One-point flow cytometric MRD measurement to identify children with excellent outcome after intermediate-risk BCP-ALL: results of the ALL-MB 2008 study
Background Measurement of minimal residual disease (MRD) with multicolor flow cytometry (MFC) has become an important tool in childhood acute lymphoblastic leukemia (ALL), mainly to identify rapid responders and reduce their therapy intensity. Protocols of the Moscow–Berlin (MB) group use a compara...
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creator | Popov, Alexander Henze, Guenter Roumiantseva, Julia Budanov, Oleg Belevtsev, Mikhail Verzhbitskaya, Tatiana Boyakova, Elena Movchan, Liudmila Tsaur, Grigory Fadeeva, Maria Lagoyko, Svetlana Zharikova, Liudmila Miakova, Natalia Litvinov, Dmitry Khlebnikova, Olga Streneva, Olga Stolyarova, Elena Ponomareva, Natalia Novichkova, Galina Fechina, Larisa Aleinikova, Olga Karachunskiy, Alexander |
description | Background
Measurement of minimal residual disease (MRD) with multicolor flow cytometry (MFC) has become an important tool in childhood acute lymphoblastic leukemia (ALL), mainly to identify rapid responders and reduce their therapy intensity. Protocols of the Moscow–Berlin (MB) group use a comparatively low (for standard risk; SR) or moderate (for intermediate risk; ImR) treatment intensity from the onset, based on initial patient characteristics. Recently, we reported that 90% of SR patients—50% B cell precursor (BCP-ALL)—MFC-MRD negative at end of induction (EOI)—had 95% event-free survival (EFS).
Methods
In the present study, we applied this method to children with initial ImR features.
Results
In study MB 2008, 1105 children—32% of BCP-ALL patients—were assigned to the ImR group. Of these, 227 were treated in clinics affiliated with MFC laboratories of the MB group network, and included in this MFC-MRD pilot study. A single-point MFC-MRD measurement at the EOI with the threshold of 0.01% identified 65% of patients—20% of all BCP-ALL patients—with EFS of 93.5%.
Conclusion
Taking both studies together, the combination of clinical parameters and a one-point MRD measurement identifies 70% of BCP-ALL patients with an excellent outcome after low- or moderate-intensity therapy and avoids overtreatment of a significant proportion of patients. |
doi_str_mv | 10.1007/s00432-022-04378-3 |
format | Article |
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Measurement of minimal residual disease (MRD) with multicolor flow cytometry (MFC) has become an important tool in childhood acute lymphoblastic leukemia (ALL), mainly to identify rapid responders and reduce their therapy intensity. Protocols of the Moscow–Berlin (MB) group use a comparatively low (for standard risk; SR) or moderate (for intermediate risk; ImR) treatment intensity from the onset, based on initial patient characteristics. Recently, we reported that 90% of SR patients—50% B cell precursor (BCP-ALL)—MFC-MRD negative at end of induction (EOI)—had 95% event-free survival (EFS).
Methods
In the present study, we applied this method to children with initial ImR features.
Results
In study MB 2008, 1105 children—32% of BCP-ALL patients—were assigned to the ImR group. Of these, 227 were treated in clinics affiliated with MFC laboratories of the MB group network, and included in this MFC-MRD pilot study. A single-point MFC-MRD measurement at the EOI with the threshold of 0.01% identified 65% of patients—20% of all BCP-ALL patients—with EFS of 93.5%.
Conclusion
Taking both studies together, the combination of clinical parameters and a one-point MRD measurement identifies 70% of BCP-ALL patients with an excellent outcome after low- or moderate-intensity therapy and avoids overtreatment of a significant proportion of patients.</description><identifier>ISSN: 0171-5216</identifier><identifier>EISSN: 1432-1335</identifier><identifier>DOI: 10.1007/s00432-022-04378-3</identifier><identifier>PMID: 36169717</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Acute lymphoblastic leukemia ; Bone marrow ; Cancer Research ; Cancer therapies ; Children ; Drug dosages ; Flow cytometry ; Hematology ; Immunology ; Induction therapy ; Internal Medicine ; Laboratories ; Leukemia ; Lymphatic leukemia ; Medical research ; Medicine ; Medicine & Public Health ; Minimal residual disease ; Oncology ; Patients ; Pediatrics ; Pilot projects</subject><ispartof>Journal of cancer research and clinical oncology, 2023-07, Vol.149 (8), p.4629-4637</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022. Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-64e6185d6e05656e4cc5f2b36eac13f1219732dbeef8784ebb2d7905f27118e3</citedby><cites>FETCH-LOGICAL-c375t-64e6185d6e05656e4cc5f2b36eac13f1219732dbeef8784ebb2d7905f27118e3</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/s00432-022-04378-3$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00432-022-04378-3$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36169717$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Popov, Alexander</creatorcontrib><creatorcontrib>Henze, Guenter</creatorcontrib><creatorcontrib>Roumiantseva, Julia</creatorcontrib><creatorcontrib>Budanov, Oleg</creatorcontrib><creatorcontrib>Belevtsev, Mikhail</creatorcontrib><creatorcontrib>Verzhbitskaya, Tatiana</creatorcontrib><creatorcontrib>Boyakova, Elena</creatorcontrib><creatorcontrib>Movchan, Liudmila</creatorcontrib><creatorcontrib>Tsaur, Grigory</creatorcontrib><creatorcontrib>Fadeeva, Maria</creatorcontrib><creatorcontrib>Lagoyko, Svetlana</creatorcontrib><creatorcontrib>Zharikova, Liudmila</creatorcontrib><creatorcontrib>Miakova, Natalia</creatorcontrib><creatorcontrib>Litvinov, Dmitry</creatorcontrib><creatorcontrib>Khlebnikova, Olga</creatorcontrib><creatorcontrib>Streneva, Olga</creatorcontrib><creatorcontrib>Stolyarova, Elena</creatorcontrib><creatorcontrib>Ponomareva, Natalia</creatorcontrib><creatorcontrib>Novichkova, Galina</creatorcontrib><creatorcontrib>Fechina, Larisa</creatorcontrib><creatorcontrib>Aleinikova, Olga</creatorcontrib><creatorcontrib>Karachunskiy, Alexander</creatorcontrib><title>One-point flow cytometric MRD measurement to identify children with excellent outcome after intermediate-risk BCP-ALL: results of the ALL-MB 2008 study</title><title>Journal of cancer research and clinical oncology</title><addtitle>J Cancer Res Clin Oncol</addtitle><addtitle>J Cancer Res Clin Oncol</addtitle><description>Background
Measurement of minimal residual disease (MRD) with multicolor flow cytometry (MFC) has become an important tool in childhood acute lymphoblastic leukemia (ALL), mainly to identify rapid responders and reduce their therapy intensity. Protocols of the Moscow–Berlin (MB) group use a comparatively low (for standard risk; SR) or moderate (for intermediate risk; ImR) treatment intensity from the onset, based on initial patient characteristics. Recently, we reported that 90% of SR patients—50% B cell precursor (BCP-ALL)—MFC-MRD negative at end of induction (EOI)—had 95% event-free survival (EFS).
Methods
In the present study, we applied this method to children with initial ImR features.
Results
In study MB 2008, 1105 children—32% of BCP-ALL patients—were assigned to the ImR group. Of these, 227 were treated in clinics affiliated with MFC laboratories of the MB group network, and included in this MFC-MRD pilot study. A single-point MFC-MRD measurement at the EOI with the threshold of 0.01% identified 65% of patients—20% of all BCP-ALL patients—with EFS of 93.5%.
