| Literature DB >> 19481800 |
Massimo Breccia1, Francesca Palandri, Anna Paola Iori, Elisabetta Colaci, Roberto Latagliata, Fausto Castagnetti, Giovanni Fernando Torelli, Sara Usai, Veronica Valle, Giovanni Martinelli, Gianantonio Rosti, Robin Foà, Michele Baccarani, Giuliana Alimena.
Abstract
Philadelphia-positive chronic myeloid leukemia (Ph+ CML) patients who are resistant to imatinib are commonly treated with second-generation tyrosine kinase inhibitors (TKIs). Limited data exist on the possible effects of these drugs on subsequent allogeneic hematopoietic stem cell transplantation (allo-HSCT).The outcome of 12 imatinib-resistant CML patients treated with dasatinib or nilotinib or both before allo-HSCT, was retrospectively analyzed. Patients were treated with second-generation TKIs for 1-17 months (median, 8). At the time of transplant, 3 patients were in complete cytogenetic response (CCgR), 3 patients in partial cytogenetic response (PCgR) and 6 patients were in less than PCgR. Donors were HLA-matched related in 4 cases and unrelated in 8 cases. Stem cell source was peripheral blood, bone marrow or cord blood in 6, 5 and 1 cases, respectively. All patients engrafted successfully and all but one achieved a full donor chimerism. Three patients experienced acute and chronic graft-versus-host disease. No cases of transplant-related mortality were recorded. Best response to allo-HSCT was complete molecular response (CMR) in 9 patients, major molecular response (MMR) in 1 patient and CCgR in 2 patients. Median follow-up was 16.5 months. At the last evaluation, 9 patients were in continuous CMR and 1 patient was in MMR; 2 patients had died of disease progression. Second-generation TKIs given before allo-HSCT do not negatively affect transplant engraftment and response rate, nor increases transplant-related toxicity. Copyright 2009 Elsevier Ltd. All rights reserved.Entities:
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Year: 2009 PMID: 19481800 DOI: 10.1016/j.leukres.2009.04.036
Source DB: PubMed Journal: Leuk Res ISSN: 0145-2126 Impact factor: 3.156