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      Non ABL-directed inhibitors as alternative treatment strategies for chronic myeloid leukemia

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          Abstract

          The introduction of ABL Tyrosine Kinase Inhibitors (TKIs) has significantly improved the outcome of Chronic Myeloid Leukemia (CML) patients that, in large part, achieve satisfactory hematological, cytogenetic and molecular remissions. However, approximately 15–20% fail to obtain optimal responses according to the current European Leukemia Network recommendation because of drug intolerance or resistance.

          Moreover, a plethora of evidence suggests that Leukemic Stem Cells (LSCs) show BCR-ABL1-independent survival. Hence, they are unresponsive to TKIs, leading to disease relapse if pharmacological treatment is discontinued.

          All together, these biological events generate a subpopulation of CML patients in need of alternative therapeutic strategies to overcome TKI resistance or to eradicate LSCs in order to allow cure of the disease.

          In this review we update the role of “ non ABL-directed inhibitors” targeting signaling pathways downstream of the BCR-ABL1 oncoprotein and describe immunological approaches activating specific T cell responses against CML cells.

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          Most cited references118

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          European LeukemiaNet recommendations for the management of chronic myeloid leukemia: 2013.

          Advances in chronic myeloid leukemia treatment, particularly regarding tyrosine kinase inhibitors, mandate regular updating of concepts and management. A European LeukemiaNet expert panel reviewed prior and new studies to update recommendations made in 2009. We recommend as initial treatment imatinib, nilotinib, or dasatinib. Response is assessed with standardized real quantitative polymerase chain reaction and/or cytogenetics at 3, 6, and 12 months. BCR-ABL1 transcript levels ≤10% at 3 months, 10% at 6 months and >1% from 12 months onward define failure, mandating a change in treatment. Similarly, partial cytogenetic response (PCyR) at 3 months and complete cytogenetic response (CCyR) from 6 months onward define optimal response, whereas no CyR (Philadelphia chromosome-positive [Ph+] >95%) at 3 months, less than PCyR at 6 months, and less than CCyR from 12 months onward define failure. Between optimal and failure, there is an intermediate warning zone requiring more frequent monitoring. Similar definitions are provided for response to second-line therapy. Specific recommendations are made for patients in the accelerated and blastic phases, and for allogeneic stem cell transplantation. Optimal responders should continue therapy indefinitely, with careful surveillance, or they can be enrolled in controlled studies of treatment discontinuation once a deeper molecular response is achieved.
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            The HSP90 chaperone machinery

            The heat shock protein 90 (HSP90) chaperone machinery is a key regulator of proteostasis. Recent progress has shed light on the interactions of HSP90 with its clients and co-chaperones, and on their functional implications. This opens up new avenues for the development of drugs that target HSP90, which could be valuable for the treatment of cancers and protein-misfolding diseases.
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              Letter: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining.

              J D Rowley (1973)
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                Author and article information

                Contributors
                +39 095 3781950 , pvigneri@libero.it
                Journal
                Mol Cancer
                Mol. Cancer
                Molecular Cancer
                BioMed Central (London )
                1476-4598
                19 February 2018
                19 February 2018
                2018
                : 17
                : 56
                Affiliations
                [1 ]ISNI 0000 0004 1757 1969, GRID grid.8158.4, Department of Clinical and Experimental Medicine, , University of Catania, ; Via Santa Sofia, 78, Catania, 95123 Italy
                [2 ]Center of Experimental Oncology and Hematology, A.O.U. Policlinico Vittorio Emanuele, Via Santa Sofia, 78, 95123 Catania, Italy
                [3 ]ISNI 0000 0004 1757 1969, GRID grid.8158.4, Department of Surgical Medical Sciences and Advanced Technologies, , University of Catania, ; Via Santa Sofia, 78, Catania, 95123 Italy
                [4 ]ISNI 0000 0004 1757 1969, GRID grid.8158.4, Division of Hematology and Bone Marrow Transplant, , University of Catania, ; Via Santa Sofia, 78, Catania, 95123 Italy
                [5 ]ISNI 0000 0004 1757 1969, GRID grid.8158.4, Department of Surgery, Medical and Surgical Specialties, , University of Catania, ; Via Santa Sofia, 78, Catania, 95123 Italy
                Author information
                http://orcid.org/0000-0002-5943-6066
                Article
                805
                10.1186/s12943-018-0805-1
                5817805
                29455672
                ab056d91-c29b-48a3-8fa5-1e8a6275901a
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 26 October 2017
                : 1 February 2018
                Funding
                Funded by: AIRC
                Award ID: IG12958
                Award Recipient :
                Categories
                Review
                Custom metadata
                © The Author(s) 2018

                Oncology & Radiotherapy
                cml,bcr-abl1,therapeutic strategies,immunological approaches
                Oncology & Radiotherapy
                cml, bcr-abl1, therapeutic strategies, immunological approaches

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