Conclusion
Taking both studies together, the combination of clinical parameters and a one-point MRD measurement identifies 70% of BCP-ALL patients with an excellent outcome after low- or moderate-intensity therapy and avoids overtreatment of a significant proportion of patients.</description><subject>Acute lymphoblastic leukemia</subject><subject>Bone marrow</subject><subject>Cancer Research</subject><subject>Cancer therapies</subject><subject>Children</subject><subject>Drug dosages</subject><subject>Flow cytometry</subject><subject>Hematology</subject><subject>Immunology</subject><subject>Induction therapy</subject><subject>Internal Medicine</subject><subject>Laboratories</subject><subject>Leukemia</subject><subject>Lymphatic leukemia</subject><subject>Medical research</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Minimal residual disease</subject><subject>Oncology</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Pilot projects</subject><issn>0171-5216</issn><issn>1432-1335</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kctu1DAUhi0EotPCC7BAltiwMfgSX8KuHSggTVWEurcS55hxSeLBdlTmSXhdPEwBiQULy_Y53__78iP0jNFXjFL9OlPaCE4or6MR2hDxAK3YocSEkA_RijLNiORMnaDTnG9p3UvNH6MToZhqNdMr9ON6BrKLYS7Yj_EOu32JE5QUHL76_BZP0OUlwQS1XyIOQ10Ev8duG8YhwYzvQtli-O5gHA9MXIqretz5AglXV0gTDKErQFLIX_HF-hM532ze4AR5GUvG0eOyBVxr5OoCc0oNzmUZ9k_QI9-NGZ7ez2fo5vLdzfoD2Vy__7g-3xAntCxENaCYkYMCKpVU0DgnPe-Fgs4x4RlnrRZ86AG80aaBvueDbmllNGMGxBl6ebTdpfhtgVzsFPLhMd0Mccm2YqZVTBpa0Rf_oLdxSXO9nOVGaNVwrdtK8SPlUsw5gbe7FKYu7S2j9pCaPaZma2r2V2pWVNHze-ulr9_1R_I7pgqII5Bra_4C6e_Z_7H9CTnWokQ</recordid><startdate>20230701</startdate><enddate>20230701</enddate><creator>Popov, Alexander</creator><creator>Henze, Guenter</creator><creator>Roumiantseva, Julia</creator><creator>Budanov, Oleg</creator><creator>Belevtsev, Mikhail</creator><creator>Verzhbitskaya, Tatiana</creator><creator>Boyakova, Elena</creator><creator>Movchan, Liudmila</creator><creator>Tsaur, Grigory</creator><creator>Fadeeva, Maria</creator><creator>Lagoyko, Svetlana</creator><creator>Zharikova, Liudmila</creator><creator>Miakova, Natalia</creator><creator>Litvinov, Dmitry</creator><creator>Khlebnikova, Olga</creator><creator>Streneva, Olga</creator><creator>Stolyarova, Elena</creator><creator>Ponomareva, Natalia</creator><creator>Novichkova, Galina</creator><creator>Fechina, Larisa</creator><creator>Aleinikova, Olga</creator><creator>Karachunskiy, Alexander</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20230701</creationdate><title>One-point flow cytometric MRD measurement to identify children with excellent outcome after intermediate-risk BCP-ALL: results of the ALL-MB 2008 study</title><author>Popov, Alexander ; Henze, Guenter ; Roumiantseva, Julia ; Budanov, Oleg ; Belevtsev, Mikhail ; Verzhbitskaya, Tatiana ; Boyakova, Elena ; Movchan, Liudmila ; Tsaur, Grigory ; Fadeeva, Maria ; Lagoyko, Svetlana ; Zharikova, Liudmila ; Miakova, Natalia ; Litvinov, Dmitry ; Khlebnikova, Olga ; Streneva, Olga ; Stolyarova, Elena ; Ponomareva, Natalia ; Novichkova, Galina ; Fechina, Larisa ; Aleinikova, Olga ; Karachunskiy, Alexander</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-64e6185d6e05656e4cc5f2b36eac13f1219732dbeef8784ebb2d7905f27118e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Acute lymphoblastic leukemia</topic><topic>Bone marrow</topic><topic>Cancer Research</topic><topic>Cancer therapies</topic><topic>Children</topic><topic>Drug dosages</topic><topic>Flow cytometry</topic><topic>Hematology</topic><topic>Immunology</topic><topic>Induction therapy</topic><topic>Internal Medicine</topic><topic>Laboratories</topic><topic>Leukemia</topic><topic>Lymphatic leukemia</topic><topic>Medical