Literature DB >> 20685131

The significance of early, major and stable molecular responses in chronic myeloid leukemia in the imatinib era.

Massimo Breccia1, Giuliana Alimena.   

Abstract

Tyrosine kinase inhibitors (TKI) have dramatically changed the management and the outcome of chronic myeloid leukemia (CML) patients. Imatinib is recognized as gold standard first-line therapy and impressive clinical and cytogenetic responses are obtained in the majority of chronic phase patients treated with this drug. Quantitative polymerase chain reaction (RQ-PCR) tool is used to monitor molecular residual disease, but practical issues are associated to measurement of molecular responses. Several evidences have now proved that molecular responses have prognostic significance: patients who achieve early molecular response are more likely to obtain durable cytogenetic response and to present less rate of disease progression. While some reports indicated that achieving major molecular response (MMR) represents the most important endpoint associated to best outcome, some other reports indicated that achievement of MMR does not improve the greatest clinical benefit brought by complete cytogenetic response. In this review, we discuss on the role of molecular monitoring, the significance of early response and its correlation with outcome, the significance of major and complete molecular response, the emphasized value of a stable molecular response, the early identification of resistance presenting with increased molecular level.
Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.

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Year:  2010        PMID: 20685131     DOI: 10.1016/j.critrevonc.2010.07.003

Source DB:  PubMed          Journal:  Crit Rev Oncol Hematol        ISSN: 1040-8428            Impact factor:   6.312


  6 in total

1.  Precision tyrosine kinase inhibitor dosing in chronic myeloid leukemia?

Authors:  Giuseppe Saglio; Carmen Fava; Robert Peter Gale
Journal:  Haematologica       Date:  2019-05       Impact factor: 9.941

Review 2.  Leukemia stem cells: Old concepts and new perspectives.

Authors:  Samanta A Mariani; Bruno Calabretta
Journal:  Mol Aspects Med       Date:  2013-06-29

3.  Genetic basis for the increased expression of vacuolar H+ translocating ATPase genes upon imatinib treatment in human lymphoblastoid cells.

Authors:  Hemant Kulkarni; Harald H H Göring; Joanne E Curran; Vincent Diego; Thomas D Dyer; Shelley Cole; Ken R Walder; Greg R Collier; John Blangero; Melanie A Carless
Journal:  Cancer Chemother Pharmacol       Date:  2013-02-19       Impact factor: 3.333

4.  Sudden blast phase in chronic myeloid leukemia developed during nilotinib therapy after major molecular response was achieved.

Authors:  Yosuke Okada; Ken Sato; Shinichi Kobayashi; Shigeki Nagao; Kosuke Takano; Masahiro Teramoto; Noriaki Tachi; Toshikuni Kawamura; Toshikatsu Horiuchi; Shoichiro Kato; Reina Saga; Takaaki Maekawa; Takeshi Yamamura; Junichi Watanabe; Ayako Kobayashi; Fumihiko Kimura
Journal:  Int J Hematol       Date:  2017-10-14       Impact factor: 2.490

Review 5.  Monitoring the Response to Tyrosine Kinase Inhibitor (TKI) Treatment in Chronic Myeloid Leukemia (CML).

Authors:  Ibrahim C Haznedaroglu
Journal:  Mediterr J Hematol Infect Dis       Date:  2014-01-01       Impact factor: 2.576

Review 6.  Role of tyrosine-kinase inhibitors in myeloproliferative neoplasms: comparative lessons learned.

Authors:  Javier Pinilla-Ibarz; Kendra L Sweet; Gabriela M Corrales-Yepez; Rami S Komrokji
Journal:  Onco Targets Ther       Date:  2016-08-10       Impact factor: 4.147

  6 in total

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