The use of CD34(+)-selected PBPC after high-dose chemotherapy in breast cancer patients is associated with prolonged recovery time and increased infectious complications
M. Goerner et al., The use of CD34(+)-selected PBPC after high-dose chemotherapy in breast cancer patients is associated with prolonged recovery time and increased infectious complications, J HEMATH ST, 8(4), 1999, pp. 387-391
Citations number
16
Categorie Soggetti
Hematology,"Medical Research Diagnosis & Treatment
High-dose chemotherapy with autologous stem cell rescue can result in autot
ransplantation of tumor cells. A possible approach to reduce tumor cell con
tamination is the positive selection of CD34(+) PBPC, but this might be ass
ociated with a prolonged recovery time as well as an increased risk of infe
ctious complications because of the loss of committed progenitor cells. To
investigate this aspect, we compared two sequentially treated cohorts of hi
gh-risk breast cancer patients. Both groups received the same high-dose che
motherapy regimen followed by autologous peripheral stem cell transplantati
on. Group I received CD34(+)-selected blood progenitor cells, and group TI
received nonselected blood progenitor cells. We compared these two identica
lly treated groups with regard to recovery time, need for blood products, i
nfectious complications, need for antibiotic treatment, and length of the t
ransplantation-related hospital stay. We found a prolonged recovery time fo
r neutrophils up to 0.5 x 10(9)/L (14 days in the selected group/10 days in
the nonselected group) and platelets up to 30 x 10(9)/L (29/12 days), asso
ciated with an increased requirement for RBC transfusions (5/3 U) and plate
let transfusions (10/2 U). The rate of severe infectious complications (2/0
), the need for nonprophylactic antibiotic treatment (15/10), and the lengt
h of the hospital stay (25/21 days) in group I were also increased. We conc
lude that positive selection of PBPC should not be used routinely until ran
domized studies show a clear long-term benefit of using CD34(+)-selected st
em cell products in breast cancer patients.