Standardized MRD quantification in European ALL trials: Proceedings of the Second International Symposium on MRD assessment in Kiel, Germany, 18-20 September 2008
Assessment of minimal residual disease (MRD) has acquired a prominent position in European treatment protocols for patients with acute lymphoblastic leukemia (ALL), on the basis of its high prognostic value for predicting outcome and the possibilities for implementation of MRD diagnostics in treatme...
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creator | Brüggemann, M Schrauder, A Raff, T Pfeifer, H Dworzak, M Ottmann, O G Asnafi, V Baruchel, A Bassan, R Benoit, Y Biondi, A Cavé, H Dombret, H Fielding, A K Foà, R Gökbuget, N Goldstone, A H Goulden, N Henze, G Hoelzer, D Janka-Schaub, G E Macintyre, E A Pieters, R Rambaldi, A Ribera, J-M Schmiegelow, K Spinelli, O Stary, J von Stackelberg, A Kneba, M Schrappe, M van Dongen, J J M |
description | Assessment of minimal residual disease (MRD) has acquired a prominent position in European treatment protocols for patients with acute lymphoblastic leukemia (ALL), on the basis of its high prognostic value for predicting outcome and the possibilities for implementation of MRD diagnostics in treatment stratification. Therefore, there is an increasing need for standardization of methodologies and harmonization of terminology. For this purpose, a panel of representatives of all major European study groups on childhood and adult ALL and of international experts on PCR- and flow cytometry-based MRD assessment was built in the context of the Second International Symposium on MRD assessment in Kiel, Germany, 18–20 September 2008. The panel summarized the current state of MRD diagnostics in ALL and developed recommendations on the minimal technical requirements that should be fulfilled before implementation of MRD diagnostics into clinical trials. Finally, a common terminology for a standard description of MRD response and monitoring was established defining the terms ‘complete MRD response’, ‘MRD persistence’ and ‘MRD reappearance’. The proposed MRD terminology may allow a refined and standardized assessment of response to treatment in adult and childhood ALL, and provides a sound basis for the comparison of MRD results between different treatment protocols. |
doi_str_mv | 10.1038/leu.2009.268 |
format | Article |
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Therefore, there is an increasing need for standardization of methodologies and harmonization of terminology. For this purpose, a panel of representatives of all major European study groups on childhood and adult ALL and of international experts on PCR- and flow cytometry-based MRD assessment was built in the context of the Second International Symposium on MRD assessment in Kiel, Germany, 18–20 September 2008. The panel summarized the current state of MRD diagnostics in ALL and developed recommendations on the minimal technical requirements that should be fulfilled before implementation of MRD diagnostics into clinical trials. Finally, a common terminology for a standard description of MRD response and monitoring was established defining the terms ‘complete MRD response’, ‘MRD persistence’ and ‘MRD reappearance’. The proposed MRD terminology may allow a refined and standardized assessment of response to treatment in adult and childhood ALL, and provides a sound basis for the comparison of MRD results between different treatment protocols.</description><identifier>ISSN: 0887-6924</identifier><identifier>EISSN: 1476-5551</identifier><identifier>DOI: 10.1038/leu.2009.268</identifier><identifier>PMID: 20033054</identifier><identifier>CODEN: LEUKED</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Acute lymphoblastic leukemia ; Acute lymphocytic leukemia ; Biological and medical sciences ; Cancer ; Cancer Research ; Care and treatment ; Children ; Clinical trials ; College campuses ; Critical Care Medicine ; Flow Cytometry ; Fusion Proteins, bcr-abl - genetics ; Gene Rearrangement ; Genes, Immunoglobulin ; Genetic aspects ; Health services ; Hematologic and hematopoietic diseases ; Hematology ; Hospitals ; Humans ; Intensive ; Internal Medicine ; Jargon ; Leukemia ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Lymphatic leukemia ; Medical sciences ; Medicine ; Medicine & Public Health ; Minimal residual disease ; Neoplasm, Residual - diagnosis ; Oncology ; Patient outcomes ; Pediatrics ; Polymerase Chain Reaction ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy ; Relapse ; review ; Standardization ; Terminology</subject><ispartof>Leukemia, 2010-03, Vol.24 (3), p.521-535</ispartof><rights>Macmillan Publishers Limited 2010</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2010 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Mar 2010</rights><rights>Macmillan Publishers Limited 2010.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c672t-78263f0661fd7e0a830206af4a67fc75636cf4ac566e3587737a217284173a543</citedby><cites>FETCH-LOGICAL-c672t-78263f0661fd7e0a830206af4a67fc75636cf4ac566e3587737a217284173a543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,2731,27933,27934</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22529521$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20033054$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brüggemann, M</creatorcontrib><creatorcontrib>Schrauder, A</creatorcontrib><creatorcontrib>Raff, T</creatorcontrib><creatorcontrib>Pfeifer, H</creatorcontrib><creatorcontrib>Dworzak, M</creatorcontrib><creatorcontrib>Ottmann, O G</creatorcontrib><creatorcontrib>Asnafi, V</creatorcontrib><creatorcontrib>Baruchel, A</creatorcontrib><creatorcontrib>Bassan, R</creatorcontrib><creatorcontrib>Benoit, Y</creatorcontrib><creatorcontrib>Biondi, A</creatorcontrib><creatorcontrib>Cavé, H</creatorcontrib><creatorcontrib>Dombret, H</creatorcontrib><creatorcontrib>Fielding, A K</creatorcontrib><creatorcontrib>Foà, R</creatorcontrib><creatorcontrib>Gökbuget, N</creatorcontrib><creatorcontrib>Goldstone, A H</creatorcontrib><creatorcontrib>Goulden, N</creatorcontrib><creatorcontrib>Henze, G</creatorcontrib><creatorcontrib>Hoelzer, D</creatorcontrib><creatorcontrib>Janka-Schaub, G E</creatorcontrib><creatorcontrib>Macintyre, E A</creatorcontrib><creatorcontrib>Pieters, R</creatorcontrib><creatorcontrib>Rambaldi, A</creatorcontrib><creatorcontrib>Ribera, J-M</creatorcontrib><creatorcontrib>Schmiegelow, K</creatorcontrib><creatorcontrib>Spinelli, O</creatorcontrib><creatorcontrib>Stary, J</creatorcontrib><creatorcontrib>von Stackelberg, A</creatorcontrib><creatorcontrib>Kneba, M</creatorcontrib><creatorcontrib>Schrappe, M</creatorcontrib><creatorcontrib>van Dongen, J J M</creatorcontrib><creatorcontrib>European Working Group for Adult Acute Lymphoblastic Leukemia (EWALL)</creatorcontrib><creatorcontrib>International Berlin-Frankfurt-Münster Study Group (I-BFM-SG)</creatorcontrib><creatorcontrib>also on behalf of the European Working Group for Adult Acute Lymphoblastic Leukemia (EWALL) and the International Berlin–Frankfurt–Münster Study Group (I-BFM-SG)</creatorcontrib><title>Standardized MRD quantification in European ALL trials: Proceedings of the Second International Symposium on MRD assessment in Kiel, Germany, 18-20 September 2008</title><title>Leukemia</title><addtitle>Leukemia</addtitle><addtitle>Leukemia</addtitle><description>Assessment of minimal residual disease (MRD) has acquired a prominent position in European treatment protocols for patients with acute lymphoblastic leukemia (ALL), on the basis of its high prognostic value for predicting outcome and the possibilities for implementation of MRD diagnostics in treatment stratification. Therefore, there is an increasing need for standardization of methodologies and harmonization of terminology. For this purpose, a panel of representatives of all major European study groups on childhood and adult ALL and of international experts on PCR- and flow cytometry-based MRD assessment was built in the context of the Second International Symposium on MRD assessment in Kiel, Germany, 18–20 September 2008. The panel summarized the current state of MRD diagnostics in ALL and developed recommendations on the minimal technical requirements that should be fulfilled before implementation of MRD diagnostics into clinical trials. Finally, a common terminology for a standard description of MRD response and monitoring was established defining the terms ‘complete MRD response’, ‘MRD persistence’ and ‘MRD reappearance’. The proposed MRD terminology may allow a refined and standardized assessment of response to treatment in adult and childhood ALL, and provides a sound basis for the comparison of MRD results between different treatment protocols.