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Hematopoietic stem cell transplantation in the era of tyrosine kinase inhibitors.

Abstract
Until the 1990 s, the treatment of chronic myeloid leukemia (CML) recognized hematopoietic stem cell transplantation as the best treatment for those patients with an available donor. With the advent of imatinib in 2001, this paradigm changed dramatically as this drug provided outstanding and durable rates of hematologic, cytogenetic, and molecular responses. As a consequence it became the gold standard first-line treatment for most patients. However, after almost a decade of its use, it is clear that although very effective, imatinib cannot cure CML as transplantation has already proven so. Furthermore, the new non-myeloablative regimens and the improvements in survival after allogeneic transplant, especially in the field of unrelated transplants, offer this option to a broader population of patients with CML. This adds to the old question of whom to transplant, when and how to proceed with the allograft. This article reviews the current role of transplantation in the era of tyrosine kinase inhibitors and will try to elucidate its role in the frontline setting as well as after first- and second-line kinase inhibitors failure.
AuthorsCarlos A Doti, Eduardo O Bullorsky
JournalLeukemia & lymphoma (Leuk Lymphoma) Vol. 50 Suppl 2 Pg. 27-31 (Dec 2009) ISSN: 1029-2403 [Electronic] United States
PMID20017608 (Publication Type: Evaluation Study, Journal Article, Review)
Chemical References
  • Antineoplastic Agents
  • Benzamides
  • Piperazines
  • Protein Kinase Inhibitors
  • Pyrimidines
  • Imatinib Mesylate
  • Protein-Tyrosine Kinases
Topics
  • Antineoplastic Agents (therapeutic use)
  • Benzamides
  • Combined Modality Therapy
  • Drug Resistance, Neoplasm (physiology)
  • Health Planning Guidelines
  • Hematopoietic Stem Cell Transplantation (methods, trends)
  • Humans
  • Imatinib Mesylate
  • Neoadjuvant Therapy
  • Piperazines (therapeutic use)
  • Protein Kinase Inhibitors (therapeutic use)
  • Protein-Tyrosine Kinases (antagonists & inhibitors)
  • Pyrimidines (therapeutic use)

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