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Minimal Residual Disease Assessment and Risk-based Therapy in Acute Lymphoblastic Leukemia
The study of minimal residual disease (MRD) in adult patients with acute lymphoblastic leukemia (ALL) allows a greater refinement of the individual risk classification and is the best support for risk-specific therapy with or without allogeneic hematopoietic cell transplantation (HCT). Using case-sp...
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Published in: | Clinical lymphoma, myeloma and leukemia myeloma and leukemia, 2017-07, Vol.17, p.S2-S9 |
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creator | Bassan, Renato Intermesoli, Tamara Scattolin, Annamaria Viero, Piera Maino, Elena Sancetta, Rosaria Carobolante, Francesca Gianni, Francesca Stefanoni, Paola Tosi, Manuela Spinelli, Orietta Rambaldi, Alessandro |
description | The study of minimal residual disease (MRD) in adult patients with acute lymphoblastic leukemia (ALL) allows a greater refinement of the individual risk classification and is the best support for risk-specific therapy with or without allogeneic hematopoietic cell transplantation (HCT). Using case-specific sensitive molecular probes or multiparametric flow cytometry on marrow samples obtained from the end of induction until midconsolidation, MRD assays can detect up to 1 leukemic cell of 10,000 total mononuclear cells (sensitivity, 0.01%; ie, ≥104). This cutoff, presently bound to technical limitations and subject to improvement, reflects the individual chemosensitivity and is strongly correlated with treatment outcome. The chance for cure is approximately 70% in the MRD-negative subset but only 20% to 30% in MRD-positive patients, in any diagnostic and risk subset. As shown by prospective trials from Germany, Italy, Spain, and France-Switzerland-Belgium, approximately 50% to 70% of unselected adult patients with Philadelphia-negative ALL achieve and maintain an early MRD response, whereas the remainder do not, including a substantial proportion of clinically standard-risk patients, and require an HCT to avert at least partially the risk of relapse. Along with the diffusion of more effective “pediatric-inspired” chemotherapy programs, the MRD analysis is an integral part of a modern management strategy, guiding the decision process to transplant or not, in which case nonrelapse mortality using HCT in first remission—still 10% to 20%—is totally abolished. The use of new agents such as monoclonal antibodies, small inhibitors, and chimeric antigen receptor T cells is opening a new era of MRD-directed therapies, that will further increase survival rates. |
doi_str_mv | 10.1016/j.clml.2017.02.019 |
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Using case-specific sensitive molecular probes or multiparametric flow cytometry on marrow samples obtained from the end of induction until midconsolidation, MRD assays can detect up to 1 leukemic cell of 10,000 total mononuclear cells (sensitivity, 0.01%; ie, ≥104). This cutoff, presently bound to technical limitations and subject to improvement, reflects the individual chemosensitivity and is strongly correlated with treatment outcome. The chance for cure is approximately 70% in the MRD-negative subset but only 20% to 30% in MRD-positive patients, in any diagnostic and risk subset. As shown by prospective trials from Germany, Italy, Spain, and France-Switzerland-Belgium, approximately 50% to 70% of unselected adult patients with Philadelphia-negative ALL achieve and maintain an early MRD response, whereas the remainder do not, including a substantial proportion of clinically standard-risk patients, and require an HCT to avert at least partially the risk of relapse. Along with the diffusion of more effective “pediatric-inspired” chemotherapy programs, the MRD analysis is an integral part of a modern management strategy, guiding the decision process to transplant or not, in which case nonrelapse mortality using HCT in first remission—still 10% to 20%—is totally abolished. The use of new agents such as monoclonal antibodies, small inhibitors, and chimeric antigen receptor T cells is opening a new era of MRD-directed therapies, that will further increase survival rates.</description><identifier>ISSN: 2152-2650</identifier><identifier>EISSN: 2152-2669</identifier><identifier>DOI: 10.1016/j.clml.2017.02.019</identifier><identifier>PMID: 28760298</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; ALL ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Child ; Disease-Free Survival ; Hematopoietic Stem Cell Transplantation - methods ; Humans ; Management ; MRD ; Neoplasm, Residual - diagnosis ; Outcome Assessment (Health Care) - methods ; Outcome Assessment (Health Care) - statistics & numerical data ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy ; Prognosis ; Risk classification ; Risk Factors</subject><ispartof>Clinical lymphoma, myeloma and leukemia, 2017-07, Vol.17, p.S2-S9</ispartof><rights>2017 Elsevier Inc.