Evidence map›Paper›PMID 36169717›Full record

ArticleJournal of cancer research and clinical oncology2023

One-point flow cytometric MRD measurement to identify children with excellent outcome after intermediate-risk BCP-ALL: results of the ALL-MB 2008 study.

Alexander Popov, Guenter Henze, Julia Roumiantseva, Oleg Budanov, Mikhail Belevtsev, Tatiana Verzhbitskaya, Elena Boyakova, Liudmila Movchan, Grigory Tsaur, Maria Fadeeva and 12 more

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2023. 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
2.8field-weighted citation impact, top 10% 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, 14 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
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

22 authors at 7 institutions in 3 countries.

Alexander Popov *National Research and Clinical Center for Pediatric Hematology, Oncology and Immunology, 1, S. Mashela st, Moscow, 117998, Russian Federation. uralcytometry@gmail.com.
Guenter Henze *Department of Pediatric Oncology Hematology, Charité Universitätsmedizin Berlin, Berlin, Germany.
Julia RoumiantsevaNational Research and Clinical Center for Pediatric Hematology, Oncology and Immunology, 1, S. Mashela st, Moscow, 117998, Russian Federation.
Oleg BudanovNational Research and Clinical Center for Pediatric Hematology, Oncology and Immunology, 1, S. Mashela st, Moscow, 117998, Russian Federation.
Mikhail BelevtsevBelarussian Research Center for Pediatric Oncology, Hematology and Immunology, Minsk, Belarus.
Tatiana VerzhbitskayaRegional Children's Hospital, Ekaterinburg, Russian Federation.
Elena BoyakovaMoscow City Blood Center Named After OK Gavrilov, Moscow, Russian Federation.
Liudmila MovchanBelarussian Research Center for Pediatric Oncology, Hematology and Immunology, Minsk, Belarus.
Grigory TsaurRegional Children's Hospital, Ekaterinburg, Russian Federation.
Maria FadeevaNational Research and Clinical Center for Pediatric Hematology, Oncology and Immunology, 1, S. Mashela st, Moscow, 117998, Russian Federation.
Svetlana LagoykoNational Research and Clinical Center for Pediatric Hematology, Oncology and Immunology, 1, S. Mashela st, Moscow, 117998, Russian Federation.
Liudmila ZharikovaNational Research and Clinical Center for Pediatric Hematology, Oncology and Immunology, 1, S. Mashela st, Moscow, 117998, Russian Federation.
Natalia MiakovaNational Research and Clinical Center for Pediatric Hematology, Oncology and Immunology, 1, S. Mashela st, Moscow, 117998, Russian Federation.
Dmitry LitvinovNational Research and Clinical Center for Pediatric Hematology, Oncology and Immunology, 1, S. Mashela st, Moscow, 117998, Russian Federation.
Olga KhlebnikovaRegional Children's Hospital, Ekaterinburg, Russian Federation.
Olga StrenevaRegional Children's Hospital, Ekaterinburg, Russian Federation.
Elena StolyarovaBelarussian Research Center for Pediatric Oncology, Hematology and Immunology, Minsk, Belarus.
Natalia PonomarevaRepublican Children's Hospital, Moscow, Russian Federation.
Galina NovichkovaNational Research and Clinical Center for Pediatric Hematology, Oncology and Immunology, 1, S. Mashela st, Moscow, 117998, Russian Federation.
Larisa FechinaRegional Children's Hospital, Ekaterinburg, Russian Federation.
Olga AleinikovaNational Research and Clinical Center for Pediatric Hematology, Oncology and Immunology, 1, S. Mashela st, Moscow, 117998, Russian Federation.
Alexander KarachunskiyNational Research and Clinical Center for Pediatric Hematology, Oncology and Immunology, 1, S. Mashela st, Moscow, 117998, Russian Federation.
Federal State Institution Hematology Research Center · RUBelarusian Research Center For Pediatric Oncology and Hematology · BYRegional Children's Clinical Hospital No. 1 · RUInstitute of Medical Cell Technologies · RUCharité - Universitätsmedizin Berlin · DECity Clinical Hospital · RURussian Children's Clinical Hospital · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMeasurement of minimal residual disease (MRD) with multicolor flow cytometry (MFC) has become an important tool in childhood acute lymphoblastic leukemia (ALL), mainly to identify rapid responders and reduce their therapy intensity. Protocols of the Moscow-Berlin (MB) group use a comparatively low (for standard risk; SR) or moderate (for intermediate risk; ImR) treatment intensity from the onset, based on initial patient characteristics. Recently, we reported that 90% of SR patients-50% B cell precursor (BCP-ALL)-MFC-MRD negative at end of induction (EOI)-had 95% event-free survival (EFS). 

methodsIn the present study, we applied this method to children with initial ImR features.

resultsIn study MB 2008, 1105 children-32% of BCP-ALL patients-were assigned to the ImR group. Of these, 227 were treated in clinics affiliated with MFC laboratories of the MB group network, and included in this MFC-MRD pilot study. A single-point MFC-MRD measurement at the EOI with the threshold of 0.01% identified 65% of patients-20% of all BCP-ALL patients-with EFS of 93.5%.

conclusionTaking both studies together, the combination of clinical parameters and a one-point MRD measurement identifies 70% of BCP-ALL patients with an excellent outcome after low- or moderate-intensity therapy and avoids overtreatment of a significant proportion of patients.

Indexed as

Neoplasm, ResidualBerlinChildFlow CytometryHumansMoscowPilot ProjectsIntermediate-risk acute lymphoblastic leukemiaMinimal residual diseaseReduced-intensity treatment

Identifiers

PMID36169717
PMCPMC11797682
OpenAlexW4297458882

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.