Tyrosine kinase inhibitors in Ph+ acute lymphoblastic leukaemia: facts and perspectives
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  • 作者:Michele Malagola ; Cristina Papayannidis ; Michele Baccarani
  • 关键词:Acute lymphoblastic leukaemia ; Philadelphia chromosome ; Tyrosine kinase inhibitors ; Target therapy
  • 刊名:Annals of Hematology
  • 出版年:2016
  • 出版时间:April 2016
  • 年:2016
  • 卷:95
  • 期:5
  • 页码:681-693
  • 全文大小:390 KB
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  • 作者单位:Michele Malagola (1) (2)
    Cristina Papayannidis (3)
    Michele Baccarani (4)

    1. Unit of Blood Diseases and Stem Cell Transplantation, AO Spedali Civili di Brescia, Brescia, Italy
    2. Department of Medical and Surgical Sciences, University of Brescia, Brescia, Italy
    3. Department of Specialistic, Diagnostic and Experimental Medicine, S.Orsola-Malpighi University Hospital, University of Bologna, Bologna, Italy
    4. Department of Hematology/Oncology “L. and A. Seràgnoli”, S. Orsola-Malpighi University Hospital, University of Bologna, Bologna, Italy
  • 刊物类别:Medicine
  • 刊物主题:Medicine & Public Health
    Hematology
    Oncology
  • 出版者:Springer Berlin / Heidelberg
  • ISSN:1432-0584
文摘
Two tyrosine kinase inhibitors (TKIs), imatinib and dasatinib, are registered for the treatment of Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukaemia (ALL) in adults. Other two TKIs (nilotinib and ponatinib) have been tested in the second-line, can offer an alternative in the patients who fail the first-line, and can acquire a role also in the first-line. Here, we provide a summary of the reports of TKIs, used alone, and in combination with chemotherapy. TKIs are very effective alone and with corticosteroids and are likely to improve substantially the outcome when they are combined with standard or dose-adapted chemotherapy. While the complete haematologic remission rate is always very high, close to 100 %, the cytogenetic and molecular remission rates are lower, so that TKIs are still considered as a complement to chemotherapy and as a bridge to allogeneic stem cell transplantation (allo-SCT). However, many patients relapse before transplant, and many patients still relapse, even if they have been submitted to allo-SCT. A proper use of TKIs, the introduction of ponatinib, and of “new generation” TKIs should improve further on the outcome of Ph+ ALL.

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