Literature DB >> 18397678

Beyond dose escalation: clinical options for relapse or resistance in chronic myelogenous leukemia.

Jorge Cortes1, Hagop Kantarjian.   

Abstract

The development of imatinib has changed the management of chronic myeloid leukemia (CML), producing high response rates in most patients. However, most individuals treated with imatinib, 400 mg, have residual molecular disease, and both intrinsic and acquired resistance can occur. The newer tyrosine kinase inhibitors, dasatinib and nilotinib, are effective in patients with imatinib-resistant CML, In patients with relapse or resistance, current guidelines recommend escalating the dose of imatinib or switching to new tyrosine kinase inhibitors. Dasatinib has been investigated in patients who were resistant or intolerant to imatinib. Switching to dasatinib, 70 mg, twice daily has been shown to be more effective than high-dose imatinib. Another study found that dasatinib, 100 mg, once daily was just as effective as the twice-daily regimen but was better tolerated. Nilotinib is also effective in most patients with resistance or intolerance to imatinib and is associated with minimal toxicity. Other inhibitors, such as bosutinib and INNO-406, are being developed with favorable early results. New drugs are still needed, particularly for individuals who are resistant to tyrosine kinase inhibitors or those with the T3151 mutation. Emerging CML therapies, some of which have different mechanisms of action from those of tyrosine kinase inhibitors, have shown promising results and could offer an alternative to these patients as monotherapy or in combination.

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Year:  2008        PMID: 18397678

Source DB:  PubMed          Journal:  J Natl Compr Canc Netw        ISSN: 1540-1405            Impact factor:   11.908


  5 in total

1.  Extensive pleural and pericardial effusion in chronic myeloid leukemia during treatment with dasatinib at 100 mg or 50 mg daily.

Authors:  Maria-Theresa Krauth; Susanne Herndlhofer; Maria-Theresa Schmook; Gerlinde Mitterbauer-Hohendanner; Ernst Schlögl; Peter Valent
Journal:  Haematologica       Date:  2010-10-07       Impact factor: 9.941

2.  Results of dasatinib therapy in patients with early chronic-phase chronic myeloid leukemia.

Authors:  Jorge E Cortes; Dan Jones; Susan O'Brien; Elias Jabbour; Farhad Ravandi; Charles Koller; Gautam Borthakur; Brenda Walker; Weiqiang Zhao; Jianqin Shan; Hagop Kantarjian
Journal:  J Clin Oncol       Date:  2009-12-14       Impact factor: 44.544

3.  Nilotinib-induced vasculopathy: identification of vascular endothelial cells as a primary target site.

Authors:  E Hadzijusufovic; K Albrecht-Schgoer; K Huber; G Hoermann; F Grebien; G Eisenwort; W Schgoer; S Herndlhofer; C Kaun; M Theurl; W R Sperr; U Rix; I Sadovnik; B Jilma; G H Schernthaner; J Wojta; D Wolf; G Superti-Furga; R Kirchmair; P Valent
Journal:  Leukemia       Date:  2017-07-31       Impact factor: 11.528

4.  Nilotinib as front-line treatment for patients with chronic myeloid leukemia in early chronic phase.

Authors:  Jorge E Cortes; Dan Jones; Susan O'Brien; Elias Jabbour; Marina Konopleva; Alessandra Ferrajoli; Tapan Kadia; Gautam Borthakur; Denise Stigliano; Jianqin Shan; Hagop Kantarjian
Journal:  J Clin Oncol       Date:  2009-12-14       Impact factor: 44.544

5.  Sensitive detection of pre-existing BCR-ABL kinase domain mutations in CD34+ cells of newly diagnosed chronic-phase chronic myeloid leukemia patients is associated with imatinib resistance: implications in the post-imatinib era.

Authors:  Zafar Iqbal; Aamer Aleem; Mudassar Iqbal; Mubashar Iqbal Naqvi; Ammara Gill; Abid Sohail Taj; Abdul Qayyum; Najeeb ur-Rehman; Ahmad Mukhtar Khalid; Ijaz Hussain Shah; Muhammad Khalid; Riazul Haq; Mahwish Khan; Shahid Mahmood Baig; Abid Jamil; Muhammad Naeem Abbas; Muhammad Absar; Amer Mahmood; Mahmood Rasool; Tanveer Akhtar
Journal:  PLoS One       Date:  2013-02-08       Impact factor: 3.240

  5 in total

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