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PMID: 11801461 Published · ppublish English Evaluation Study Journal Article Research Support, Non-U.S. Gov't

Collection of Philadelphia-negative stem cells using recombinant human granulocyte colony-stimulating factor in chronic myeloid leukemia patients treated with alpha-interferon.

Haematologica ·Vol. 87 ·No. 1 ·2002-01-00 ·Pages 17-22

Hernández-Boluda JC, Carreras E, Cervantes F, Marín P, Arellano-Rodrigo E, Rovira M, Solé F, Lloveras E, Espinet B, Ocejo A, Montserrat E

Abstract

Autologous stem cell transplantation is a therapeutic option for chronic myeloid leukemia (CML) patients who are not candidates for allogeneic transplant. To reduce the risk of post-autografting disease recurrence, different strategies of stem cell selection have been attempted. The results of using recombinant human granulocyte colony-stimulating factor (rHuG-CSF) for harvesting hematopoietic progenitors in CML patients treated with interferon-a (IFN) are reported. Twenty-one CML patients who received IFN for a median of 21 (8-68) months were mobilized with rHuG-CSF (10 mg/kg/day). Twelve were in complete (CCR) or major (MCR) cytogenetic response. Complete success was considered a sufficient harvest (> 1 x 10(6)/kg CD34(+) cells/kg) without Philadelphia (Ph)+ metaphases in at least one apheresis; a partial success was a sufficient harvest with 1-35% Ph(+) cells. A total of 78 aphereses were performed. No patient had major side-effects. The median number (range) of mononuclear and CD34(+) cells obtained was, respectively, 8.6 x 10(8)/kg (0.9-22.6) and 3.3 x 10(6)/kg (0.4-26.3) per patient. A sufficient cell yield was collected in all but three patients. A complete/partial success was achieved in seven CCR/MCR patients (63%) and in three (33%) with other responses. Four patients underwent successful autografting using the stem cells obtained after rHuG-CSF mobilization. Mobilization of IFN-treated patients using rHuG-CSF is safe and provides a significant proportion of Ph-negative progenitors in CML patients in complete or major cytogenetic response.

MeSH Terms
Adolescent Adult Antineoplastic Combined Chemotherapy Protocols/therapeutic use Blood Cell Count Blood Component Removal Bone Marrow Purging/methods,statistics & numerical data Busulfan/administration & dosage,therapeutic use Cytarabine/therapeutic use Feasibility Studies Female Filgrastim Granulocyte Colony-Stimulating Factor/adverse effects,pharmacology Hematopoietic Stem Cell Mobilization/methods Hematopoietic Stem Cell Transplantation/statistics & numerical data Hematopoietic Stem Cells/cytology Humans Hydroxyurea/administration & dosage,therapeutic use Immunologic Factors/therapeutic use Interferons/therapeutic use Leukemia, Myelogenous, Chronic, BCR-ABL Positive/blood,drug therapy,therapy Leukocytosis/chemically induced Male Middle Aged Neoplastic Cells, Circulating Pain/chemically induced Philadelphia Chromosome Recombinant Proteins Remission Induction Safety Transplantation, Autologous Treatment Outcome
Chemicals
Immunologic Factors Recombinant Proteins Cytarabine Granulocyte Colony-Stimulating Factor Interferons Busulfan Filgrastim Hydroxyurea
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Hernández-Boluda Juan-Carlos
BMT Unit, Institute of Hematology and Oncology, Department of Hematology, Hospital del Mar, Villaroel 170, 08036 Barcelona, Spain.
Carreras Enric
Cervantes Francisco
Marín Pedro
Arellano-Rodrigo Eduardo
Rovira Montserrat
Solé Francesc
Lloveras Elisabet
Espinet Blanca
Ocejo Agustín
Montserrat Emili
Article Info
Journal
Haematologica
Abbr.
Haematologica
ISSN
0390-6078
Published
2002-01-00
Pages
17-22
Language
English
Region
Italy
NLM ID
0417435
Subset
IM
Corrections
CommentIn
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