research</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Minimal residual disease</topic><topic>Oncology</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Pilot projects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Popov, Alexander</creatorcontrib><creatorcontrib>Henze, Guenter</creatorcontrib><creatorcontrib>Roumiantseva, Julia</creatorcontrib><creatorcontrib>Budanov, Oleg</creatorcontrib><creatorcontrib>Belevtsev, Mikhail</creatorcontrib><creatorcontrib>Verzhbitskaya, Tatiana</creatorcontrib><creatorcontrib>Boyakova, Elena</creatorcontrib><creatorcontrib>Movchan, Liudmila</creatorcontrib><creatorcontrib>Tsaur, Grigory</creatorcontrib><creatorcontrib>Fadeeva, Maria</creatorcontrib><creatorcontrib>Lagoyko, Svetlana</creatorcontrib><creatorcontrib>Zharikova, 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Olga</au><au>Streneva, Olga</au><au>Stolyarova, Elena</au><au>Ponomareva, Natalia</au><au>Novichkova, Galina</au><au>Fechina, Larisa</au><au>Aleinikova, Olga</au><au>Karachunskiy, Alexander</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>One-point flow cytometric MRD measurement to identify children with excellent outcome after intermediate-risk BCP-ALL: results of the ALL-MB 2008 study</atitle><jtitle>Journal of cancer research and clinical oncology</jtitle><stitle>J Cancer Res Clin Oncol</stitle><addtitle>J Cancer Res Clin Oncol</addtitle><date>2023-07-01</date><risdate>2023</risdate><volume>149</volume><issue>8</issue><spage>4629</spage><epage>4637</epage><pages>4629-4637</pages><issn>0171-5216</issn><eissn>1432-1335</eissn><abstract>Background
Measurement of minimal residual disease (MRD) with multicolor flow cytometry (MFC) has become an important tool in childhood acute lymphoblastic leukemia (ALL), mainly to identify rapid responders and reduce their therapy intensity. Protocols of the Moscow–Berlin (MB) group use a comparatively low (for standard risk; SR) or moderate (for intermediate risk; ImR) treatment intensity from the onset, based on initial patient characteristics. Recently, we reported that 90% of SR patients—50% B cell precursor (BCP-ALL)—MFC-MRD negative at end of induction (EOI)—had 95% event-free survival (EFS).
Methods
In the present study, we applied this method to children with initial ImR features.
Results
In study MB 2008, 1105 children—32% of BCP-ALL patients—were assigned to the ImR group. Of these, 227 were treated in clinics affiliated with MFC laboratories of the MB group network, and included in this MFC-MRD pilot study. A single-point MFC-MRD measurement at the EOI with the threshold of 0.01% identified 65% of patients—20% of all BCP-ALL patients—with EFS of 93.5%.
Conclusion
Taking both studies together, the combination of clinical parameters and a one-point MRD measurement identifies 70% of BCP-ALL patients with an excellent outcome after low- or moderate-intensity therapy and avoids overtreatment of a significant proportion of patients.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>36169717</pmid><doi>10.1007/s00432-022-04378-3</doi><tpages>9</tpages></addata></record> |
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subjects | Acute lymphoblastic leukemia Bone marrow Cancer Research Cancer therapies Children Drug dosages Flow cytometry Hematology Immunology Induction therapy Internal Medicine Laboratories Leukemia Lymphatic leukemia Medical research Medicine Medicine & Public Health Minimal residual disease Oncology Patients Pediatrics Pilot projects |
title | One-point flow cytometric MRD measurement to identify children with excellent outcome after intermediate-risk BCP-ALL: results of the ALL-MB 2008 study |
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