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Double-blind prospective randomized comparison of interferon gamma-1b versus placebo after autologous stem cell transplantation.

Author(s): Koziner B, Dengra C, Cisneros M, Glancszpigel R

Affiliation(s): Bone Marrow Transplant Unit, Clinica Independencia, Munro, Buenos Aires, Argentina. info@oncogroup.com.ar

Publication date & source: 2002, Acta Haematol., 108(2):66-73.

Publication type: Clinical Trial; Randomized Controlled Trial

Thirty-eight patients, including 14 with Hodgkin's disease, 9 with non-Hodgkin's lymphomas, 4 with multiple myeloma and 11 with solid tumors, were enrolled in our study. Between March 1995 and March 1997, 24 of these patients had been autografted with peripheral blood, and 14 had received peripheral blood autografts plus bone marrow. The study was a double-blind, prospectively randomized comparison of interferon gamma-1b (IFN-gamma), given subcutaneously at a dose of 50 microg/m(2) daily for 30 days to 18 of the 38 patients, vs. placebo (20 of 38). Administration started after 2 consecutive days of >0.5 x 10(9) neutrophils/l following autologous stem cell transplantation. At a mean follow-up time of 536 +/- 269 days, disease-free survival (DFS) for the IFN-gamma and placebo groups was 728 vs. 510 days, respectively (p < 0.0750 by the Generalized Wilcoxon/Peto-Prentice test). Overall survival (OS) time for the IFN-gamma and placebo groups was 830 vs. 755 days, respectively. Despite the limited number of patients included in this comparison, a trend for superior DFS was observed in the IFN-gamma-treated group, a finding which merits further study. Copyright 2002 S. Karger AG, Basel

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