Blood stem cell collections after mobilization with combination chemotherapy containing ifosfamide followed by G-CSF in multiple myeloma
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vor 21 Jahren
High-dose chemotherapy with autologous peripheral blood stem cell
transplantation is the standard treatment of patients with multiple
myeloma today. In this study we used a combination mobilizing
chemotherapy containing ifosfamide with G-CSF before stem cell
collection. The chemotherapy regimen consisted of ifosfamide (2,500
mg/m(2) days 1-3), epirubicin (100 mg/m(2) day 1) and etoposide
(150 mg/m2 days 1-3) followed by G-CSF (5 mug/kg from day 5). In 30
younger patients (median age 51 years; range 41-60 years) who
received the IEV regimen in 100% dosage, a median of 11.15 x 10(6)
CD34(+) cells/kg (range 0-44.60 x 10(6) CD34(+) cells/kg) was
collected. In 22 elder patients (median age 64 years; range 59-72
years) similar collection results were obtained with a median of
10.82 x 10(6) CD34(+) cells/kg (range 0.99-42.22 x 10(6) CD34(+)
cells/kg) after the IEV regimen in 75% dosage. The pretreatment
chemotherapy cycles before mobilization were fewer in elder
patients with a median of 0 cycles (range 0-7 cycles) compared with
younger patients with a median of 4 cycles (range 0-7 cycles).
These collection results were favorable and allowed to support a
tandem transplantation procedure in younger and elder patients in
97 and 95%, respectively. In the majority of patients, the
hematological toxicity of IEV was of WHO grade 3/4. The
extramedullary toxicity was mild to moderate and there were only
few cases (5-10%) of relevant nephrotoxicity or neurotoxicity
associated with the application of ifosfamide. Copyright (C) 2003
S. Karger AG, Basel.
transplantation is the standard treatment of patients with multiple
myeloma today. In this study we used a combination mobilizing
chemotherapy containing ifosfamide with G-CSF before stem cell
collection. The chemotherapy regimen consisted of ifosfamide (2,500
mg/m(2) days 1-3), epirubicin (100 mg/m(2) day 1) and etoposide
(150 mg/m2 days 1-3) followed by G-CSF (5 mug/kg from day 5). In 30
younger patients (median age 51 years; range 41-60 years) who
received the IEV regimen in 100% dosage, a median of 11.15 x 10(6)
CD34(+) cells/kg (range 0-44.60 x 10(6) CD34(+) cells/kg) was
collected. In 22 elder patients (median age 64 years; range 59-72
years) similar collection results were obtained with a median of
10.82 x 10(6) CD34(+) cells/kg (range 0.99-42.22 x 10(6) CD34(+)
cells/kg) after the IEV regimen in 75% dosage. The pretreatment
chemotherapy cycles before mobilization were fewer in elder
patients with a median of 0 cycles (range 0-7 cycles) compared with
younger patients with a median of 4 cycles (range 0-7 cycles).
These collection results were favorable and allowed to support a
tandem transplantation procedure in younger and elder patients in
97 and 95%, respectively. In the majority of patients, the
hematological toxicity of IEV was of WHO grade 3/4. The
extramedullary toxicity was mild to moderate and there were only
few cases (5-10%) of relevant nephrotoxicity or neurotoxicity
associated with the application of ifosfamide. Copyright (C) 2003
S. Karger AG, Basel.
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