THE ADDITIVE EFFECT OF PERIPHERAL-BLOOD STEM-CELLS, HARVESTED WITH LOW-DOSE CYCLOPHOSPHAMIDE, TO AUTOLOGOUS BONE-MARROW REINFUSION ON HEMATOPOIETIC RECONSTITUTION AFTER ABLATIVE CHEMOTHERAPY IN BREAST-CANCER PATIENTS WITH LOCALIZED DISEASE
H. Degraaf et al., THE ADDITIVE EFFECT OF PERIPHERAL-BLOOD STEM-CELLS, HARVESTED WITH LOW-DOSE CYCLOPHOSPHAMIDE, TO AUTOLOGOUS BONE-MARROW REINFUSION ON HEMATOPOIETIC RECONSTITUTION AFTER ABLATIVE CHEMOTHERAPY IN BREAST-CANCER PATIENTS WITH LOCALIZED DISEASE, Anticancer research, 15(6B), 1995, pp. 2851-2856
The additive effect of peripheral blood stem cells (PBSCs) to autologo
us bone man ow transplantation (ABMT) on haematopoietic reconstitution
, after ablative chemotherapy in patients with locally advanced breast
cancer, was evaluated. Patients were treated with induction chemother
apy, followed by ablative chemotherapy consisting of mitoxantrone and
thiotepa. Group I (n=14) received ABMT and granulocyte macrophage-colo
ny stimulating factor (GM-CSF), group II (n=11) received ABMT, PBSCs a
nd granulocyte-colony stimulating factor. (G-CSF). PBSCs were harveste
d after a low-dose cyclophosphamide (750 mg/m(2)), followed by G-CSF.
Stern cell harvest was routinely started 12 days after cyclophosphamid
e. Compared to group I, group II showed a significant reduction in the
median number of days for leukocytes < 0.5 x 10(9)/L 4.5 days, leukoc
ytes < 1.0 x 10(9) / l 5.5 days, platelets < 20 x 10(9) / l 9 days and
platelets < 40 x 10(9) / l 12.5 days. The median number of transfusio
ns of platelets fell from 11.5 to 7 and of red blood cells from 8.5 to
6. The median hospitalisation duration declined from 40.5 to 30 days,
fever above 38 degrees C with 7.5 days, fever above 38.5 degrees C wi
th 4 days and antibiotic treatment with 8.5 days in group I versus gro
up II. Improvement of haematological recovery, duration of fever and h
ospitalisation was observed by the addition of PBSCs, obtained after a
relatively low-dose cyclophosphamide and G-CSF and stem cell pheresis
on fixed days, to autologous bone marrow and growth factor in the per
iod after ablative chemotherapy.