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Br J Haematol ; 132(1): 42-55, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16371019

ABSTRACT

We investigated the feasibility, safety and efficacy of two B-cell purging methods in patients with CD20+ non-Hodgkin lymphoma (NHL) receiving autologous stsem cell transplantation. Myeloid and immune recoveries between the methods were compared. Twenty-seven patients were randomised to either in vivo purging with rituximab or ex vivo purging by CD34+ cell selection. Both purging methods were efficient at eliminating B-cells in infusates. When compared with in vivo purging, ex vivo purging was associated with CD34+ cell loss and delayed median neutrophil (10 d vs. 11 d) and platelet (12.5 d vs. 17 d) count recoveries. Lymphocyte recovery was similar in both groups, but immunoglobulin recovery was delayed after in vivo purging. Late-infectious complications were few in both arms. At a median follow-up of 27 months, 2-year probabilities of event-free survival (EFS) rates were 81% for in vivo purging and 76% for ex vivo purging (P = 0.66). When compared with 53 unpurged patients, all 27 purged patients had improved 3-year probabilities of overall survival (89% vs. 70%, P = 0.014) and a trend for improved EFS (78% vs. 57%, P = 0.075). In conclusion, although both purging methods were feasible and safe, rituximab purging was superior as it did not impair CD34+ cell mobilisation and was associated with faster myeloid recovery. Further studies are needed to determine whether rituximab purging is more effective than the use of unpurged autografts.


Subject(s)
Antibodies, Monoclonal/therapeutic use , Antineoplastic Agents/therapeutic use , Bone Marrow Purging/methods , Lymphoma, B-Cell/therapy , Peripheral Blood Stem Cell Transplantation/methods , Adult , Aged , Antibodies, Monoclonal, Murine-Derived , Antigens, CD34/analysis , Feasibility Studies , Female , Hematopoietic Stem Cell Mobilization/methods , Humans , Immunomagnetic Separation/methods , Leukapheresis/methods , Lymphoma, B-Cell/drug therapy , Male , Middle Aged , Rituximab
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