</rights><rights>Copyright © 2017 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-a95328a2dc0854b7c3fa6bbbbb205d46770666446408e20774639ffabf4195483</citedby><cites>FETCH-LOGICAL-c356t-a95328a2dc0854b7c3fa6bbbbb205d46770666446408e20774639ffabf4195483</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28760298$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bassan, Renato</creatorcontrib><creatorcontrib>Intermesoli, Tamara</creatorcontrib><creatorcontrib>Scattolin, Annamaria</creatorcontrib><creatorcontrib>Viero, Piera</creatorcontrib><creatorcontrib>Maino, Elena</creatorcontrib><creatorcontrib>Sancetta, Rosaria</creatorcontrib><creatorcontrib>Carobolante, Francesca</creatorcontrib><creatorcontrib>Gianni, Francesca</creatorcontrib><creatorcontrib>Stefanoni, Paola</creatorcontrib><creatorcontrib>Tosi, Manuela</creatorcontrib><creatorcontrib>Spinelli, Orietta</creatorcontrib><creatorcontrib>Rambaldi, Alessandro</creatorcontrib><title>Minimal Residual Disease Assessment and Risk-based Therapy in Acute Lymphoblastic Leukemia</title><title>Clinical lymphoma, myeloma and leukemia</title><addtitle>Clin Lymphoma Myeloma Leuk</addtitle><description>The study of minimal residual disease (MRD) in adult patients with acute lymphoblastic leukemia (ALL) allows a greater refinement of the individual risk classification and is the best support for risk-specific therapy with or without allogeneic hematopoietic cell transplantation (HCT). 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Along with the diffusion of more effective “pediatric-inspired” chemotherapy programs, the MRD analysis is an integral part of a modern management strategy, guiding the decision process to transplant or not, in which case nonrelapse mortality using HCT in first remission—still 10% to 20%—is totally abolished. The use of new agents such as monoclonal antibodies, small inhibitors, and chimeric antigen receptor T cells is opening a new era of MRD-directed therapies, that will further increase survival rates.</description><subject>Adult</subject><subject>ALL</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Child</subject><subject>Disease-Free Survival</subject><subject>Hematopoietic Stem Cell Transplantation - methods</subject><subject>Humans</subject><subject>Management</subject><subject>MRD</subject><subject>Neoplasm, Residual - diagnosis</subject><subject>Outcome Assessment (Health Care) - methods</subject><subject>Outcome Assessment (Health Care) - statistics & numerical data</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy</subject><subject>Prognosis</subject><subject>Risk classification</subject><subject>Risk Factors</subject><issn>2152-2650</issn><issn>2152-2669</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kE1P3DAQhq2qqFDoH-ih8pFL0rHjj0TisoJCKy1CQnDpxXKcifCSjyWTVNp_j1cLHDuXGWmeeaV5GPsuIBcgzM9NHrq-yyUIm4PMQVSf2IkUWmbSmOrzx6zhmH0l2gBYSNAXdixLa0BW5Qn7exuH2PuO3yPFZknDVST0hHxFhEQ9DjP3Q8PvIz1ndVo0_OEJJ7_d8TjwVVhm5Otdv30a687THANf4_KMffRn7Kj1HeG3t37KHq9_PVz-ztZ3N38uV-ssFNrMma90IUsvmwClVrUNRetNvS8JulHGWjDGKGUUlCjBWmWKqm193SpRaVUWp-z8kLudxpcFaXZ9pIBd5wccF3KiklpaqYVKqDygYRqJJmzddkrfTzsnwO2duo3bO3V7pw6kS7rS0Y-3_KXusfk4eZeYgIsDgOnLfxEnRyHiELCJE4bZNWP8X_4ri6SHVA</recordid><startdate>201707</startdate><enddate>201707</enddate><creator>Bassan, Renato</creator><creator>Intermesoli, Tamara</creator><creator>Scattolin, Annamaria</creator><creator>Viero, Piera</creator><creator>Maino, Elena</creator><creator>Sancetta, Rosaria</creator><creator>Carobolante, Francesca</creator><creator>Gianni, Francesca</creator><creator>Stefanoni, Paola</creator><creator>Tosi, Manuela</creator><creator>Spinelli, Orietta</creator><creator>Rambaldi, Alessandro</creator><general>Elsevier Inc</general><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>7X8</scope></search><sort><creationdate>201707</creationdate><title>Minimal Residual Disease Assessment and Risk-based Therapy in Acute Lymphoblastic Leukemia</title><author>Bassan, Renato ; Intermesoli, Tamara ; Scattolin, Annamaria ; Viero, Piera ; Maino, Elena ; Sancetta, Rosaria ; Carobolante, Francesca ; Gianni, Francesca ; Stefanoni, Paola ; Tosi, Manuela ; Spinelli, Orietta ; Rambaldi, Alessandro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-a95328a2dc0854b7c3fa6bbbbb205d46770666446408e20774639ffabf4195483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>ALL</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Child</topic><topic>Disease-Free Survival</topic><topic>Hematopoietic Stem Cell Transplantation - methods</topic><topic>Humans</topic><topic>Management</topic><topic>MRD</topic><topic>Neoplasm, Residual - diagnosis</topic><topic>Outcome Assessment (Health Care) - methods</topic><topic>Outcome Assessment (Health Care) - statistics & numerical data</topic><topic>Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy</topic><topic>Prognosis</topic><topic>Risk classification</topic><topic>Risk Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bassan, Renato</creatorcontrib><creatorcontrib>Intermesoli, Tamara</creatorcontrib><creatorcontrib>Scattolin, Annamaria</creatorcontrib><creatorcontrib>Viero, Piera</creatorcontrib><creatorcontrib>Maino, Elena</creatorcontrib><creatorcontrib>Sancetta, Rosaria</creatorcontrib><creatorcontrib>Carobolante, Francesca</creatorcontrib><creatorcontrib>Gianni, Francesca</creatorcontrib><creatorcontrib>Stefanoni, Paola</creatorcontrib><creatorcontrib>Tosi, Manuela</creatorcontrib><creatorcontrib>Spinelli, Orietta</creatorcontrib><creatorcontrib>Rambaldi, Alessandro</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical lymphoma, myeloma and leukemia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bassan, Renato</au><au>Intermesoli, Tamara</au><au>Scattolin, Annamaria</au><au>Viero, Piera</au><au>Maino, Elena</au><au>Sancetta, Rosaria</au><au>Carobolante, Francesca</au><au>Gianni, Francesca</au><au>Stefanoni, Paola</au><au>Tosi, Manuela</au><au>Spinelli, Orietta</au><au>Rambaldi, Alessandro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Minimal Residual Disease Assessment and Risk-based Therapy in Acute Lymphoblastic Leukemia</atitle><jtitle>Clinical lymphoma, myeloma and leukemia</jtitle><addtitle>Clin Lymphoma Myeloma Leuk</addtitle><date>2017-07</date><risdate>2017</risdate><volume>17</volume><spage>S2</spage><epage>S9</epage><pages>S2-S9</pages><issn>2152-2650</issn><eissn>2152-2669</eissn><abstract>The study of minimal residual disease (MRD) in adult patients with acute lymphoblastic leukemia (ALL) allows a greater refinement of the individual risk classification and is the best support for risk-specific therapy with or without allogeneic hematopoietic cell transplantation (HCT). Using case-specific sensitive molecular probes or multiparametric flow cytometry on marrow samples obtained from the end of induction until midconsolidation, MRD assays can detect up to 1 leukemic cell of 10,000 total mononuclear cells (sensitivity, 0.01%; ie, ≥104). This cutoff, presently bound to technical limitations and subject to improvement, reflects the individual chemosensitivity and is strongly correlated with treatment outcome. The chance for cure is approximately 70% in the MRD-negative subset but only 20% to 30% in MRD-positive patients, in any diagnostic and risk subset. As shown by prospective trials from Germany, Italy, Spain, and France-Switzerland-Belgium, approximately 50% to 70% of unselected adult patients with Philadelphia-negative ALL achieve and maintain an early MRD response, whereas the remainder do not, including a substantial proportion of clinically standard-risk patients, and require an HCT to avert at least partially the risk of relapse. Along with the diffusion of more effective “pediatric-inspired” chemotherapy programs, the MRD analysis is an integral part of a modern management strategy, guiding the decision process to transplant or not, in which case nonrelapse mortality using HCT in first remission—still 10% to 20%—is totally abolished. The use of new agents such as monoclonal antibodies, small inhibitors, and chimeric antigen receptor T cells is opening a new era of MRD-directed therapies, that will further increase survival rates.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28760298</pmid><doi>10.1016/j.clml.2017.02.019</doi></addata></record> |
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subjects | Adult ALL Antineoplastic Combined Chemotherapy Protocols - therapeutic use Child Disease-Free Survival Hematopoietic Stem Cell Transplantation - methods Humans Management MRD Neoplasm, Residual - diagnosis Outcome Assessment (Health Care) - methods Outcome Assessment (Health Care) - statistics & numerical data Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy Prognosis Risk classification Risk Factors |
title | Minimal Residual Disease Assessment and Risk-based Therapy in Acute Lymphoblastic Leukemia |
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