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Nilotinib in imatinib-resistant or imatinib-intolerant patients with chronic myeloid leukemia in chronic phase: 48-month follow-up results of a phase II study

  • F. J. Giles(corresponding author)
    ,
  • P. D. Le Coutre
    ,
  • J. Pinilla-Ibarz
    ,
  • R. A. Larson
    ,
  • N. Gattermann
    ,
  • O. G. Ottmann
*Corresponding author for this work
  • University of Galway
    ,
  • Humboldt University of Berlin
    ,
  • University of South Florida
    ,
  • The University of Chicago
    ,
  • Heinrich Heine University Düsseldorf
    ,
  • Goethe University Frankfurt
Scholary Output:
Contribution to journal
Article
Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Nilotinib (Tasigna) is a BCR-ABL1 tyrosine kinase inhibitor approved for the treatment of patients with Philadelphia chromosome-positive chronic myeloid leukemia in chronic phase (CML-CP) who are newly diagnosed or intolerant of or resistant to imatinib. The 48-month follow-up data for patients with CML-CP treated with nilotinib after imatinib resistance or intolerance on an international phase II study were analyzed. Overall, 59% of patients achieved major cytogenetic response; 45% achieved complete cytogenetic response while on study. The estimated rate of overall survival (OS) and progression-free survival (PFS) at 48 months was 78% and 57%, respectively. Deeper levels of molecular responses at 3 and 6 months were highly positively correlated with long-term outcomes, including PFS and OS at 48 months. Of the 321 patients initially enrolled in the study, 98 (31%) were treated for at least 48 months. Discontinuations were primarily due to disease progression (30%) or adverse events (21%). Nilotinib is safe and effective for long-term use in responding patients with CML-CP who are intolerant of or resistant to imatinib. Further significant improvements in therapy are required for patients who are resistant or intolerant to imatinib.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 107-112 (6 pages)

Journal (Volume, Issue Number)

Leukemia (Volume 27, Issue 1)

Publication milestones

  • Published - 01/2013

Publication status

Published - 01/2013

ISSN

0887-6924

Publication IDs

  • Scopus: 84873568081
  • PubMed: 22763385
  • ORCID: /0000-0002-8636-1071/work/68811020

Publication metrics

Metrics

Fractional count
1
Fractional count
0.06
Fractional count
17
Fractional count
0.94
Fractional count
1
Fractional count
1
Scopus
citations
SciVal
citations
155
SciVal
FWCI
6.96
SciVal
Author count
18
SciVal
Paper percentile
99
SciVal
Top percentile
1

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Citation count
215
Mentions
1
Captures
157

Funding Details

We thank Susan Branford, Philipp Erben, Neil Gallagher, Ariful Haque, Martin Müller and Simona Soverini for their contributions. Financial support for medical editorial assistance was provided by Novartis Pharmaceuticals. We thank Cornel Phillip and Erinn Goldman for medical editorial assistance with this manuscript. The research work of Francis Giles, Philipp D le Coutre, 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, Jorge Cortes, Michele Baccarani and Hagop M Kantarjian was funded by Novartis Pharma.
FundersFunding number
Francis Giles
-
Philipp D le Coutre
-
NCI
P30CA016672
Novartis Pharma
-