POOR HEMOPOIETIC STEM CELL MOBILIZERS IN MULTIPLE MYELOMA : A SINGLE INSTITUTION EXPERIENCE
Author(s) -
Guillermo J. RuizDelgado,
Avril López-Otero,
Ana Hernández-Arizpe,
Aura Ramirez-Medina,
Guillermo J. RuízArgüelles
Publication year - 2010
Publication title -
mediterranean journal of hematology and infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.682
H-Index - 31
ISSN - 2035-3006
DOI - 10.4084/mjhid.2010.016
Subject(s) - cd34 , medicine , multiple myeloma , apheresis , stem cell , haematopoiesis , autologous stem cell transplantation , plerixafor , filgrastim , oncology , immunology , chemotherapy , granulocyte colony stimulating factor , cxcr4 , platelet , biology , microbiology and biotechnology , chemokine , receptor
In a single institution, in a group of 28 myeloma patients deemed eligible for autologous transplant, stem cell mobilization was attempted using filgrastim: 26 individuals were given 31 autografts employing 1–4 (median three) apheresis sessions, to obtain a target stem cell dose of 1 x 10 6 CD34 +ve viable cells / Kg of the recipient. The median number of grafted CD34 cells was 7.56 x 10 6 / Kg of the recipient; the range being 0.92 to 14.8. By defining as poor mobilizers individuals in which a cell collection of < 1 x 10 6 CD34 viable cells / Kg was obtained, a subset of eight poor mobilizers was identified; in two patients the autograft was aborted because of an extremely poor CD34 +ve cell yield (< 0.2 x 10 6 CD34 +ve viable cells / Kg of the recipient) after four apheresis sessions. The long-term overall survival of the patients grafted with > 1 x 10 6 CD34 +ve viable cells / Kg was better (80% at 80 months) than those grafted with < 1 x 10 6 CD34 +ve viable cells / Kg (67% at 76 months). Methods to improve stem cell mobilization are needed and may result in obtaining better results when autografting multiple myeloma patients.
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