EPO in combination with G-CSF improves mobilization effectiveness after chemotherapy with ifosfamide, epirubicin and etoposide and reduces costs during mobilization and transplantation of autologous hematopoietic progenitor cells

Hart, C. and Grassinger, J. and Andreesen, R. and Hennemann, Burkhard (2009) EPO in combination with G-CSF improves mobilization effectiveness after chemotherapy with ifosfamide, epirubicin and etoposide and reduces costs during mobilization and transplantation of autologous hematopoietic progenitor cells. BONE MARROW TRANSPLANTATION, 43 (3). pp. 197-206. ISSN 0268-3369, 1476-5365

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Abstract

A successful stem cell harvest is a prerequisite for peripheral blood SCT. We investigated the number of CD34(+) cells mobilized, the number of leukaphereses needed and the expenses of treatment for 28 patients with multiple myeloma randomly assigned to receive either G-CSF alone or G-CSF + EPO for stem cell mobilization after chemotherapy with ifosfamide, epirubicin and etoposide. All patients treated with G-CSF + EPO reached the threshold of 6 x 10(6) CD34(+) cells per kg body weight (kgbw), with a mean of 1.3 leukaphereses. On average 15.4 x 10(6) CD34(+) cells/kgbw were collected. In the G-CSF-alone group, the mean number of leukaphereses was 1.8, and 12.6 x 10(6) CD34(+) cells/kgbw were collected, and two patients failed the threshold. Overall costs per patient for mobilization and leukaphereses were (sic)8339 (G-CSF + EPO) and (sic)8842 (G-CSF). After transplantation, fewer blood transfusions (0.6 versus 1.3, P = 0.05), fewer days on antibiotics (2.3 versus 6.1, P = 0.02) and a shorter hospital stay (15.2 versus 17.8, P = 0.06) were noted in the G-CSF + EPO group resulting in a 19.2% reduction of costs for each transplant (P = 0.018). In summary, EPO improves the mobilization efficiency of G-CSF and so reduces costs of mobilization and SCT.

Item Type: Article
Uncontrolled Keywords: COLONY-STIMULATING FACTOR; HIGH-DOSE CHEMOTHERAPY; PERIPHERAL-BLOOD STEM; MULTIPLE-MYELOMA; BONE-MARROW; RANDOMIZED-TRIAL; MESSENGER-RNA; IN-VITRO; ERYTHROPOIETIN; CYCLOPHOSPHAMIDE; stem cells; mobilization; transplantation; erythropoietin; multiple myeloma
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Innere Medizin III (Hämatologie und Internistische Onkologie)
Depositing User: Dr. Gernot Deinzer
Date Deposited: 06 Oct 2020 10:48
Last Modified: 06 Oct 2020 10:48
URI: https://pred.uni-regensburg.de/id/eprint/29491

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