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NCCN Task Force report: tyrosine kinase inhibitor therapy selection in the management of patients with chronic myelogenous leukemia.

Publication ,  Journal Article
O'Brien, S; Berman, E; Moore, JO; Pinilla-Ibarz, J; Radich, JP; Shami, PJ; Smith, BD; Snyder, DS; Sundar, HM; Talpaz, M; Wetzler, M
Published in: J Natl Compr Canc Netw
February 2011

The advent of imatinib has dramatically improved outcomes in patients with chronic myelogenous leukemia (CML). It has become the standard of care for all patients with newly diagnosed chronic-phase CML based on its successful induction of durable responses in most patients. However, its use is complicated by the development of resistance in some patients. Dose escalation might overcome this resistance if detected early. The second-generation tyrosine kinase inhibitors (TKIs) dasatinib and nilotinib provide effective therapeutic options for managing patients resistant or intolerant to imatinib. Recent studies have shown that dasatinib and nilotinib provide quicker and potentially better responses than standard-dose imatinib when used as a first-line treatment. The goal of therapy for patients with CML is the achievement of a complete cytogenetic response, and eventually a major molecular response, to prevent disease progression to accelerated or blast phase. Selecting the appropriate TKI depends on many factors, including disease phase, primary or secondary resistance to TKI, the agent's side effect profile and its relative effectiveness against BCR-ABL mutations, and the patient's tolerance to therapy. In October 2010, NCCN organized a task force consisting of a panel of experts from NCCN Member Institutions with expertise in the management of patients with CML to discuss these issues. This report provides recommendations regarding the selection of TKI therapy for the management of patients with CML based on the evaluation of available published clinical data and expert opinion among the task force members.

Duke Scholars

Published In

J Natl Compr Canc Netw

DOI

EISSN

1540-1413

Publication Date

February 2011

Volume

9 Suppl 2

Issue

0 2

Start / End Page

S1 / 25

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Protein Kinase Inhibitors
  • Oncology & Carcinogenesis
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive
  • Humans
  • Drug Resistance, Neoplasm
  • Disease Progression
  • Clinical Trials as Topic
  • 4203 Health services and systems
  • 3211 Oncology and carcinogenesis
 

Citation

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MLA
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O’Brien, S., Berman, E., Moore, J. O., Pinilla-Ibarz, J., Radich, J. P., Shami, P. J., … Wetzler, M. (2011). NCCN Task Force report: tyrosine kinase inhibitor therapy selection in the management of patients with chronic myelogenous leukemia. J Natl Compr Canc Netw, 9 Suppl 2(0 2), S1-25. https://doi.org/10.6004/jnccn.2011.0125
O’Brien, Susan, Ellin Berman, Joseph O. Moore, Javier Pinilla-Ibarz, Jerald P. Radich, Paul J. Shami, B Douglas Smith, et al. “NCCN Task Force report: tyrosine kinase inhibitor therapy selection in the management of patients with chronic myelogenous leukemia.J Natl Compr Canc Netw 9 Suppl 2, no. 0 2 (February 2011): S1-25. https://doi.org/10.6004/jnccn.2011.0125.
O’Brien S, Berman E, Moore JO, Pinilla-Ibarz J, Radich JP, Shami PJ, et al. NCCN Task Force report: tyrosine kinase inhibitor therapy selection in the management of patients with chronic myelogenous leukemia. J Natl Compr Canc Netw. 2011 Feb;9 Suppl 2(0 2):S1-25.
O’Brien, Susan, et al. “NCCN Task Force report: tyrosine kinase inhibitor therapy selection in the management of patients with chronic myelogenous leukemia.J Natl Compr Canc Netw, vol. 9 Suppl 2, no. 0 2, Feb. 2011, pp. S1-25. Pubmed, doi:10.6004/jnccn.2011.0125.
O’Brien S, Berman E, Moore JO, Pinilla-Ibarz J, Radich JP, Shami PJ, Smith BD, Snyder DS, Sundar HM, Talpaz M, Wetzler M. NCCN Task Force report: tyrosine kinase inhibitor therapy selection in the management of patients with chronic myelogenous leukemia. J Natl Compr Canc Netw. 2011 Feb;9 Suppl 2(0 2):S1-25.

Published In

J Natl Compr Canc Netw

DOI

EISSN

1540-1413

Publication Date

February 2011

Volume

9 Suppl 2

Issue

0 2

Start / End Page

S1 / 25

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Protein Kinase Inhibitors
  • Oncology & Carcinogenesis
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive
  • Humans
  • Drug Resistance, Neoplasm
  • Disease Progression
  • Clinical Trials as Topic
  • 4203 Health services and systems
  • 3211 Oncology and carcinogenesis