Evidence map›Paper›PMID 35600149›Full record

ArticleCentral-European journal of immunology2022

Expression of CD73 on leukemic blasts increases during follow-up - a promising candidate marker for minimal residual disease detection in pediatric B-cell precursor acute lymphoblastic leukemia.

Łukasz Słota, Łukasz Sędek, Jan Kulis, Bartosz Perkowski, Iwona Malinowska, Joanna Zawitkowska, Bernarda Kazanowska, Katarzyna Derwich, Maciej Niedźwiecki, Agnieszka Mizia-Malarz and 10 more

Open access · goldAbstract read
In one paragraph

Article in Central-European journal of immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 5 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 8 institutions in 1 country.

Łukasz SłotaDepartment of Pediatric Hematology and Oncology, Medical University of Silesia, Katowice, Poland.
Łukasz SędekDepartment of Microbiology and Immunology, Medical University of Silesia, Katowice, Poland.
Jan KulisDepartment of Pediatric Hematology and Oncology, Medical University of Silesia, Katowice, Poland.
Bartosz PerkowskiDepartment of Pediatric Hematology and Oncology, Medical University of Silesia, Katowice, Poland.
Iwona MalinowskaDepartment of Pediatrics, Hematology and Oncology, Medical University of Warsaw, Poland.
Joanna ZawitkowskaDepartment of Pediatric, Hematology, Oncology and Transplantology, Medical University of Lublin, Poland.
Bernarda KazanowskaDepartment of Pediatric Transplantology, Oncology, Hematology, Medical University of Wrocław, Poland.
Katarzyna DerwichDepartment of Pediatric Oncology, Hematology and Transplantology, Medical University of Poznań, Poland.
Maciej NiedźwieckiDepartment of Pediatrics, Hematology, Oncology and Endocrinology, Medical University of Gdańsk, Poland.
Agnieszka Mizia-MalarzDepartment of Pediatric Oncology, Hematology and Chemotherapy, Medical University of Silesia, Katowice, Poland.
Katarzyna Muszyńska-RosłanDepartment of Pediatric Oncology, Hematology, Medical University of Białystok, Poland.
Andrzej KołtanDepartment of Pediatrics, Hematology and Oncology, Collegium Medicum of Bydgoszcz, Poland.
Grażyna KarolczykDepartment of Pediatric Oncology and Hematology, Children's Hospital, Kielce, Poland.
Katarzyna MachnikDepartment of Pediatric Hematology and Oncology, Center of Pediatrics and Oncology, Chorzów, Poland.
Tomasz UrasińskiDepartment of Pediatrics, Hematology and Oncology, Medical University of Szczecin, Poland.
Monika LejmanLaboratory of Genetic Diagnostics, Medical University of Lublin, Poland.
Wanda BadowskaDepartment of Hematology and Oncology, Children State Hospital, Olsztyn, Poland.
Wojciech MłynarskiDepartment of Pediatrics, Oncology and Hematology, Medical University of Łódź, Poland.
Jerzy KowalczykDepartment of Pediatric, Hematology, Oncology and Transplantology, Medical University of Lublin, Poland.
Tomasz SzczepańskiDepartment of Pediatric Hematology and Oncology, Medical University of Silesia, Katowice, Poland.
Medical University of Silesia · PLMedical University of Warsaw · PLMedical University of Lublin · PLPoznan University of Medical Sciences · PLMedical University of Białystok · PLMedical University of Lodz · PLUniversity of Szczecin · PLUniversity of Wrocław · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Flow cytometry (FCM) is a precise and well-established tool to assess the minimal residual disease (MRD) level in childhood acute lymphoblastic leukemia (ALL). It is crucial to distinguish leukemic cells from their normal counterparts; thus new markers should be evaluated, to increase the accuracy of the analysis. The expression of CD73 on blast cells was measured and compared at the day of diagnosis and at days 15 and 33 of treatment. To determine antigen expression levels, a normalized scale based on median fluorescence intensity (nMFI) was used. The study group consisted of 188 patients from the Polish Pediatric Leukemia and Lymphoma Study Group. From 177 patients with positive MRD at day 15 of treatment, in 147 (83.1%) cases an increase of CD73 expression was observed (mean increase of +17 nMFI units). In addition, an increase of CD73 expression was noted in 26 of 31 (83.9%) patients at day 33 of treatment. In turn, a decrease of CD73 expression was observed only in 13/177 (7.3%) and 1/31 (3.2%) cases at days 15 and 33 of treatment, respectively. In 17 (9.6%) patients no change in expression of CD73 between diagnosis and day 15 of treatment was observed. In the great majority of cases the expression of CD73 is not only stable but increases during the early stages of treatment, which makes it a very useful marker to be used for MRD monitoring in childhood B-cell precursor (BCP)-ALL patients.

Indexed as

acute lymphoblastic leukemiaflow cytometryminimal residual disease

Identifiers

PMID35600149
PMCPMC9115592
OpenAlexW4226021455

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.