Neutropenic infections in 100 patients with non-Hodgkin's lymphoma or Hodgkin's disease treated with high-dose BEAM chemotherapy and peripheral bloodprogenitor cell transplant: out-patient treatment is a viable option

Citation
S. Seropian et al., Neutropenic infections in 100 patients with non-Hodgkin's lymphoma or Hodgkin's disease treated with high-dose BEAM chemotherapy and peripheral bloodprogenitor cell transplant: out-patient treatment is a viable option, BONE MAR TR, 23(6), 1999, pp. 599-605
Citations number
24
Categorie Soggetti
Hematology,"Medical Research Diagnosis & Treatment
Journal title
BONE MARROW TRANSPLANTATION
ISSN journal
02683369 → ACNP
Volume
23
Issue
6
Year of publication
1999
Pages
599 - 605
Database
ISI
SICI code
0268-3369(199903)23:6<599:NII1PW>2.0.ZU;2-C
Abstract
A retrospective analysis was performed on 100 patients with non-Hodgkin's l ymphoma (NHL, n = 75) or Hodgkin's disease (HD, n = 25) who underwent perip heral blood progenitor cell transplant (PBPCT) following high-dose chemothe rapy (HDCT) with BCNU, etoposide, cytarabine and melphalan (BEAM) between M arch 1994 and June 1997, Following PBPCT and until engraftment all patients received oral ciprofloxacin and fluconazole, patients with positive Herpes simplex virus serology received acyclovir and 91 patients received filgras tim, The median days of neutropenia and days to an absolute neutrophil coun t (ANC) >500/mm(3) were 6 and 9, respectively. Febrile neutropenia occurred in 68 patients, Gram-positive bacteremia occurred in 14 patients. No gram- negative infections, invasive fungal infections, intensive care visits or d eaths occurred during the period of neutropenia or in the first 30 days fol lowing transplant. In multivariate logistic regression the risk of developm ent of any infection was associated only with the duration of neutropenia ( P = 0.02) and the risk of bacteremia was associated only with the number of CD34(+) cells infused (P = 0.046), Among 49 patients treated in the outpat ient setting, 14 (28%) were never admitted, High-dose chemotherapy with BEA M supported by PBPCT, prophylactic antibiotics and filgrastim resulted in a low incidence of infections and no acute mortality, WBC engraftment occurr ed rapidly allowing for a predictable course during which lengthy hospital stays and amphotericin therapy could be avoided.