Document 2796 DOCN M94A2796 TI The role of hrGM-CSF in neutropenia due to the cytostatic or ganciclovir treatment. DT 9412 AU Szlavik J; Banhegyl D; Miskovits E; Gerlei Z; Saint Laszlo Hospital, Department of Immunology, Budapest,; Hungary. SO Int Conf AIDS. 1994 Aug 7-12;10(1):222 (abstract no. PB0316). Unique Identifier : AIDSLINE ICA10/94369779 AB OBJECTIVE: Identification of the role of human recombinant granulocyte-monocyte stimulating factor in neutropenia due to cytostatic treatment of Kaposi's sarcoma and non-Hodgkin's lymphoma associated with AIDS and that of the effectivity of hrGM-CSF in neutropenia due to ganciclovir treatment of cytomegalovirus retinitis. METHODS: Subcutaneous hrGM-CSF therapy (5 ug/kg/day) was applied for 7-17 days, after BACOD therapy in neutropenia of three patients with B-cell non-Hodgkin's lymphoma, while cytokine therapy in the same dose was applied in neutropenia of two patients with Kaposi's sarcoma due to BVA therapy. We tried to treat neutropenia due to inductive application of ganciclovir with a dose of 3-5 ug/kg/day of hrGM-CSF in eight patients with CMV retinitis. RESULTS: 13 patients (mean age: 32 years) were given 3-5 ug/kg/day sc. hrGM-CSF for 7-17 days (mean: 9.5). The initial neutrophil count 0.3-1.4 x 10(9)/l (mean: 0.7) increased to 1.8-9.3 x 10(9)/l (mean: 4.2) in the patients with KS and NHL as a result of treatment (mean CD4+: 102/mm3). There was a more significant increase in the neutrophil count in neutropenia due to ganciclovir treatment resulted by seven days treatment from the initial 0.8-2.1 x 10(9)/l (mean: 1.1) to 3.6-15.8 x 10(9)/l (mean: 4.2), (mean CD4+: 173/mm3). In the investigation period there was no infection observed in association with neutropenia, the main adverse effects of hrGM-CSF were fever in 7, fatigue and myalgia in 5 and confusion in 1 case. DISCUSSION: Cytokine therapy applied in combination is effective in neutropenia due to both the cytostatic treatment of tumours and ganciclovir treatment, infections associated with neutropenia can be prevented by it, although the effect depends on the initial CD4+ lymphocyte count of the patient. DE Adult Antineoplastic Agents, Combined/*ADVERSE EFFECTS/THERAPEUTIC USE Biological Response Modifiers/*THERAPEUTIC USE Bleomycins/ADMINISTRATION & DOSAGE/ADVERSE EFFECTS Cyclophosphamide/ADMINISTRATION & DOSAGE/ADVERSE EFFECTS Cytomegalovirus Retinitis/DRUG THERAPY Dexamethasone/ADMINISTRATION & DOSAGE/ADVERSE EFFECTS Doxorubicin/ADMINISTRATION & DOSAGE/ADVERSE EFFECTS Ganciclovir/*ADVERSE EFFECTS Granulocyte-Macrophage Colony-Stimulating Factor/*THERAPEUTIC USE Human HIV Infections/COMPLICATIONS Lymphoma, AIDS-Related/DRUG THERAPY Neutropenia/CHEMICALLY INDUCED/*THERAPY Recombinant Proteins/THERAPEUTIC USE Sarcoma, Kaposi's/DRUG THERAPY Vincristine/ADMINISTRATION & DOSAGE/ADVERSE EFFECTS MEETING ABSTRACT SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).