Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1997-2-27
pubmed:abstractText
Systemic fungal infections (SFI) in patients receiving high-dose chemotherapy (HDC) are a frequent cause of morbidity and mortality. Preclinical studies have reported augmented antifungal activity of monocytes, macrophage cells, and neutrophils exposed to certain colony-stimulating factors (CSF), including GM-CSF. We conducted a retrospective descriptive epidemiologic study to examine the characteristics of 145 consecutive patients receiving HDC administered with or without autologous stem cell transplantation (ASCT) and who subsequently received either GM-CSF and G-CSF, G-CSF alone, GM-CSF +/- IL-3 or no CSF. The analysis of this patient population sought to define the incidence of SFI and its relationship to therapy with monocyte/macrophage-stimulating (MMS group) cytokines (GM-CSF and G-CSF; GM-CSF +/- IL-3) or to cytokines which do not result in monocyte/macrophage stimulation (NMMS group, G-CSF alone or no CSF). Risk factors for the development of SFI were balanced between the MMS (n = 70) and NMMS (n = 75) groups. Two patients (2.9%) in the MMS and nine patients (12%) in the NMMS groups developed SFI. The risk ratio for developing SFI in the NMMS group compared to the MMS group was 4.20 (P = 0.023). This relationship was confounded, however, by the diagnosis of hematologic tumor or solid tumor (RR = 3.15, P = 0.082). SFI was the primary cause or major contributing factor in five of the 10 total deaths in our study population. Four SFI-related deaths occurred in the NMMS group and one SFI-related death occurred in the MMS group. Our data suggest a protective role for GM-CSF, IL-3 or other MMS cytokines in preventing SFI in patients receiving HDC. This should be further investigated as a potential complementary approach to conventional strategies in antifungal prophylaxis for patients receiving HDC.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0268-3369
pubmed:author
pubmed:issnType
Print
pubmed:volume
18
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
93-102
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:8832001-Adult, pubmed-meshheading:8832001-Aged, pubmed-meshheading:8832001-Aged, 80 and over, pubmed-meshheading:8832001-Antineoplastic Combined Chemotherapy Protocols, pubmed-meshheading:8832001-Bone Marrow Diseases, pubmed-meshheading:8832001-Disease Susceptibility, pubmed-meshheading:8832001-Female, pubmed-meshheading:8832001-Granulocyte Colony-Stimulating Factor, pubmed-meshheading:8832001-Granulocyte-Macrophage Colony-Stimulating Factor, pubmed-meshheading:8832001-Hematopoietic Stem Cell Transplantation, pubmed-meshheading:8832001-Humans, pubmed-meshheading:8832001-Immunity, Cellular, pubmed-meshheading:8832001-Incidence, pubmed-meshheading:8832001-Interleukin-3, pubmed-meshheading:8832001-Male, pubmed-meshheading:8832001-Middle Aged, pubmed-meshheading:8832001-Mycoses, pubmed-meshheading:8832001-Neoplasms, pubmed-meshheading:8832001-Recombinant Proteins, pubmed-meshheading:8832001-Retrospective Studies, pubmed-meshheading:8832001-Risk Factors
pubmed:year
1996
pubmed:articleTitle
Antifungal effects of yeast-derived rhu-GM-CSF in patients receiving high-dose chemotherapy given with or without autologous stem cell transplantation: a retrospective analysis.
pubmed:affiliation
Department of Pharmacy, Saint Louis University Hospital, MO 63110-0250, USA.
pubmed:publicationType
Journal Article, Review, Research Support, Non-U.S. Gov't