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Nilotinib is effective in patients with chronic myeloid leukemia in chronic phase after imatinib resistance or intolerance: 24-month follow-up results

  • Hagop M. Kantarjian
  • , Francis J. Giles
  • , Kapil N. Bhalla
  • , Javier Pinilla-Ibarz
  • , Richard A. Larson
  • , Norbert Gattermann
  • , Oliver G. Ottmann
  • , Andreas Hochhaus
  • , Jerald P. Radich
  • , Giuseppe Saglio
  • , Timothy P. Hughes
  • , Giovanni Martinelli
  • , Dong Wook Kim
  • , Yaping Shou
  • , Neil J. Gallagher
  • , Rick Blakesley
  • , Michele Baccarani
  • , Jorge Cortes
  • , Philipp D. Le Coutre
  • The University of Texas Health Science Center at Houston
  • Institute for Drug Development
  • Georgia Regents University
  • Moffitt Cancer Center
  • University of Chicago
  • Heinrich-Heine-University
  • Goethe University
  • Jena University Hospital
  • Fred Hutchinson Cancer Center
  • University of Turin
  • Royal Adelaide Hospital
  • University of Bologna
  • Department of Internal Medicine
  • Novartis Institutes for Biomedical Research
  • Novartis Institutes for Biomedical Research
  • Charité – Universitätsmedizin Berlin

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

334 Citations (Scopus)

Abstract

Nilotinib is a potent selective inhibitor of the BCR-ABL tyrosine kinase approved for use in patients with newly diagnosed chronic myeloid leukemia in chronic phase (CML-CP), and in CML-CP and CML-accelerated phase after imatinib failure. Nilotinib (400 mg twice daily) was approved on the basis of the initial results of this phase 2 open-label study. The primary study endpoint was the proportion of patients achieving major cytogenetic response (CyR). All patients were followed for ≥ 24 months or discontinued early. Of 321 patients, 124 (39%) continue on nilotinib treatment. Overall, 59% of patients achieved major CyR; this was completeCyR (CCyR) in 44%. Of patients achieving CCyR, 56% achieved major molecular response. CyRs were durable, with 84% of patients who achieved CCyR maintaining response at 24 months. The overall survival at 24 months was 87%. Adverse events were mostly mild to moderate, generally transient, and easily managed. This study indicates that nilotinib is effective, with a manageable safety profile, and can provide favorable long-term benefits for patients with CML-CP after imatinib failure. This trial was registered at www.clinicaltrials.gov as #NCT00109707.

Original languageEnglish
Pages (from-to)1141-1145
Number of pages5
JournalBlood
Volume117
Issue number4
DOIs
Publication statusPublished - 27 Jan 2011
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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