Unmodified allogeneic peripheral blood stem cell transplantation (alloPBSCT
) was performed in 20 consecutive acute non-lymphoblastic leukemia (ANLL) p
atients from their HLA-identical siblings. There were 11 males and 9 female
s. Median age was 34 years (range 17-43). Donors were primed with 25-15 mu
g/kg/day s.c. granulocyte-colony stimulating factor (G-CSF, Neupogen, Roche
). Conditioning regimen was Bu (16 mg/kg) + Cy (120 mg/kg) in 19 patients a
nd high dose Ara-C (3 gr/m(2) twice daily for 3 days) for one patient who r
elapsed after bone marrow transplantation. Eighteen patients were in CR1. C
sA + short-term MTX (n=19) or CsA alone (n=1) were used for graft versus ho
st disease (GVHD) prophylaxis. The median number of apheresis procedures fo
r each patient was 2 (2-4). A median of 6.5 (3.2-38.2) x 10(8)/kg MNC or 9.
4 (2.2-12.4) x 10(6)/kg CD34+ cells were given. Median days to reach granul
ocyte of >0.5 x 10(9)/l and platelet of >50 x 10(9)/l were 12 (10-14) and 1
5 (11-35) respectively. Day 100 transplant-related mortality was 20 per cen
t (4/20). Grade 2 to 4 AGVHD was seen in 8 out of 17 (47%) evaluable patien
ts. Severe AGVHD occurred in 3 out of 17 (18%). Clinical CGVHD of all grade
s developed in 12 out of 17 (70%) evaluable patients. The mean disease-free
survival and overall survival were 17 (range: 8-33 months) and 18 months (
range: 10-34 months), respectively. In conclusion, alloPBSCT in ANLL is ass
ociated with a faster engraftment, no greater incidence of AGVHD, but incre
ased risk of CGVHD. Copyright (C) 1998 John Wiley & Sons, Ltd.