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FältnamnIndikatorerMetadata
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001oai:gup.ub.gu.se/299424
003SwePub
008240528s2021 | |||||||||||000 ||eng|
009oai:DiVA.org:umu-178333
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024a https://gup.ub.gu.se/publication/2994242 URI
024a https://doi.org/10.1038/s41375-020-01100-52 DOI
024a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-1783332 URI
024a https://lup.lub.lu.se/record/7bab7e42-4df7-4f74-8d4f-140962a259212 URI
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4545172 URI
040 a (SwePub)gud (SwePub)umud (SwePub)lud (SwePub)uu
041 a eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Modvig, Su Copenhagen University Hospital,Vilnius University,Copenhagen Univ Hosp, Rigshosp, Dept Clin Immunol, Copenhagen, Denmark.,Vilnius Univ Hosp, Santaros Klin, Hematol Oncol & Transfus Med Ctr, Vilnius, Lithuania.4 aut
2451 0a Value of flow cytometry for MRD-based relapse prediction in B-cell precursor ALL in a multicenter setting.
264 c 2020-12-14
264 1b Springer Science and Business Media LLC,c 2021
520 a PCR of TCR/Ig gene rearrangements is considered the method of choice for minimal residual disease (MRD) quantification in BCP-ALL, but flow cytometry analysis of leukemia-associated immunophenotypes (FCM-MRD) is faster and biologically more informative. FCM-MRD performed in 18 laboratories across seven countries was used for risk stratification of 1487 patients with BCP-ALL enrolled in the NOPHO ALL2008 protocol. When no informative FCM-marker was available, risk stratification was based on real-time quantitative PCR. An informative FCM-marker was found in 96.2% and only two patients (0.14%) had non-informative FCM and non-informative PCR-markers. The overall 5-year event-free survival was 86.1% with a cumulative incidence of relapse (CIR5y) of 9.5%. FCM-MRD levels on days 15 (HzR 4.0, p<0.0001), 29 (HzR 2.7, p<0.0001), and 79 (HzR 3.5, p<0.0001) associated with hazard of relapse adjusted for age, cytogenetics, and WBC. The early (day 15) response associated with CIR5y adjusted for day 29 FCM-MRD, with higher levels in adults (median 2.4×10-2 versus 5.2×10-3, p<0.0001). Undetectable FCM- and/or PCR-MRD on day 29 identified patients with a very good outcome (CIR5y=3.2%). For patients who did not undergo transplantation, day 79 FCM-MRD>10-4 associated with a CIR5y=22.1%. In conclusion, FCM-MRD performed in a multicenter setting is a clinically useful method for MRD-based treatment stratification in BCP-ALL.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Pediatrik0 (SwePub)302212 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Pediatrics0 (SwePub)302212 hsv//eng
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Cancer och onkologi0 (SwePub)302032 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Cancer and Oncology0 (SwePub)302032 hsv//eng
700a Hallböök, Heleneu Uppsala universitet,Uppsala University,Copenhagen University Hospital,Oslo university hospital,Hematologi,Copenhagen Univ Hosp, Rigshosp, Dept Clin Immunol, Copenhagen, Denmark.,Oslo Univ Hosp, Dept Pathol, Lab Mol Pathol, Oslo, Norway.4 aut0 (Swepub:uu)helehall
700a Madsen, H Ou Umeå University,Umeå Univ, Dept Med Biosci, Pathol, Umeå, Sweden.4 aut
700a Siitonen, Su University of Helsinki,University of Copenhagen,Univ Helsinki, Clin Chem, Helsinki, Finland.;Helsinki Univ Hosp, Helsinki, Finland.,Univ Copenhagen, Sect Biostat, Copenhagen, Denmark.4 aut
700a Rosthøj, S4 aut
700a Tierens, Au University of Toronto,Oslo university hospital,Univ Hlth Network, Lab Med Program, Toronto, ON, Canada.;Univ Toronto, Toronto, ON, Canada.;Univ Hosp Oslo, Dept Pathol, Oslo, Norway.4 aut
700a Juvonen, Vu University of Turku,Univ Turku, Dept Clin Chem, Turku, Finland.;Univ Turku, Lab Div, Turku, Finland.;Turku Univ Hosp, Turku, Finland.4 aut
700a Osnes, L T Nu Oslo university hospital,Herlev Hospital,Oslo Univ Hosp, Dept Immunol, Oslo, Norway.,Herlev Univ Hosp, Dept Hematol, Herlev, Denmark.4 aut
700a Vålerhaugen, H4 aut
700a Hultdin, Magnusu Umeå universitet,Patologi4 aut0 (Swepub:umu)magn0001
700a Matuzeviciene, Ru Vilnius University,Vilnius Univ, Inst Biomed Sci, Fac Med, Dept Physiol Biochem Microbiol & Lab Med, Vilnius, Lithuania.;Vilnius Univ Hosp, Santaros Klin, Ctr Lab Med, Vilnius, Lithuania.4 aut
700a Stoskus, M4 aut
700a Ehinger, M.u Lund University,Lunds universitet,Uppsala University,Patologi, Lund,Sektion V,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Pathology, Lund,Section V,Department of Clinical Sciences, Lund,Faculty of Medicine,Skåne University Hospital,Skane Univ Hosp, Dept Clin Genet & Pathol, Lund, Sweden.;Lund Univ, Dept Clin Sci Oncol & Pathol, Lund, Sweden.4 aut0 (Swepub:lu)efor-meh
700a Lilleorg, Au North Estonia Medical Centre,North Estonia Med Ctr, Dept Clin Immunol, Tallinn, Estonia.4 aut
700a Ehinger, M4 aut
700a Norén-Nyström, Ulrikau Umeå University,Umeå universitet,Pediatrik,Umeå Univ, Dept Clin Sci, Pediat, Umeå, Sweden.4 aut0 (Swepub:umu)kagr0007
700a Toft, N4 aut
700a Taskinen, Mu Helsinki University Central Hospital,Helsinki Univ Hosp, Div Pediat Hematol Oncol & Stem Cell Transplantat, Helsinki, Finland.4 aut
700a Jónsson, O Gu National University Hospital of Iceland,Landspitali Univ Hosp, Childrens Hosp, Reykjavik, Iceland.4 aut
700a Pruunsild, Ku Tallinn Children's Hospital,Tallinn Childrens Hosp, Tallinn, Estonia.4 aut
700a Vaitkeviciene, Gu Vilnius University,Vilnius Univ Hosp, Santariskiu Klin, Childrens Hosp, Vilnius, Lithuania.4 aut
700a Vettenranta, Ku University of Helsinki,Univ Helsinki, Helsinki, Finland.;Univ Helsinki, Childrens Hosp, Helsinki, Finland.4 aut
700a Lund, Bu St. Olav’s University Hospital,St Olavs Univ Hosp, Dept Pediat, Trondheim, Norway.;NTNU, Dept Clin & Mol Med, Trondheim, Norway.4 aut
700a Abrahamsson, Jonas,d 1954u Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper, Avdelningen för pediatrik,Institute of Clinical Sciences, Department of Pediatrics,Sahlgrenska University Hospital,Sahlgrens Univ Hosp, Inst Clin Sci, Dept Pediat, Gothenburg, Sweden.4 aut0 (Swepub:gu)xabrjo
700a Porwit, A.u Lund University,Lunds universitet,Patologi, Lund,Sektion V,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Pathology, Lund,Section V,Department of Clinical Sciences, Lund,Faculty of Medicine,Lund Univ, Fac Med, Dept Clin Sci, Div Oncol & Pathol, Lund, Sweden.4 aut0 (Swepub:lu)an6742po
700a Schmiegelow, Ku Copenhagen University Hospital,Copenhagen Univ Hosp, Rigshosp, Dept Pediat & Adolescent Med, Copenhagen, Denmark.;Univ Copenhagen, Inst Clin Med, Fac Med, Copenhagen, Denmark.4 aut
700a Marquart, H V4 aut
700a Marincevic, Millaray,d 1983-u Uppsala universitet,Klinisk och experimentell patologi4 aut0 (Swepub:uu)milma629
710a Copenhagen University Hospitalb Vilnius University4 org
773t Leukemiad : Springer Science and Business Media LLCg 35, s. 1894-1906q 35<1894-1906x 1476-5551x 0887-6924
856u https://www.nature.com/articles/s41375-020-01100-5.pdf
856u https://doi.org/10.1038/s41375-020-01100-5y Fulltext
856u https://umu.diva-portal.org/smash/get/diva2:1516830/FULLTEXT02.pdfx primaryx Raw objecty fulltext:print
856u http://dx.doi.org/10.1038/s41375-020-01100-5x freey FULLTEXT
856u https://uu.diva-portal.org/smash/get/diva2:1598564/FULLTEXT01.pdfx primaryx Raw objecty fulltext:print
8564 8u https://gup.ub.gu.se/publication/299424
8564 8u https://doi.org/10.1038/s41375-020-01100-5
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-178333
8564 8u https://lup.lub.lu.se/record/7bab7e42-4df7-4f74-8d4f-140962a25921
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-454517

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