PFEIFER, H., G. CAZZANIGA, V. H. J VAN DER VELDEN, J. M. CAYUELE, B. SCHAFER, O. SPINELLI, S. AKIKI, S. AVIGAD, I. BENDIT, K. BORG, H. CAVE, L. ELIA, S. C. RESHMI, G. GERRARD, S. HAYETTE, M. HERMANSON, A. JUH, Tomáš JURČEK, M. C. CHILLON, C. HOMBURG, G. MARTINELLI, V. KAIRISTO, T. LANGEN, T. LION, M. C. MUELLER, F. PANE, L. RAI, C. DAMM-WELK, T. SACHA, S. SCHNITTGER, T. TOULOUMENIDOU, H. VALERHAUGEN, P. VANDENBERGHE, J. ZUNA, H. SERVER, E. HERRMANN, S. MARKOVIC, J. J. M VAN DONGEN and O. G. OTTMANN. Standardisation and consensus guidelines for minimal residual disease assessment in Philadelphia-positive acute lymphoblastic leukemia (Ph plus ALL) by real-time quantitative reverse transcriptase PCR of e1a2 BCR-ABL1. Leukemia. London: Nature Publishing Group, 2019, vol. 33, No 8, p. 1910-1922. ISSN 0887-6924. Available from: https://dx.doi.org/10.1038/s41375-019-0413-0.
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Original name Standardisation and consensus guidelines for minimal residual disease assessment in Philadelphia-positive acute lymphoblastic leukemia (Ph plus ALL) by real-time quantitative reverse transcriptase PCR of e1a2 BCR-ABL1
Authors PFEIFER, H. (276 Germany, guarantor), G. CAZZANIGA (380 Italy), V. H. J VAN DER VELDEN (528 Netherlands), J. M. CAYUELE (250 France), B. SCHAFER (756 Switzerland), O. SPINELLI (380 Italy), S. AKIKI (826 United Kingdom of Great Britain and Northern Ireland), S. AVIGAD (376 Israel), I. BENDIT (76 Brazil), K. BORG (616 Poland), H. CAVE (250 France), L. ELIA (380 Italy), S. C. RESHMI (840 United States of America), G. GERRARD (826 United Kingdom of Great Britain and Northern Ireland), S. HAYETTE (250 France), M. HERMANSON (752 Sweden), A. JUH (702 Singapore), Tomáš JURČEK (203 Czech Republic, belonging to the institution), M. C. CHILLON (724 Spain), C. HOMBURG (528 Netherlands), G. MARTINELLI (380 Italy), V. KAIRISTO (246 Finland), T. LANGEN (276 Germany), T. LION (40 Austria), M. C. MUELLER (528 Netherlands), F. PANE (380 Italy), L. RAI (826 United Kingdom of Great Britain and Northern Ireland), C. DAMM-WELK (276 Germany), T. SACHA (616 Poland), S. SCHNITTGER (276 Germany), T. TOULOUMENIDOU (300 Greece), H. VALERHAUGEN (56 Belgium), P. VANDENBERGHE (56 Belgium), J. ZUNA (203 Czech Republic), H. SERVER (276 Germany), E. HERRMANN (276 Germany), S. MARKOVIC (276 Germany), J. J. M VAN DONGEN (528 Netherlands) and O. G. OTTMANN (826 United Kingdom of Great Britain and Northern Ireland).
Edition Leukemia, London, Nature Publishing Group, 2019, 0887-6924.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30204 Oncology
Country of publisher Slovenia
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 8.665
RIV identification code RIV/00216224:14110/19:00111758
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1038/s41375-019-0413-0
UT WoS 000479118400006
Keywords in English STEM-CELL TRANSPLANTATION; POLYMERASE-CHAIN-REACTION; FUSION GENE TRANSCRIPTS; BCR-ABL TRANSCRIPTS; HARMONIZING CURRENT METHODOLOGY; TYROSINE KINASE INHIBITORS; ADULT PATIENTS; T-CELL; PERIPHERAL-BLOOD; INTENSITY CHEMOTHERAPY
Tags 14110212, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 17/12/2019 12:23.
Abstract
Minimal residual disease (MRD) is a powerful prognostic factor in acute lymphoblastic leukemia (ALL) and is used for patient stratification and treatment decisions, but its precise role in Philadelphia chromosome positive ALL is less clear. This uncertainty results largely from methodological differences relating to the use of real-time quantitative PCR (qRT-PCR) to measure BCR-ABL1 transcript levels for MRD analysis. We here describe the first results by the EURO-MRD consortium on standardization of qRT-PCR for the e1a2 BCR-ABL1 transcript in Ph + ALL, designed to overcome the lack of standardisation of laboratory procedures and data interpretation. Standardised use of EAC primer/probe sets and of centrally prepared plasmid standards had the greatest impact on reducing interlaboratory variability. In QC1 the proportion of analyses with BCR-ABL1/ABL1 ratios within half a log difference were 40/67 (60%) and 52/67 (78%) at 10(-3) and 36/67 (53%) and 53/67 (79%) at 10(-4)BCR-ABL1/ABL1. Standardized RNA extraction, cDNA synthesis and cycler platforms did not improve results further, whereas stringent application of technical criteria for assay quality and uniform criteria for data interpretation and reporting were essential. We provide detailed laboratory recommendations for the standardized MRD analysis in routine diagnostic settings and in multicenter clinical trials for Ph + ALL.
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