Autologous peripheral blood stem cell transplantation in patients with relapsed lymphoma results in accelerated haematopoietic reconstitution, improved quality of life and cost reduction compared with bone marrow transplantation: the Hovon 22 study
E. Vellenga et al., Autologous peripheral blood stem cell transplantation in patients with relapsed lymphoma results in accelerated haematopoietic reconstitution, improved quality of life and cost reduction compared with bone marrow transplantation: the Hovon 22 study, BR J HAEM, 114(2), 2001, pp. 319-326
The present study analysed whether autologous peripheral blood stem cell tr
ansplantation (PSCT) improves engraftment, quality of life and cost-effecti
veness when compared with autologous bone marrow transplantation (ABMT). Re
lapsing progressive lymphoma patients (n = 204; non-Hodgkin's lymphoma n =
166; Hodgkin's disease n = 38) were, after induction treatment with the DHA
P-VIM (cisplatin, cytarabine, dexamethasone, etoposide, ifosfamide, methotr
exate) regimen, randomly (2:1) assigned to the harvest of granulocyte-macro
phage colony-stimulating factor-mobilized stem cells after the second DHAP
course or autologous bone marrow cells before the second DHAP course. These
stem cells were reinfused following high-dose myeloblative chemotherapy. A
fter induction, 118 patients obtained a partial or complete response and we
re eligible for randomization. In the PSCT arm (n = 76) significantly faste
r engraftment of neutrophils [greater than or equal to 0.1 and; greater tha
n or equal to 0.5 x 10(9)/l: 10.7 d (7-36, median, range), 15 (9-45) versus
13 (8-25) and 26 (14-80), P < 0.01] and thrombocytes [<greater than or equ
al to> 20 x 10(9)/l: 13 d (7-51) versus 18 (11-65), P < 0.01] were observed
. In addition, significantly fewer transfusions of red blood cells [6 (0-23
) versus 8 (2-24), P < 0.01] and platelets [4 (0-60) versus 8 (2-55), P = 0
.01] were required in the PSCT arm. These findings were associated with a s
ignificant reduction in the median days of intravenous antibiotics in patie
nts with fever [8.5 (0-30) versus 14 (0-34), P = 0.04] and hospital stay [2
7 (8-51) versus 34 (24-78), P < 0.05]. Quality of life demonstrated a signi
ficant difference in favour of the PSCT arm. Total transplantation costs we
re significantly lower in the PSCT arm [$13 954 ($4913- 29 532) versus $17
668 ($10 170-44 083) P < 0.05], as a result of the reduced hospital stay an
d lower antibiotic costs. In summary, these results indicate that PSCT is s
uperior to ABMT with regard to engraftment, supportive care, quality of lif
e and cost.