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Chinese Journal of Hematology ; (12): 462-465, 2004.
Article in Chinese | WPRIM | ID: wpr-291397

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate the efficacy of mitoxantrone combined high dose of cytarabine and recombinant human granulocyte colony-stimulating factor (MAG) regimen for mobilizing autologous peripheral blood stem cells (APBSC) in patients with hematopoietic malignancies.</p><p><b>METHODS</b>From December 1995 to April 2003, 14 lymphoma and 29 acute leukemia patients were treated with high-dose cytarabine (2 g/m2 every 12 h, days 1 and 2) and mitoxantrone (10 mg/m2, days 2 and 3), followed by 300 microgram recombinant human granulocyte colony-stimulating factor per day (rhG-CSF 300 microg/d) i.e, the MAG regimen as mobilization regimen of peripheral blood stem cells. rhG-CSF was given subcutaneously when the white blood cell (WBC) count below 1.0 x 10(9)/L following the MA chemotherapy, APBSC were harvested when WBC count increased using Baxter CS3000plus or Cobe Spectra.</p><p><b>RESULTS</b>Mobilization was successful in 13 of 14 lymphoma patients with MNC (3.91 +/- 2.70) x 10(8)/kg, CD34+ cells (17.79 +/- 12.90) x 10(6)/kg. Meanwhile, mobilization was successful in 24 of 29 acute leukemia patients with average of 2.13 times for apheresis. The median MNC and CD34+ cells yielded were 3.62 x 10(8)/kg and 7.37 x 10(6)/kg respectively, rhG-CSF was used for a median time of 7 days. Excepting for grade I-II gastrointestinal toxicity in 8 and infection in 14 cases, no major side effects were observed. There was no mobilization-related mortality. Minimal residual diseases became undetectable after mobilization in some patients.</p><p><b>CONCLUSION</b>MAG is a safe and highly effective mobilization regimen in patients with lymphoma and acute leukemia.</p>


Subject(s)
Adolescent , Adult , Female , Humans , Male , Middle Aged , Antineoplastic Combined Chemotherapy Protocols , Therapeutic Uses , Cytarabine , Granulocyte Colony-Stimulating Factor , Hematopoietic Stem Cell Mobilization , Methods , Hematopoietic Stem Cell Transplantation , Hematopoietic Stem Cells , Lymphoma , Therapeutics , Mitoxantrone , Precursor Cell Lymphoblastic Leukemia-Lymphoma , Therapeutics , Recombinant Proteins
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