European LeukemiaNet recommendations for the management and avoidance of adverse events of treatment in chronic myeloid leukaemia
Most reports on chronic myeloid leukaemia (CML) treatment with tyrosine kinase inhibitors (TKIs) focus on efficacy, particularly on molecular response and outcome. In contrast, adverse events (AEs) are often reported as infrequent, minor, tolerable and manageable, but they are increasingly important...
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creator | Steegmann, J L Baccarani, M Breccia, M Casado, L F García-Gutiérrez, V Hochhaus, A Kim, D-W Kim, T D Khoury, H J Le Coutre, P Mayer, J Milojkovic, D Porkka, K Rea, D Rosti, G Saussele, S Hehlmann, R Clark, R E |
description | Most reports on chronic myeloid leukaemia (CML) treatment with tyrosine kinase inhibitors (TKIs) focus on efficacy, particularly on molecular response and outcome. In contrast, adverse events (AEs) are often reported as infrequent, minor, tolerable and manageable, but they are increasingly important as therapy is potentially lifelong and multiple TKIs are available. For this reason, the European LeukemiaNet panel for CML management recommendations presents an exhaustive and critical summary of AEs emerging during CML treatment, to assist their understanding, management and prevention. There are five major conclusions. First, the main purpose of CML treatment is the antileukemic effect. Suboptimal management of AEs must not compromise this first objective. Second, most patients will have AEs, usually early, mostly mild to moderate, and which will resolve spontaneously or are easily controlled by simple means. Third, reduction or interruption of treatment must only be done if optimal management of the AE cannot be accomplished in other ways, and frequent monitoring is needed to detect resolution of the AE as early as possible. Fourth, attention must be given to comorbidities and drug interactions, and to new events unrelated to TKIs that are inevitable during such a prolonged treatment. Fifth, some TKI-related AEs have emerged which were not predicted or detected in earlier studies, maybe because of suboptimal attention to or absence from the preclinical data. Overall, imatinib has demonstrated a good long-term safety profile, though recent findings suggest underestimation of symptom severity by physicians. Second and third generation TKIs have shown higher response rates, but have been associated with unexpected problems, some of which could be irreversible. We hope these recommendations will help to minimise adverse events, and we believe that an optimal management of them will be rewarded by better TKI compliance and thus better CML outcomes, together with better quality of life. |
doi_str_mv | 10.1038/leu.2016.104 |
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In contrast, adverse events (AEs) are often reported as infrequent, minor, tolerable and manageable, but they are increasingly important as therapy is potentially lifelong and multiple TKIs are available. For this reason, the European LeukemiaNet panel for CML management recommendations presents an exhaustive and critical summary of AEs emerging during CML treatment, to assist their understanding, management and prevention. There are five major conclusions. First, the main purpose of CML treatment is the antileukemic effect. Suboptimal management of AEs must not compromise this first objective. Second, most patients will have AEs, usually early, mostly mild to moderate, and which will resolve spontaneously or are easily controlled by simple means. Third, reduction or interruption of treatment must only be done if optimal management of the AE cannot be accomplished in other ways, and frequent monitoring is needed to detect resolution of the AE as early as possible. Fourth, attention must be given to comorbidities and drug interactions, and to new events unrelated to TKIs that are inevitable during such a prolonged treatment. Fifth, some TKI-related AEs have emerged which were not predicted or detected in earlier studies, maybe because of suboptimal attention to or absence from the preclinical data. Overall, imatinib has demonstrated a good long-term safety profile, though recent findings suggest underestimation of symptom severity by physicians. Second and third generation TKIs have shown higher response rates, but have been associated with unexpected problems, some of which could be irreversible. We hope these recommendations will help to minimise adverse events, and we believe that an optimal management of them will be rewarded by better TKI compliance and thus better CML outcomes, together with better quality of life.</description><identifier>ISSN: 0887-6924</identifier><identifier>EISSN: 1476-5551</identifier><identifier>DOI: 10.1038/leu.2016.104</identifier><identifier>PMID: 27121688</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/67/1990/283/1896 ; 692/699/1541 ; 692/699/67/1059 ; 692/700/565/2194 ; Cancer ; Cancer Research ; Care and treatment ; Chronic myeloid leukemia ; Complications and side effects ; Correspondence ; Critical Care Medicine ; Drug-Related Side Effects and Adverse Reactions ; Enzyme inhibitors ; Evaluation ; Hematology ; Hospitals ; Humans ; Intensive ; Internal Medicine ; Leukemia ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - complications ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy ; Medicine ; Medicine & Public Health ; Oncology ; Practice guidelines (Medicine) ; Protein Kinase Inhibitors - adverse effects ; Protein Kinase Inhibitors - therapeutic use ; Protein-Tyrosine Kinases - antagonists & inhibitors ; Quality of life ; Review</subject><ispartof>Leukemia, 2016-08, Vol.30 (8), p.1648-1671</ispartof><rights>The Author(s) 2016</rights><rights>COPYRIGHT 2016 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Aug 2016</rights><rights>Copyright © 2016 Macmillan Publishers Limited 2016 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c581t-d9f4001d3b74d438f67cedf70a1d6d4e8d6284ca8a956f71ec7b8955b8e65f6f3</citedby><cites>FETCH-LOGICAL-c581t-d9f4001d3b74d438f67cedf70a1d6d4e8d6284ca8a956f71ec7b8955b8e65f6f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/leu.2016.104$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/leu.2016.104$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27121688$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Steegmann, J L</creatorcontrib><creatorcontrib>Baccarani, M</creatorcontrib><creatorcontrib>Breccia, M</creatorcontrib><creatorcontrib>Casado, L F</creatorcontrib><creatorcontrib>García-Gutiérrez, V</creatorcontrib><creatorcontrib>Hochhaus, A</creatorcontrib><creatorcontrib>Kim, D-W</creatorcontrib><creatorcontrib>Kim, T D</creatorcontrib><creatorcontrib>Khoury, H J</creatorcontrib><creatorcontrib>Le Coutre, P</creatorcontrib><creatorcontrib>Mayer, J</creatorcontrib><creatorcontrib>Milojkovic, D</creatorcontrib><creatorcontrib>Porkka, K</creatorcontrib><creatorcontrib>Rea, D</creatorcontrib><creatorcontrib>Rosti, G</creatorcontrib><creatorcontrib>Saussele, S</creatorcontrib><creatorcontrib>Hehlmann, R</creatorcontrib><creatorcontrib>Clark, R E</creatorcontrib><title>European LeukemiaNet recommendations for the management and avoidance of adverse events of treatment in chronic myeloid leukaemia</title><title>Leukemia</title><addtitle>Leukemia</addtitle><addtitle>Leukemia</addtitle><description>Most reports on chronic myeloid leukaemia (CML) treatment with tyrosine kinase inhibitors (TKIs) focus on efficacy, particularly on molecular response and outcome. In contrast, adverse events (AEs) are often reported as infrequent, minor, tolerable and manageable, but they are increasingly important as therapy is potentially lifelong and multiple TKIs are available. For this reason, the European LeukemiaNet panel for CML management recommendations presents an exhaustive and critical summary of AEs emerging during CML treatment, to assist their understanding, management and prevention. There are five major conclusions. First, the main purpose of CML treatment is the antileukemic effect. Suboptimal management of AEs must not compromise this first objective. Second, most patients will have AEs, usually early, mostly mild to moderate, and which will resolve spontaneously or are easily controlled by simple means. Third, reduction or interruption of treatment must only be done if optimal management of the AE cannot be accomplished in other ways, and frequent monitoring is needed to detect resolution of the AE as early as possible. Fourth, attention must be given to comorbidities and drug interactions, and to new events unrelated to TKIs that are inevitable during such a prolonged treatment. Fifth, some TKI-related AEs have emerged which were not predicted or detected in earlier studies, maybe because of suboptimal attention to or absence from the preclinical data. Overall, imatinib has demonstrated a good long-term safety profile, though recent findings suggest underestimation of symptom severity by physicians. Second and third generation TKIs have shown higher response rates, but have been associated with unexpected problems, some of which could be irreversible. We hope these recommendations will help to minimise adverse events, and we believe that an optimal management of them will be rewarded by better TKI compliance and thus better CML outcomes, together with better quality of life.</description><subject>631/67/1990/283/1896</subject><subject>692/699/1541</subject><subject>692/699/67/1059</subject><subject>692/700/565/2194</subject><subject>Cancer</subject><subject>Cancer Research</subject><subject>Care and treatment</subject><subject>Chronic myeloid leukemia</subject><subject>Complications and side effects</subject><subject>Correspondence</subject><subject>Critical Care Medicine</subject><subject>Drug-Related Side Effects and Adverse Reactions</subject><subject>Enzyme inhibitors</subject><subject>Evaluation</subject><subject>Hematology</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Intensive</subject><subject>Internal Medicine</subject><subject>Leukemia</subject><subject>Leukemia, Myelogenous, Chronic, BCR-ABL Positive - complications</subject><subject>Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Oncology</subject><subject>Practice