Literature DB >> 15224366

Imatinib mesylate-sensitive blast crisis immediately after discontinuation of imatinib mesylate therapy in chronic myelogenous leukemia: report of two cases.

Takehiro Higashi1, Junichi Tsukada, Chiaki Kato, Atsushi Iwashige, Takamitsu Mizobe, Shinichiro Machida, Hiroaki Morimoto, Ryosuke Ogawa, Yoko Toda, Yoshiya Tanaka.   

Abstract

Although imatinib mesylate has shown encouraging activity in chronic myelogenous leukemia (CML), disease progression during therapy has been observed, manifested by clonal expansion of imatinib mesylate-resistant leukemia cells. On the other hand, myelosuppression related to treatment of imatinib mesylate is often managed with temporary interruption of treatment or dose reduction. We here report two CML patients who had imatinib mesylate-sensitive blast crisis (BC) immediately after discontinuation of imatinib mesylate therapy. The patients discontinued therapy because of neutropenia. Although there was no evidence of blastic phase during therapy, BC occurred 2 weeks after the withdrawal of treatment in both cases. Interestingly, additional chromosomal abnormalities were detected following the withdrawal of imatinib mesylate and disappeared by re-introduction of this agent. The same doses of imatinib mesylate was still effective and remission was sustained with imatinib mesylate alone again. Our report suggests the possibility that withdrawal of imatinib mesylate may lead to proliferation of blast clones even in patients showing good responses to imatinib mesylate without signs of disease progression. Copyright 2004 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15224366     DOI: 10.1002/ajh.20096

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  11 in total

Review 1.  Applying the discovery of the Philadelphia chromosome.

Authors:  Daniel W Sherbenou; Brian J Druker
Journal:  J Clin Invest       Date:  2007-08       Impact factor: 14.808

Review 2.  Sustained complete cytogenetic remission in a patient with chronic myeloid leukemia after discontinuation of imatinib mesylate therapy.

Authors:  Seiichi Okabe; Tetsuzo Tauchi; Yuko Ishii; Daigo Akahane; Kousuke Nunoda; Seiko Honda; Tomoiku Takaku; Kazuma Ohyashiki
Journal:  Int J Hematol       Date:  2007-02       Impact factor: 2.490

3.  BCR-ABL SH3-SH2 domain mutations in chronic myeloid leukemia patients on imatinib.

Authors:  Daniel W Sherbenou; Oliver Hantschel; Ines Kaupe; Stephanie Willis; Thomas Bumm; Lalita P Turaga; Thoralf Lange; Kim-Hien Dao; Richard D Press; Brian J Druker; Giulio Superti-Furga; Michael W Deininger
Journal:  Blood       Date:  2010-06-02       Impact factor: 22.113

4.  Sudden blastic crisis and additional chromosomal abnormalities during chronic myeloid leukemia in the imatinib era.

Authors:  Ridvan Ali; Fahir Ozkalemkas; Vildan Ozkocaman; Tahsin Yakut; Hulya Ozturk Nazlioglu; Ferah Budak; Murat Pekgoz; Serhat Korkmaz; Mutlu Karkucak; Tulay Ozcelik; Ahmet Tunali
Journal:  Int J Clin Oncol       Date:  2009-12-05       Impact factor: 3.402

5.  The CML stem cell: evolution of the progenitor.

Authors:  Scott A Stuart; Yosuke Minami; Jean Y J Wang
Journal:  Cell Cycle       Date:  2009-05-17       Impact factor: 4.534

6.  PML targeting eradicates quiescent leukaemia-initiating cells.

Authors:  Keisuke Ito; Rosa Bernardi; Alessandro Morotti; Sahoko Matsuoka; Giuseppe Saglio; Yasuo Ikeda; Jacalyn Rosenblatt; David E Avigan; Julie Teruya-Feldstein; Pier Paolo Pandolfi
Journal:  Nature       Date:  2008-05-11       Impact factor: 49.962

7.  Effective and selective inhibition of chronic myeloid leukemia primitive hematopoietic progenitors by the dual Src/Abl kinase inhibitor SKI-606.

Authors:  Heiko Konig; Tessa L Holyoake; Ravi Bhatia
Journal:  Blood       Date:  2007-12-04       Impact factor: 22.113

8.  Eradication of chronic myeloid leukemia stem cells: a novel mathematical model predicts no therapeutic benefit of adding G-CSF to imatinib.

Authors:  Jasmine Foo; Mark W Drummond; Bayard Clarkson; Tessa Holyoake; Franziska Michor
Journal:  PLoS Comput Biol       Date:  2009-09-11       Impact factor: 4.475

9.  Effect of cellular quiescence on the success of targeted CML therapy.

Authors:  Natalia L Komarova; Dominik Wodarz
Journal:  PLoS One       Date:  2007-10-03       Impact factor: 3.240

10.  Toward a therapeutic reduction of imatinib refractory myeloproliferative neoplasm-initiating cells.

Authors:  S T Philips; Z L Hildenbrand; K I Oravecz-Wilson; S B Foley; V E Mgbemena; T S Ross
Journal:  Oncogene       Date:  2013-11-18       Impact factor: 9.867

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.