Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2011 Feb;52(2):209-17.
doi: 10.1007/s00108-010-2782-3.

[Modern therapy of chronic myeloid leukemia: an example for paradigma shift in hemato-oncology]

[Article in German]
Affiliations

[Modern therapy of chronic myeloid leukemia: an example for paradigma shift in hemato-oncology]

[Article in German]
A A Leitner et al. Internist (Berl). 2011 Feb.

Erratum in

  • Internist (Berl). 2011 May;52(5):517

Abstract

Chronic myeloid leukemia (CML) is exceptional amongst neoplasias since its underlying pathomechanism has been elucidated, and potent well tolerated targeted drugs, the tyrosine kinase inhibitors (TKI), are available for treatment. They convincingly improve prognosis while retaining good quality of life. Aims of therapy are complete remissions as well as prolongation of life and cure. Imatinib 400 mg per day is current standard therapy. There are hints for a better outcome with a higher initial imatinib dose or with combination therapy. Even after achievement of complete molecular response continuous therapy might be necessary in most cases. In case of imatinib intolerance or failure, the second generation TKI dasatinib and nilotinib and allogeneic stem cell transplantation are available. The use of second generation TKI as first line treatment might further improve prognosis. The therapeutic response should be regularly monitored according to international recommendations.

PubMed Disclaimer

References

    1. Leukemia. 2003 Aug;17(8):1529-37 - PubMed
    1. N Engl J Med. 2006 Dec 7;355(23):2408-17 - PubMed
    1. Nature. 2009 Apr 16;458(7240):904-8 - PubMed
    1. Blood. 2010 Mar 11;115(10):1880-5 - PubMed
    1. Cancer Res. 1996 Jan 1;56(1):100-4 - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources