Making Treatment-Free Remission (TFR) Easier in Chronic Myeloid Leukemia: Fact-Checking and Practical Management Tools
In chronic-phase chronic myeloid leukemia (CML), tyrosine kinase inhibitors (TKIs) are the standard of care, and treatment-free remission (TFR) following the achievement of a stable deep molecular response (DMR) has become, alongside survival, a primary goal for virtually all patients. The GIMEMA CM...
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creator | Castagnetti, Fausto Binotto, Gianni Capodanno, Isabella Billio, Atto Calistri, Elisabetta Cavazzini, Francesco Crugnola, Monica Gozzini, Antonella Gugliotta, Gabriele Krampera, Mauro Lucchesi, Alessandro Merli, Anna Miggiano, Maria Cristina Minotto, Claudia Poggiaspalla, Monica Salvucci, Marzia Scappini, Barbara Tiribelli, Mario Trabacchi, Elena Rosti, Gianantonio Galimberti, Sara Bonifacio, Massimiliano |
description | In chronic-phase chronic myeloid leukemia (CML), tyrosine kinase inhibitors (TKIs) are the standard of care, and treatment-free remission (TFR) following the achievement of a stable deep molecular response (DMR) has become, alongside survival, a primary goal for virtually all patients. The GIMEMA CML working party recently suggested that the possibility of achieving TFR cannot be denied to any patient, and proposed specific treatment policies according to the patient’s age and risk. However, other international recommendations (including 2020 ELN recommendations) are more focused on survival and provide less detailed suggestions on how to choose first and subsequent lines of treatment. Consequently, some grey areas remain. After literature review, a panel of Italian experts discussed the following controversial issues: (1)
early prediction of DMR and TFR
: female sex, non-high disease risk score, e14a2 transcript and early MR achievement have been associated with stable DMR, but the lack of these criteria is not sufficient to exclude any patient from TFR; (2)
criteria for first and subsequent line therapy choice
: a number of patient and drug characteristics have been proposed to make a personalized decision; (3)
monitoring of residual disease after discontinuation
: after the first 6 months, the frequency of molecular tests can be reduced based on MR4.5 persistence and short turnaround time; (4)
prognosis of TFR
: therapy and DMR duration are important to predict TFR; although immunological control of CML plays a role, no immunological predictive phenotype is currently available. This guidance is intended as a practical tool to support physicians in decision making. |
doi_str_mv | 10.1007/s11523-021-00831-4 |
format | Article |
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early prediction of DMR and TFR
: female sex, non-high disease risk score, e14a2 transcript and early MR achievement have been associated with stable DMR, but the lack of these criteria is not sufficient to exclude any patient from TFR; (2)
criteria for first and subsequent line therapy choice
: a number of patient and drug characteristics have been proposed to make a personalized decision; (3)
monitoring of residual disease after discontinuation
: after the first 6 months, the frequency of molecular tests can be reduced based on MR4.5 persistence and short turnaround time; (4)
prognosis of TFR
: therapy and DMR duration are important to predict TFR; although immunological control of CML plays a role, no immunological predictive phenotype is currently available. This guidance is intended as a practical tool to support physicians in decision making.</description><identifier>ISSN: 1776-2596</identifier><identifier>EISSN: 1776-260X</identifier><identifier>DOI: 10.1007/s11523-021-00831-4</identifier><identifier>PMID: 34661826</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Biomedicine ; Female ; Humans ; Immunology ; Leukemia ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - genetics ; Medical prognosis ; Medicine ; Medicine & Public Health ; Oncology ; Prognosis ; Protein Kinase Inhibitors - therapeutic use ; Remission (Medicine) ; Remission Induction ; Therapy in Practice ; Treatment Outcome</subject><ispartof>Targeted oncology, 2021-11, Vol.16 (6), p.823-838</ispartof><rights>The Author(s) 2021</rights><rights>2021. The Author(s).</rights><rights>The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-10c201104b1ccf08c4d0ad4e4d34af666d0fe3a254fd6d6d513319a23d476aef3</citedby><cites>FETCH-LOGICAL-c474t-10c201104b1ccf08c4d0ad4e4d34af666d0fe3a254fd6d6d513319a23d476aef3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11523-021-00831-4$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11523-021-00831-4$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34661826$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Castagnetti, Fausto</creatorcontrib><creatorcontrib>Binotto, Gianni</creatorcontrib><creatorcontrib>Capodanno, Isabella</creatorcontrib><creatorcontrib>Billio, Atto</creatorcontrib><creatorcontrib>Calistri, Elisabetta</creatorcontrib><creatorcontrib>Cavazzini, Francesco</creatorcontrib><creatorcontrib>Crugnola, Monica</creatorcontrib><creatorcontrib>Gozzini, Antonella</creatorcontrib><creatorcontrib>Gugliotta, Gabriele</creatorcontrib><creatorcontrib>Krampera, Mauro</creatorcontrib><creatorcontrib>Lucchesi, Alessandro</creatorcontrib><creatorcontrib>Merli, Anna</creatorcontrib><creatorcontrib>Miggiano, Maria Cristina</creatorcontrib><creatorcontrib>Minotto, Claudia</creatorcontrib><creatorcontrib>Poggiaspalla, Monica</creatorcontrib><creatorcontrib>Salvucci, Marzia</creatorcontrib><creatorcontrib>Scappini, Barbara</creatorcontrib><creatorcontrib>Tiribelli, Mario</creatorcontrib><creatorcontrib>Trabacchi, Elena</creatorcontrib><creatorcontrib>Rosti, Gianantonio</creatorcontrib><creatorcontrib>Galimberti, Sara</creatorcontrib><creatorcontrib>Bonifacio, Massimiliano</creatorcontrib><title>Making Treatment-Free Remission (TFR) Easier in Chronic Myeloid Leukemia: Fact-Checking and Practical Management Tools</title><title>Targeted oncology</title><addtitle>Targ Oncol</addtitle><addtitle>Target Oncol</addtitle><description>In chronic-phase chronic myeloid leukemia (CML), tyrosine kinase inhibitors (TKIs) are the standard of care, and treatment-free remission (TFR) following the achievement of a stable deep molecular response (DMR) has become, alongside survival, a primary goal for virtually all patients. The GIMEMA CML working party recently suggested that the possibility of achieving TFR cannot be denied to any patient, and proposed specific treatment policies according to the patient’s age and risk. However, other international recommendations (including 2020 ELN recommendations) are more focused on survival and provide less detailed suggestions on how to choose first and subsequent lines of treatment. Consequently, some grey areas remain. After literature review, a panel of Italian experts discussed the following controversial issues: (1)
early prediction of DMR and TFR
: female sex, non-high disease risk score, e14a2 transcript and early MR achievement have been associated with stable DMR, but the lack of these criteria is not sufficient to exclude any patient from TFR; (2)
criteria for first and subsequent line therapy choice
: a number of patient and drug characteristics have been proposed to make a personalized decision; (3)
monitoring of residual disease after discontinuation
: after the first 6 months, the frequency of molecular tests can be reduced based on MR4.5 persistence and short turnaround time; (4)
prognosis of TFR
: therapy and DMR duration are important to predict TFR; although immunological control of CML plays a role, no immunological predictive phenotype is currently available. This guidance is intended as a practical tool to support physicians in decision making.</description><subject>Biomedicine</subject><subject>Female</subject><subject>Humans</subject><subject>Immunology</subject><subject>Leukemia</subject><subject>Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy</subject><subject>Leukemia, Myelogenous, Chronic, BCR-ABL Positive - genetics</subject><subject>Medical prognosis</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Oncology</subject><subject>Prognosis</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Remission (Medicine)</subject><subject>Remission Induction</subject><subject>Therapy in Practice</subject><subject>Treatment Outcome</subject><issn>1776-2596</issn><issn>1776-260X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kU1vFDEMhkcIRD_gD3BAkbiUQ8D5mMyUAxJadQFpV6BqkbhFbsazm3Y2KclMpf77pt22fBxQDo7ix29sv1X1SsA7AdC8z0LUUnGQggO0SnD9pNoXTWO4NPDz6cO9PjZ71UHO5wC6kTU8r_aUNka00uxXV0u88GHNVolw3FIY-TwRsVPa-px9DOxoNT99y04we0rMBzbbpBi8Y8trGqLv2IKmiwLjBzZHN_LZhtydIIaOfU_lyTsc2BIDrulWn61iHPKL6lmPQ6aX9_Gw-jE_Wc2-8MW3z19nnxbc6UaPXICTIAToM-FcD63THWCnSXdKY2-M6aAnhbLWfWfKqYVS4hil6nRjkHp1WH3c6V5OZ1vqXGkg4WAvk99iurYRvf07E_zGruOVbY1Q0LRF4OheIMVfE-XRlsU4GgYMFKdsZd0qBUZKVdA3_6DncUqhjGeLH6JRBlpTKLmjXIo5J-ofmxFgb221O1ttsdXe2Wp1KXr95xiPJQ8-FkDtgFxSYU3p99__kb0BnaKt_A</recordid><startdate>20211101</startdate><enddate>20211101</enddate><creator>Castagnetti, Fausto</creator><creator>Binotto, Gianni</creator><creator>Capodanno, Isabella</creator><creator>Billio, Atto</creator><creator>Calistri, Elisabetta</creator><creator>Cavazzini, Francesco</creator><creator>Crugnola, Monica</creator><creator>Gozzini, Antonella</creator><creator>Gugliotta, Gabriele</creator><creator>Krampera, Mauro</creator><creator>Lucchesi, Alessandro</creator><creator>Merli, Anna</creator><creator>Miggiano, Maria Cristina</creator><creator>Minotto, Claudia</creator><creator>Poggiaspalla, Monica</creator><creator>Salvucci, Marzia</creator><creator>Scappini, Barbara</creator><creator>Tiribelli, Mario</creator><creator>Trabacchi, Elena</creator><creator>Rosti, Gianantonio</creator><creator>Galimberti, Sara</creator><creator>Bonifacio, Massimiliano</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20211101</creationdate><title>Making Treatment-Free Remission (TFR) Easier in Chronic Myeloid Leukemia: Fact-Checking and Practical Management Tools</title><author>Castagnetti, Fausto ; Binotto, Gianni ; Capodanno, Isabella ; Billio, Atto ; Calistri, Elisabetta ; Cavazzini, Francesco ; Crugnola, Monica ; Gozzini, Antonella ; Gugliotta, Gabriele ; Krampera, Mauro ; Lucchesi, Alessandro ; Merli, Anna ; Miggiano, Maria Cristina ; Minotto, Claudia ; Poggiaspalla, Monica ; Salvucci, Marzia ; Scappini, Barbara ; Tiribelli, Mario ; Trabacchi, Elena ; Rosti, Gianantonio ; Galimberti, Sara ; Bonifacio, Massimiliano</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-10c201104b1ccf08c4d0ad4e4d34af666d0fe3a254fd6d6d513319a23d476aef3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Biomedicine</topic><topic>Female</topic><topic>Humans</topic><topic>Immunology</topic><topic>Leukemia</topic><topic>Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy</topic><topic>Leukemia, Myelogenous, Chronic, BCR-ABL Positive - genetics</topic><topic>Medical prognosis</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Oncology</topic><topic>Prognosis</topic><topic>Protein Kinase Inhibitors - therapeutic use</topic><topic>Remission (Medicine)</topic><topic>Remission Induction</topic><topic>Therapy in Practice</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Castagnetti, Fausto</creatorcontrib><creatorcontrib>Binotto, Gianni</creatorcontrib><creatorcontrib>Capodanno, Isabella</creatorcontrib><creatorcontrib>Billio, Atto</creatorcontrib><creatorcontrib>Calistri, Elisabetta</creatorcontrib><creatorcontrib>Cavazzini, Francesco</creatorcontrib><creatorcontrib>Crugnola, Monica</creatorcontrib><creatorcontrib>Gozzini, Antonella</creatorcontrib><creatorcontrib>Gugliotta, Gabriele</creatorcontrib><creatorcontrib>Krampera, Mauro</creatorcontrib><creatorcontrib>Lucchesi, Alessandro</creatorcontrib><creatorcontrib>Merli, Anna</creatorcontrib><creatorcontrib>Miggiano, Maria