BASAK, Grzegorz W., Ozren JAKSIC, Zdeněk KOŘÍSTEK, Gabor MIKALA, Sandra BASIC-KINDA, Jiří MAYER, Tamas MASSZI, Sebastian GIEBEL, Boris LABAR a Wieslaw WIKTOR-JEDRZEJCZAK. Haematopoietic stem cell mobilization with plerixafor and G-CSF in patients with multiple myeloma transplanted with autologous stem cells. European Journal of Haematology. 2011, roč. 86, č. 6, s. 488-495. ISSN 0902-4441. Dostupné z: https://dx.doi.org/10.1111/j.1600-0609.2011.01605.x.
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Základní údaje
Originální název Haematopoietic stem cell mobilization with plerixafor and G-CSF in patients with multiple myeloma transplanted with autologous stem cells
Autoři BASAK, Grzegorz W. (616 Polsko, garant), Ozren JAKSIC (191 Chorvatsko), Zdeněk KOŘÍSTEK (203 Česká republika, domácí), Gabor MIKALA (348 Maďarsko), Sandra BASIC-KINDA (191 Chorvatsko), Jiří MAYER (203 Česká republika, domácí), Tamas MASSZI (348 Maďarsko), Sebastian GIEBEL (616 Polsko), Boris LABAR (191 Chorvatsko) a Wieslaw WIKTOR-JEDRZEJCZAK (616 Polsko).
Vydání European Journal of Haematology, 2011, 0902-4441.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30200 3.2 Clinical medicine
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 2.614
Kód RIV RIV/00216224:14110/11:00055087
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1111/j.1600-0609.2011.01605.x
UT WoS 000290731000005
Klíčová slova anglicky plerixafor; stem cell mobilization; myeloma; autologous stem cell transplantation
Příznaky Mezinárodní význam
Změnil Změnil: Mgr. Michal Petr, učo 65024. Změněno: 23. 1. 2012 13:27.
Anotace
A proportion of patients with multiple myeloma (MM) who have already undergone autologous stem cell transplantation (autoSCT) might benefit from a further transplantation. For this, they might need to undergo another round of stem cell mobilization. We analyzed retrospectively the outcomes of stem cell mobilization with plerixafor and granulocyte colony-stimulating factor (G-CSF) in a group of 30 patients who had undergone autoSCT previously, and in 46 other patients. The previously transplanted patients were significantly different from the remaining patients with respect to the intensity and number of previous therapies. We observed that the median peripheral blood concentration of CD34+ cells after the first administration of plerixafor was lower in previously transplanted (19 cells/mu L) than in other patients (30 cells/mu L). Despite a comparable number of apheresis sessions being performed, the median total yield of CD34+ cells was significantly lower in the previously transplanted than in the remaining patients (2.8 x 106 cells/kg vs. 4.2 x 106 cells/kg). However, successful collection of at least 2.0 x 106 CD34+ cells/kg was achieved finally in a similar proportion of previously transplanted and other patients (70% vs. 82.6%). Our data suggest that stem cell mobilization with plerixafor and G-CSF might overcome the negative effect of prognostic factors for poor stem cell mobilization in patients with MM who have undergone autoSCT previously.
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