</description><subject>Acute lymphoblastic leukemia</subject><subject>Acute lymphocytic leukemia</subject><subject>Biological and medical sciences</subject><subject>Cancer</subject><subject>Cancer Research</subject><subject>Care and treatment</subject><subject>Children</subject><subject>Clinical trials</subject><subject>College campuses</subject><subject>Critical Care Medicine</subject><subject>Flow Cytometry</subject><subject>Fusion Proteins, bcr-abl - genetics</subject><subject>Gene Rearrangement</subject><subject>Genes, Immunoglobulin</subject><subject>Genetic aspects</subject><subject>Health services</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Hematology</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Intensive</subject><subject>Internal Medicine</subject><subject>Jargon</subject><subject>Leukemia</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Lymphatic leukemia</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Minimal residual disease</subject><subject>Neoplasm, Residual - diagnosis</subject><subject>Oncology</subject><subject>Patient outcomes</subject><subject>Pediatrics</subject><subject>Polymerase Chain Reaction</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis</subject><subject>Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy</subject><subject>Relapse</subject><subject>review</subject><subject>Standardization</subject><subject>Terminology</subject><issn>0887-6924</issn><issn>1476-5551</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqN0k1v0zAYB_AIgdgo3Dgjiwm4NMUvsZ1wq8YYE0UgCufIc560nhK7s51D-Th8UhxaVoaYhHKIEv_8f_zyZNlTgmcEs_J1B8OMYlzNqCjvZcekkCLnnJP72TEuS5mLihZH2aMQrjAeB8XD7Ch5xjAvjrMfy6hso3xjvkODPn55i64HZaNpjVbROIuMRWeDdxtQFs0XCxS9UV14gz57pwEaY1cBuRbFNaAlaGcbdGEjePtrturQcttvXDBDj1LYmK9CgBB6sHHM_mCgm6Jz8L2y2ykiZU5xCtpE6C_Bo7TQ8nH2oE0l4cn-Pcm-vTv7evo-X3w6vzidL3ItJI25LKlgLRaCtI0ErEqGKRaqLZSQrZZcMKHTh-ZCAOOllEwqSiQtCyKZ4gWbZK92uRvvrgcIse5N0NB1yoIbQi0LgRPG_yEZExWpeJXkyV_yyg3pcLpQU1FwyUSRFjLJnt-pKOaMMC4PUSvVQW1s66JXeixczyklIm1Q0qRm_1DpaaA36XqgNen_rQkv_5iwBtXFdXDdMF5fuA2nO6i9C8FDW2-86ZXf1gTXYyfWqRPrsRPT1srEn-33NFz20Nzg362XwIs9UEGrrvXKahMOjnJacUqSy3cupCG7An84nDsKo51PLTh4uAlMaDQj-QmBQvoR</recordid><startdate>20100301</startdate><enddate>20100301</enddate><creator>Brüggemann, M</creator><creator>Schrauder, A</creator><creator>Raff, T</creator><creator>Pfeifer, H</creator><creator>Dworzak, M</creator><creator>Ottmann, O G</creator><creator>Asnafi, V</creator><creator>Baruchel, A</creator><creator>Bassan, R</creator><creator>Benoit, Y</creator><creator>Biondi, A</creator><creator>Cavé, H</creator><creator>Dombret, H</creator><creator>Fielding, A K</creator><creator>Foà, R</creator><creator>Gökbuget, N</creator><creator>Goldstone, A H</creator><creator>Goulden, N</creator><creator>Henze, G</creator><creator>Hoelzer, D</creator><creator>Janka-Schaub, G E</creator><creator>Macintyre, E A</creator><creator>Pieters, R</creator><creator>Rambaldi, A</creator><creator>Ribera, J-M</creator><creator>Schmiegelow, K</creator><creator>Spinelli, O</creator><creator>Stary, J</creator><creator>von Stackelberg, A</creator><creator>Kneba, M</creator><creator>Schrappe, M</creator><creator>van Dongen, J J M</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>IQODW</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>7QL</scope><scope>7RV</scope><scope>7T5</scope><scope>7T7</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20100301</creationdate><title>Standardized MRD quantification in European ALL trials: Proceedings of the Second International Symposium on MRD assessment in Kiel, Germany, 18-20 September 2008</title><author>Brüggemann, M ; 