bands, and monocytes when doses are used which result in significant levels of circulating rhGM-CSF.

Original languageEnglish
Pages (from-to)470-473
Number of pages4
JournalEuropean Journal of Cancer
Volume28
Issue number2-3
DOIs
StatePublished - 1992

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