Important note: Information in this article was accurate in 1993. The state of the art may have changed since the publication date.
Intermittent use of G-CSF in AIDS-related granulocytopenia (G) (Meeting abstract).
Ann Oncol; 3(Suppl 5):137 1992. Unique Identifier : AIDSLINE ICDB/93689689 Katz A; Levy GC; Albert Einstein Hosp., Sao Paulo, Brazil
Abstract:
AIDS patients (pts) often develop leukopenia and G, either related to the HIV infection itself or associated with the use of myelosuppressive drugs such as AZT or DHPG. This common event further complicates the clinical course of the pts and may require temporary or definitive discontinuation of these drugs. This problem might become especially distressful in pts with neurologic manifestations of AIDS receiving AZT. From March 1991 to November 1991, we treated 7 adult AIDS pts with AZT-induced G (WBC less than 2500 cells/mm3 and absolute neutrophil count [ANC] less than 1200 cells/mm3). Four pts had neurological manifestations of AIDS. Pts initially received daily sc G-CSF at 4-5 ug/kg, until adequate counts were achieved (WBC count greater than 5000/mm3 and ANC greater than 3000/mm3). CBC was always checked immediately before each administration of G-CSF. These counts were usually achieved after 2-4 days of therapy. At this point, pts started on a maintenance therapy which consisted of the intermittent administration of the minimum dose of G-CSF required to maintain adequate WBC and ANC. We found that all pts were capable of maintaining adequate counts while receiving G-CSF 2-3x a wk, at doses ranging from 150 to 300 ug/day. The use of G-CSF enabled us to use AZT at the same dose, it being before the onset of myelosuppression. The G of AIDS pts is not periodic and transient as the chemotherapy-related G, and therefore, special schedules of G-CSF will have to be devised for these pts.
Keywords: Acquired Immunodeficiency Syndrome/*DRUG THERAPY Agranulocytosis/CHEMICALLY INDUCED/*THERAPY Granulocyte Colony-Stimulating Factor/*THERAPEUTIC USE Human Zidovudine/ADVERSE EFFECTS/THERAPEUTIC USE ABSTRACT 930430
M9340818
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