Increased Efficacy of Stem Cell Chemomobilization with Intermediate-Dose Cytarabine Plus Granulocyte Colony-Stimulating Factor (G-CSF) Compared with G-CSF Alone in Patients with Multiple Myeloma: Results of a Randomized Trial

•We provide the first evidence for the advantage of chemomobilization over granulocyte colony-stimulating factor (G-CSF).•An intermediate-dose cytarabine regimen is more efficient in terms of a greater proportion of patients achieving a CD34+ cell yield sufficient for tandem autologous stem cell tra...

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Veröffentlicht in:Biology of blood and marrow transplantation 2019-02, Vol.25 (2), p.248-255
Hauptverfasser: Czerw, Tomasz, Sadus-Wojciechowska, Maria, Michalak, Katarzyna, Najda, Jacek, Mendrek, Wlodzimierz, Sobczyk-Kruszelnicka, Malgorzata, Glowala-Kosinska, Magdalena, Chwieduk, Agata, Mitrus, Iwona, Smagur, Andrzej, Holowiecki, Jerzy, Giebel, Sebastian
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Sprache:eng
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Zusammenfassung:•We provide the first evidence for the advantage of chemomobilization over granulocyte colony-stimulating factor (G-CSF).•An intermediate-dose cytarabine regimen is more efficient in terms of a greater proportion of patients achieving a CD34+ cell yield sufficient for tandem autologous stem cell transplantation (autoSCT), a higher stem cell procurement rate, and faster hematopoietic recovery after autoSCT.•Intermediate-dose cytarabine is superior to G-CSF for patients with multiple myeloma. Mobilization of hematopoietic stem cells for patients with multiple myeloma (MM) may be done using either steady-state granulocyte colony-stimulating factor (G-CSF) or a combination of chemotherapy with G-CSF. The goal of this randomized, open-label, phase 3 trial was to compare the efficacy of chemomobilization using intermediate-dose cytarabine (ID-AraC) plus G-CSF with G-CSF alone in patients with MM referred for tandem autologous stem cell transplantation (autoSCT). The percentage of patients with stem cell yield of at least 5 × 106 CD34+ cells/kg was the primary endpoint. Ninety patients were enrolled, including 44 assigned to the ID-AraC arm and 46 in the G-CSF arm. The threshold number of CD34+ cells was reached in 43 patients (98%) in the ID-AraC arm and in 32 patients (70%) in the G-CSF arm (P = .0003). The median number of collected CD34+ cells was 20.2 × 106 cells/kg in the ID-AraC arm versus 5.9 × 106 cells/kg in the G-CSF arm (P < .000001). A single apheresis was sufficient to achieve the required number of harvested CD34+ cells in 37 patients (86%) in the ID-AraC arm and in 13 patients (41%) in the G-CSF arm (P = .00008). The times to both neutrophil and platelet recovery after autoSCT were significantly shorter in the patients mobilized with ID-AraC. This study provides the first evidence of the advantage of chemomobilization over G-CSF monotherapy in terms of efficacy. ID-AraC with G-CSF should be the preferred chemomobilization protocol for patients with MM scheduled to undergo tandem autoSCT.
ISSN:1083-8791
1523-6536
DOI:10.1016/j.bbmt.2018.09.023