Autologous CD34(+) enriched peripheral blood progenitor cell (PBPC) transplantation is associated with higher morbidity in patients with lymphoma when compared to unmanipulated PBPC transplantation
J. Friedman et al., Autologous CD34(+) enriched peripheral blood progenitor cell (PBPC) transplantation is associated with higher morbidity in patients with lymphoma when compared to unmanipulated PBPC transplantation, BONE MAR TR, 26(8), 2000, pp. 831-836
Citations number
12
Categorie Soggetti
Hematology,"Medical Research Diagnosis & Treatment
High-dose chemotherapy followed by CD34(+) enriched peripheral blood progen
itor cell (PBPC) transplantation is used for the treatment of primary refra
ctory or relapsed Hodgkin's and non-Hodgkin's lymphomas, The CD34(+) enrich
ment procedure, while reducing tumor burden, may compromise immunological r
econstitution in the transplanted patient and result in increased rates of
post-transplant infection. We compared infectious complications in patients
with lymphoma who were treated with high-dose chemotherapy and supported e
ither with CD34(+) enriched PBPC (n = 19) or unmanipulated PBPCs (n = 24).
Analysis was limited to patients discharged from initial hospitalization fo
r transplantation with a minimum of 1 year followup and free of lymphoma re
currence. We found a statistically significant increase in the number of pa
tients with one or more infectious events in the CD34(+) transplant group (
14/19) compared with the unmanipulated PBPC group (9/24, P < 0.01). Greater
numbers of patients with two or more infectious events were observed in th
e CD34(+) group (7/19 vs 2/24, P < 0.03) and an increased incidence of bact
erial infections was observed in the CD34(+) group (10/19 vs 5/24, P < 0,05
). Two deaths due to infectious complications were observed in the CD34(+)
group. There was no significant difference in blood lymphocyte or monocyte
recovery between the groups. These data demonstrate a significant increase
in the long-term incidence of infectious events in lymphoma patients transp
lanted with autologous CD34(+) enriched PBPCs compared to unmanipulated PBP
Cs. Thus, patients who undergo CD34(+) enriched PBPC transplantation should
be followed closely for infectious complications and prolonged infectious
prophylaxis should be considered.