guidelines (Medicine)</subject><subject>Protein Kinase Inhibitors - adverse effects</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Protein-Tyrosine Kinases - antagonists & inhibitors</subject><subject>Quality of 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LeukemiaNet recommendations for the management and avoidance of adverse events of treatment in chronic myeloid leukaemia</title><author>Steegmann, J L ; Baccarani, M ; Breccia, M ; Casado, L F ; García-Gutiérrez, V ; Hochhaus, A ; Kim, D-W ; Kim, T D ; Khoury, H J ; Le Coutre, P ; Mayer, J ; Milojkovic, D ; Porkka, K ; Rea, D ; Rosti, G ; Saussele, S ; Hehlmann, R ; Clark, R E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c581t-d9f4001d3b74d438f67cedf70a1d6d4e8d6284ca8a956f71ec7b8955b8e65f6f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>631/67/1990/283/1896</topic><topic>692/699/1541</topic><topic>692/699/67/1059</topic><topic>692/700/565/2194</topic><topic>Cancer</topic><topic>Cancer Research</topic><topic>Care and treatment</topic><topic>Chronic myeloid leukemia</topic><topic>Complications and side effects</topic><topic>Correspondence</topic><topic>Critical Care 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M</au><au>Breccia, M</au><au>Casado, L F</au><au>García-Gutiérrez, V</au><au>Hochhaus, A</au><au>Kim, D-W</au><au>Kim, T D</au><au>Khoury, H J</au><au>Le Coutre, P</au><au>Mayer, J</au><au>Milojkovic, D</au><au>Porkka, K</au><au>Rea, D</au><au>Rosti, G</au><au>Saussele, S</au><au>Hehlmann, R</au><au>Clark, R E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>European LeukemiaNet recommendations for the management and avoidance of adverse events of treatment in chronic myeloid leukaemia</atitle><jtitle>Leukemia</jtitle><stitle>Leukemia</stitle><addtitle>Leukemia</addtitle><date>2016-08-01</date><risdate>2016</risdate><volume>30</volume><issue>8</issue><spage>1648</spage><epage>1671</epage><pages>1648-1671</pages><issn>0887-6924</issn><eissn>1476-5551</eissn><abstract>Most reports on chronic myeloid leukaemia (CML) treatment with tyrosine kinase inhibitors (TKIs) focus on efficacy, particularly on molecular response and outcome. In contrast, adverse events (AEs) are often reported as infrequent, minor, tolerable and manageable, but they are increasingly important as therapy is potentially lifelong and multiple TKIs are available. For this reason, the European LeukemiaNet panel for CML management recommendations presents an exhaustive and critical summary of AEs emerging during CML treatment, to assist their understanding, management and prevention. There are five major conclusions. First, the main purpose of CML treatment is the antileukemic effect. Suboptimal management of AEs must not compromise this first objective. Second, most patients will have AEs, usually early, mostly mild to moderate, and which will resolve spontaneously or are easily controlled by simple means. Third, reduction or interruption of treatment must only be done if optimal management of the AE cannot be accomplished in other ways, and frequent monitoring is needed to detect resolution of the AE as early as possible. Fourth, attention must be given to comorbidities and drug interactions, and to new events unrelated to TKIs that are inevitable during such a prolonged treatment. Fifth, some TKI-related AEs have emerged which were not predicted or detected in earlier studies, maybe because of suboptimal attention to or absence from the preclinical data. Overall, imatinib has demonstrated a good long-term safety profile, though recent findings suggest underestimation of symptom severity by physicians. Second and third generation TKIs have shown higher response rates, but have been associated with unexpected problems, some of which could be irreversible. We hope these recommendations will help to minimise adverse events, and we believe that an optimal management of them will be rewarded by better TKI compliance and thus better CML outcomes, together with better quality of life.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>27121688</pmid><doi>10.1038/leu.2016.104</doi><tpages>24</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/67/1990/283/1896 692/699/1541 692/699/67/1059 692/700/565/2194 Cancer Cancer Research Care and treatment Chronic myeloid leukemia Complications and side effects Correspondence Critical Care Medicine Drug-Related Side Effects and Adverse Reactions Enzyme inhibitors Evaluation Hematology Hospitals Humans Intensive Internal Medicine Leukemia Leukemia, Myelogenous, Chronic, BCR-ABL Positive - complications Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy Medicine Medicine & Public Health Oncology Practice guidelines (Medicine) Protein Kinase Inhibitors - adverse effects Protein Kinase Inhibitors - therapeutic use Protein-Tyrosine Kinases - antagonists & inhibitors Quality of life Review |
title | European LeukemiaNet recommendations for the management and avoidance of adverse events of treatment in chronic myeloid leukaemia |
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