Ap. Efremidis et al., PERIPHERAL-BLOOD PROGENITOR-CELL (PBPC) TRANSPLANTATION WITH A SINGLEAPHERESIS IN PATIENTS WITH LYMPHOMA, MYELOMA AND SOLID TUMORS, European journal of haematology, 57(4), 1996, pp. 269-277
The aim of this study was to investigate if a single apheresis after p
eripheral blood progenitor cell (PBPC) mobilization can be used to res
cue patients receiving high dose chemotherapy (HD.CHE) as treatment fo
r an underlying malignancy. Eighteen consecutive patients who were adm
itted to the transplant unit for treatment were leukapheresed followin
g mobilization with one of the following protocols: group I: rHuG-CSF
alone, group II: conventional chemotherapy (C.CHE)+rHuG-CSF or rHuGM-C
SF and group III: high dose cytoxan (HD.CTX)+rHuG-CSF. The optimal day
for leukapheresis was determined by following white blood cell counts
(WBC), mononuclear cell counts (MNC) and CD34(+) cell counts daily. G
ranulocyte-macrophage colony-forming cells (GM-CFC) assay was performe
d at the leukapheresis product and prior to reinfusion. All patients p
roceeded directly to ablative therapy according to their underlying ma
lignancy. PBPC from single apheresis were reinfused to all patients an
d cytokines started 24 h after infusion. Hematologic recovery after HD
.CHE was the parameter used to ensure successful engraftment. We have
been able to recover adequate number of PBPC for transplantation with
a single apheresis in all patients. The number of infused cells were f
or groups I, II and III: (I) median number of MNC 4.7, 3.58 and 2.79 x
10(8)/kg, respectively (2); median number of CD34(+) cells 4.4, 2.8,
2.7 x 10(6)/kg, respectively. The median apheresis day was 6, 16 and 1
6, respectively. Recovery times to granulocyte count >0.5 x 10(9)/L wa
s 9 d (range 9-12) and to platelets >20 x 10(9)/L was 12 d (range 1-13
5); 17/18 patients have engrafted successfully independent of the mobi
lization method used. These data suggest that sufficient PBPC can be h
arvested at a single leukapheresis for hemopoietic rescue after myeloa
blative therapy. Rapid hematologic recovery occurs when cytokines alon
e after conventional or HD.CHE are used for mobilization. Results of c
ollection products and hematopoietic recovery are independent of the m
obilization technique used.