Cristina</creatorcontrib><creatorcontrib>Minotto, Claudia</creatorcontrib><creatorcontrib>Poggiaspalla, Monica</creatorcontrib><creatorcontrib>Salvucci, Marzia</creatorcontrib><creatorcontrib>Scappini, Barbara</creatorcontrib><creatorcontrib>Tiribelli, Mario</creatorcontrib><creatorcontrib>Trabacchi, Elena</creatorcontrib><creatorcontrib>Rosti, Gianantonio</creatorcontrib><creatorcontrib>Galimberti, Sara</creatorcontrib><creatorcontrib>Bonifacio, Massimiliano</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Targeted oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Castagnetti, Fausto</au><au>Binotto, Gianni</au><au>Capodanno, Isabella</au><au>Billio, Atto</au><au>Calistri, Elisabetta</au><au>Cavazzini, Francesco</au><au>Crugnola, Monica</au><au>Gozzini, Antonella</au><au>Gugliotta, Gabriele</au><au>Krampera, Mauro</au><au>Lucchesi, Alessandro</au><au>Merli, Anna</au><au>Miggiano, Maria Cristina</au><au>Minotto, Claudia</au><au>Poggiaspalla, Monica</au><au>Salvucci, Marzia</au><au>Scappini, Barbara</au><au>Tiribelli, Mario</au><au>Trabacchi, Elena</au><au>Rosti, Gianantonio</au><au>Galimberti, Sara</au><au>Bonifacio, Massimiliano</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Making Treatment-Free Remission (TFR) Easier in Chronic Myeloid Leukemia: Fact-Checking and Practical Management Tools</atitle><jtitle>Targeted oncology</jtitle><stitle>Targ Oncol</stitle><addtitle>Target Oncol</addtitle><date>2021-11-01</date><risdate>2021</risdate><volume>16</volume><issue>6</issue><spage>823</spage><epage>838</epage><pages>823-838</pages><issn>1776-2596</issn><eissn>1776-260X</eissn><abstract>In chronic-phase chronic myeloid leukemia (CML), tyrosine kinase inhibitors (TKIs) are the standard of care, and treatment-free remission (TFR) following the achievement of a stable deep molecular response (DMR) has become, alongside survival, a primary goal for virtually all patients. The GIMEMA CML working party recently suggested that the possibility of achieving TFR cannot be denied to any patient, and proposed specific treatment policies according to the patient’s age and risk. However, other international recommendations (including 2020 ELN recommendations) are more focused on survival and provide less detailed suggestions on how to choose first and subsequent lines of treatment. Consequently, some grey areas remain. After literature review, a panel of Italian experts discussed the following controversial issues: (1)
early prediction of DMR and TFR
: female sex, non-high disease risk score, e14a2 transcript and early MR achievement have been associated with stable DMR, but the lack of these criteria is not sufficient to exclude any patient from TFR; (2)
criteria for first and subsequent line therapy choice
: a number of patient and drug characteristics have been proposed to make a personalized decision; (3)
monitoring of residual disease after discontinuation
: after the first 6 months, the frequency of molecular tests can be reduced based on MR4.5 persistence and short turnaround time; (4)
prognosis of TFR
: therapy and DMR duration are important to predict TFR; although immunological control of CML plays a role, no immunological predictive phenotype is currently available. This guidance is intended as a practical tool to support physicians in decision making.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>34661826</pmid><doi>10.1007/s11523-021-00831-4</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biomedicine Female Humans Immunology Leukemia Leukemia, Myelogenous, Chronic, BCR-ABL Positive - drug therapy Leukemia, Myelogenous, Chronic, BCR-ABL Positive - genetics Medical prognosis Medicine Medicine & Public Health Oncology Prognosis Protein Kinase Inhibitors - therapeutic use Remission (Medicine) Remission Induction Therapy in Practice Treatment Outcome |
title | Making Treatment-Free Remission (TFR) Easier in Chronic Myeloid Leukemia: Fact-Checking and Practical Management Tools |
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