Seminars in Hematology
Volume 46, Supplement 3 , Pages S27-S33, April 2009

New Directions in the Treatment of Imatinib Failure and/or Resistance

  • Francis J. Giles

      Affiliations

    • Corresponding Author InformationAddress correspondence to Francis J. Giles, MD, FRCPI, FRCPath, CTRC at the University of Texas Health Science Center at San Antonio, 7979 Wurzbach Rd, San Antonio, TX 78229

Cancer Therapy and Research Center at the University of Texas Health Science Center at San Antonio, San Antonio, TX

For the minority of chronic myeloid leukemia (CML) patients who demonstrate primary or secondary resistance or intolerance to first-line imatinib therapy, previously available treatment options were limited to cytotoxic chemotherapy, interferon alfa, or allogeneic hematopoietic stem cell transplantation. While the latter option remains a possibility for some, strong clinical efficacy data from recent phase II trials have led to the approval of two second-generation tyrosine kinase inhibitors (TKIs), nilotinib and dasatinib, for the treatment of CML following imatinib failure and/or resistance. Treatment guidelines now recommend either of these two agents as second-line therapy for most patients, although the decision of which second-generation agent to use remains subjective, and is often dependent on the agents' tolerability profiles, as comparative efficacy data from head-to-head clinical studies are not available. Sequential treatment with all three TKIs over the course of the disease is also a possibility, as both nilotinib and dasatinib have shown activity in patients with resistance to imatinib and a subsequent TKI. Novel therapeutic options are continually being developed to expand the range of treatment options, and new tyrosine kinase inhibitors or agents with other mechanisms of action, such as histone deacetylase inhibitors, may prove effective in patients with resistance or intolerance to multiple agents.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

 Editorial support was provided by Jeni Fagan (Health Interactions) on behalf of Novartis Oncology.

 STATEMENT OF CONFLICT OF INTEREST: Dr Giles received research support from Novartis Pharmaceuticals Corp.

PII: S0037-1963(09)00022-5

doi:10.1053/j.seminhematol.2009.01.011

Seminars in Hematology
Volume 46, Supplement 3 , Pages S27-S33, April 2009