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UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</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><jtitle>Leukemia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brüggemann, M</au><au>Schrauder, A</au><au>Raff, T</au><au>Pfeifer, H</au><au>Dworzak, M</au><au>Ottmann, O G</au><au>Asnafi, V</au><au>Baruchel, A</au><au>Bassan, R</au><au>Benoit, Y</au><au>Biondi, A</au><au>Cavé, H</au><au>Dombret, H</au><au>Fielding, A K</au><au>Foà, R</au><au>Gökbuget, N</au><au>Goldstone, A H</au><au>Goulden, N</au><au>Henze, G</au><au>Hoelzer, D</au><au>Janka-Schaub, G E</au><au>Macintyre, E A</au><au>Pieters, R</au><au>Rambaldi, A</au><au>Ribera, J-M</au><au>Schmiegelow, K</au><au>Spinelli, O</au><au>Stary, J</au><au>von Stackelberg, A</au><au>Kneba, M</au><au>Schrappe, M</au><au>van Dongen, J J M</au><aucorp>European Working Group for Adult Acute Lymphoblastic Leukemia (EWALL)</aucorp><aucorp>International Berlin-Frankfurt-Münster Study Group (I-BFM-SG)</aucorp><aucorp>also on behalf of the European Working Group for Adult Acute Lymphoblastic Leukemia (EWALL) and the International Berlin–Frankfurt–Münster Study Group (I-BFM-SG)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Standardized MRD quantification in European ALL trials: Proceedings of the Second International Symposium on MRD assessment in Kiel, Germany, 18-20 September 2008</atitle><jtitle>Leukemia</jtitle><stitle>Leukemia</stitle><addtitle>Leukemia</addtitle><date>2010-03-01</date><risdate>2010</risdate><volume>24</volume><issue>3</issue><spage>521</spage><epage>535</epage><pages>521-535</pages><issn>0887-6924</issn><eissn>1476-5551</eissn><coden>LEUKED</coden><abstract>Assessment of minimal residual disease (MRD) has acquired a prominent position in European treatment protocols for patients with acute lymphoblastic leukemia (ALL), on the basis of its high prognostic value for predicting outcome and the possibilities for implementation of MRD diagnostics in treatment stratification. Therefore, there is an increasing need for standardization of methodologies and harmonization of terminology. For this purpose, a panel of representatives of all major European study groups on childhood and adult ALL and of international experts on PCR- and flow cytometry-based MRD assessment was built in the context of the Second International Symposium on MRD assessment in Kiel, Germany, 18–20 September 2008. The panel summarized the current state of MRD diagnostics in ALL and developed recommendations on the minimal technical requirements that should be fulfilled before implementation of MRD diagnostics into clinical trials. Finally, a common terminology for a standard description of MRD response and monitoring was established defining the terms ‘complete MRD response’, ‘MRD persistence’ and ‘MRD reappearance’. The proposed MRD terminology may allow a refined and standardized assessment of response to treatment in adult and childhood ALL, and provides a sound basis for the comparison of MRD results between different treatment protocols.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>20033054</pmid><doi>10.1038/leu.2009.268</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acute lymphoblastic leukemia Acute lymphocytic leukemia Biological and medical sciences Cancer Cancer Research Care and treatment Children Clinical trials College campuses Critical Care Medicine Flow Cytometry Fusion Proteins, bcr-abl - genetics Gene Rearrangement Genes, Immunoglobulin Genetic aspects Health services Hematologic and hematopoietic diseases Hematology Hospitals Humans Intensive Internal Medicine Jargon Leukemia Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Lymphatic leukemia Medical sciences Medicine Medicine & Public Health Minimal residual disease Neoplasm, Residual - diagnosis Oncology Patient outcomes Pediatrics Polymerase Chain Reaction Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy Relapse review Standardization Terminology |
title | Standardized MRD quantification in European ALL trials: Proceedings of the Second International Symposium on MRD assessment in Kiel, Germany, 18-20 September 2008 |
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