Tytuł pozycji:
Go with the flow - early assessment of measurable residual disease in children with acute lymphoblastic leukemia treated according to ALL IC-BFM2009
- Tytuł:
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Go with the flow - early assessment of measurable residual disease in children with acute lymphoblastic leukemia treated according to ALL IC-BFM2009
- Autorzy:
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Rygielska, Monika
Pawińska-Wąsikowska, Katarzyna
Klekawka, Tomasz
Książek, Teofila
Wieczorek, Aleksandra
Skoczeń, Szymon
Balwierz, Walentyna
Sadowska, Beata
Bukowska-Straková, Karolina
Surman, Marta
- Data publikacji:
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2022
- Słowa kluczowe:
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acute lymphoblastic leukemia
blast cell clearance
children
flow cytometry
minimal or measurable residual disease
- Język:
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angielski
- ISBN, ISSN:
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20726694
- Prawa:
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http://creativecommons.org/licenses/by/4.0/legalcode.pl
Udzielam licencji. Uznanie autorstwa 4.0 Międzynarodowa
- Linki:
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https://www.mdpi.com/2072-6694/14/21/5359  Link otwiera się w nowym oknie
- Dostawca treści:
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Repozytorium Uniwersytetu Jagiellońskiego
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Measurable residual disease (MRD) is a well-known tool for the evaluation of the early response to treatment in patients with acute lymphoblastic leukemia (ALL). In respect to predicting the relapse the most informative cut-off and time point of MRD measurement during therapy were evaluated in our study. Between 1 January 2013 and 31 December 2019, multiparametric flow cytometry (MFC) MRD was measured in the bone marrow of 140 children with ALL treated according to the ALL IC-BFM2009 protocol. The MRD cut-off of 0.1% and day 33, end of induction, were the most discriminatory for all patients. Patients with negative MRD on day 15 and 33 had a higher 5-year overall survival—OS (100%) and a higher relapse-free survival—RFS rate (97.6%) than those with positive levels of MRD (≥0.01%) at both time points (77.8% and 55.6%, p = 0.002 and 0.001, respectively). Most patients with residual disease below 0.1% on day 15 exhibit hyperdiploidy or ETV6-RUNX1 in ALL cells. Measurement of MRD at early time points can be used with simplified genetic analysis to better identify low and high-risk patients, allowing personalized therapies and further improvement in outcomes in pediatric ALL.