Granulocyte Colony-Stimulating Factor in Severe Chemotherapy-Induced Afebrile Neutropenia
Lynn C. Hartmann, M.D., Loren K. Tschetter, M.D., Thomas M. Habermann, M.D., Larry P. Ebbert, M.D., P. Steven Johnson, M.D., James A. Mailliard, M.D., Ralph Levitt, M.D., Vera J. Suman, Ph.D., Thomas E. Witzig, M.D., H.S. Wieand, Ph.D., Langdon L. Miller, M.D., Charles G. Moertel, M.D., Darryl C. Grendahl, B.S.Pharm., and Dianne M. Herrera, R.N.
Background Randomized trials of colony-stimulating factors infebrile patients with neutropenia after chemotherapy have notconsistently shown clinical benefit. Nevertheless, the use ofcolony-stimulating factors to treat patients with chemotherapy-inducedneutropenia is widespread.
Methods We performed a randomized, double-blind, placebo-controlledtrial of granulocyte colony-stimulating factor (G-CSF) in afebrileoutpatients with severe chemotherapy-induced neutropenia. Wemeasured the number of days of neutropenia, rate of hospitalization,number of days in the hospital, number of days the patient receivedparenteral antibiotics, and number of culture-positive infections.
Results We randomly assigned 138 patients to receive G-CSF (n= 71) or placebo (n = 67). The median time to an absolute neutrophilcount higher than 500 per cubic millimeter was significantlyshorter for patients who received G-CSF (two days, vs. fourdays for the patients given placebo). However, there was noeffect on the rate of hospitalization, number of days in thehospital, duration of treatment with parenteral antibiotics,or number of culture-positive infections.
Conclusions Routine therapeutic application of G-CSF in afebrilepatients with severe neutropenia can reduce the duration ofneutropenia, but this does not appear to provide practical clinicalbenefit.
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