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Standardization of molecular monitoring of CML: results and recommendations from the European treatment and outcome study

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023736%3A_____%2F22%3A00013409" target="_blank" >RIV/00023736:_____/22:00013409 - isvavai.cz</a>

  • Alternative codes found

    RIV/65269705:_____/22:00076133 RIV/00216224:14110/22:00128094

  • Result on the web

    <a href="https://doi.org/10.1038/s41375-022-01607-z" target="_blank" >https://doi.org/10.1038/s41375-022-01607-z</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1038/s41375-022-01607-z" target="_blank" >10.1038/s41375-022-01607-z</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Standardization of molecular monitoring of CML: results and recommendations from the European treatment and outcome study

  • Original language description

    Standardized monitoring of BCR::ABL1 mRNA levels is essential for the management of chronic myeloid leukemia (CML) patients. From 2016 to 2021 the European Treatment and Outcome Study for CML (EUTOS) explored the use of secondary, lyophilized cell-based BCR::ABL1 reference panels traceable to the World Health Organization primary reference material to standardize and validate local laboratory tests. Panels were used to assign and validate conversion factors (CFs) to the International Scale and assess the ability of laboratories to assess deep molecular response (DMR). The study also explored aspects of internal quality control. The percentage of EUTOS reference laboratories (n = 50) with CFs validated as optimal or satisfactory increased from 67.5% to 97.6% and 36.4% to 91.7% for ABL1 and GUSB, respectively, during the study period and 98% of laboratories were able to detect MR4.5 in most samples. Laboratories with unvalidated CFs had a higher coefficient of variation for BCR::ABL1(IS) and some laboratories had a limit of blank greater than zero which could affect the accurate reporting of DMR. Our study indicates that secondary reference panels can be used effectively to obtain and validate CFs in a manner equivalent to sample exchange and can also be used to monitor additional aspects of quality assurance.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30205 - Hematology

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2022

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Leukemia

  • ISSN

    0887-6924

  • e-ISSN

  • Volume of the periodical

    36

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    9

  • Pages from-to

    1834-1842

  • UT code for WoS article

    000802314200002

  • EID of the result in the Scopus database

    2-s2.0-85130820056