To Örebro University

oru.seÖrebro University Publications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Quality control of flow cytometry data analysis for evaluation of minimal residual disease in bone marrow from acute leukemia patients during treatment
Department of Pathology and Cytology, Karolinska University Hospital, Solna, Sweden.
Department of Clinical Chemistry and Hematology, Kuopio University Hospital, Kuopio, Finland.
Department of Pathology, Rikshospitalet-Radiumhospitalet-HF, Oslo, Norway.
Department of Pathology, Örebro University Hospital (USÖ), Örebro, Sweden.
Show others and affiliations
2009 (English)In: Journal of Pediatric Hematology/Oncology, ISSN 1077-4114, E-ISSN 1536-3678, Vol. 31, no 6, p. 406-15Article in journal (Refereed) Published
Abstract [en]

Low levels of leukemia cells in the bone marrow, minimal residual disease (MRD), are considered to be a powerful indicator of treatment response in acute lymphatic leukemia (ALL). A Nordic quality assurance program, aimed on standardization of the flow cytometry MRD analysis, has been established before implementation of MRD at cutoff level 10 as one of stratifying parameters in next Nordic Society of Pediatric Hematology and Oncology (NOPHO) treatment program for ALL. In 4 quality control (QC) rounds 15 laboratories determined the MRD levels in 48 follow-up samples from 12 ALL patients treated according to NOPHO 2000. Analysis procedures were standardized. For each QC round a compact disc containing data in list-mode files was sent out and results were submitted to a central laboratory. At cutoff level 10, which will be applied for clinical decisions, laboratories obtained a high concordance (91.6%). If cutoff level 10 was applied, the concordance would be lower (85.3%). The continuing standardization resulted in better concordance in QC3 and QC4 compared with QC1 and QC2. The concordance was higher in precursor B as compared with T-cell ALL. We conclude that after standardization, flow cytometry MRD detection can be reliably applied in international, multicenter treatment protocols.

Place, publisher, year, edition, pages
Lippincott Williams & Wilkins, 2009. Vol. 31, no 6, p. 406-15
National Category
Hematology
Identifiers
URN: urn:nbn:se:oru:diva-110578DOI: 10.1097/MPH.0b013e3181a1c0e8PubMedID: 19648789Scopus ID: 2-s2.0-67651205898OAI: oai:DiVA.org:oru-110578DiVA, id: diva2:1823756
Available from: 2024-01-03 Created: 2024-01-03 Last updated: 2024-01-08Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textPubMedScopus

Authority records

Axelsson, Susanne

Search in DiVA

By author/editor
Axelsson, Susanne
In the same journal
Journal of Pediatric Hematology/Oncology
Hematology

Search outside of DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 27 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf