Evidence map›Paper›PMID 30603901›Full record

ArticleJournal of cancer research and clinical oncology2019

Prognostic value of initial bone marrow disease detection by multiparameter flow cytometry in children with neuroblastoma.

Alexander Popov, Alexander Druy, Egor Shorikov, Tatiana Verzhbitskaya, Alexander Solodovnikov, Leonid Saveliev, Godelieve A M Tytgat, Grigory Tsaur, Larisa Fechina

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
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

9 authors at 3 institutions in 2 countries.

Alexander PopovDmitry Rogachev National Research Center of Pediatric Hematology, Oncology and Immunology, 1, S. Mashela st, Moscow, 117997, Russian Federation. uralcytometry@gmail.com.ORCID http://orcid.org/0000-0002-0889-6986
Alexander DruyDmitry Rogachev National Research Center of Pediatric Hematology, Oncology and Immunology, 1, S. Mashela st, Moscow, 117997, Russian Federation.
Egor ShorikovPET-Technology Center of Nuclear Medicine, 29, Soboleva st, Yekaterinburg, 620905, Russian Federation.
Tatiana VerzhbitskayaResearch Institute of Medical Cell Technologies, 22A, K. Marx st, Yekaterinburg, 620026, Russian Federation.
Alexander SolodovnikovResearch Institute of Medical Cell Technologies, 22A, K. Marx st, Yekaterinburg, 620026, Russian Federation.
Leonid SavelievResearch Institute of Medical Cell Technologies, 22A, K. Marx st, Yekaterinburg, 620026, Russian Federation.
Godelieve A M TytgatDepartment of Pediatric Oncology, Emma Children's Hospital (EKZ/AMC), Meibergdreef, 1105 AZ, Amsterdam, The Netherlands.
Grigory TsaurResearch Institute of Medical Cell Technologies, 22A, K. Marx st, Yekaterinburg, 620026, Russian Federation.
Larisa FechinaResearch Institute of Medical Cell Technologies, 22A, K. Marx st, Yekaterinburg, 620026, Russian Federation.
Institute of Medical Cell Technologies · RUDmitry Rogachev National Research Center of Pediatric Hematology, Oncology and Immunology · RUEmma Kinderziekenhuis · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMulticolor flow cytometry (MFC) is widely available, fast and has an easy-to perform approach for finding neuroblastoma (NB) cells among normal bone marrow (BM) hematopoietic cells. Aim of the study was to investigate prognostic significance of initial MFC tumor cells' detection in BM of children with NB.

methods51 patients (24 boys and 27 girls) aged from 6 days to 15 years (median age 1 year 3 months) with NB were included in the study. BM samples at the time of diagnosis were obtained from 2 to 5 aspiration sites per patient. CD45(-)CD56(+)CD81(+)GD2(+)-cells were evaluated by MFC.

resultsNB cells were detected in BM by FC more frequently compared to conventional cytomorphology (49.0% and 29.4% patients, respectively, р = 0.043). Patients with NB cells detected in BM by MFC had significantly worse event-free survival and cumulative incidence of relapse/progression [0.24(0.08) and 0.60(0.10), respectively] compared to children with negative result of immunophenotyping [0.85(0.07) and 0.12(0.06), respectively, p < 0.001 in both cases]. BM involvement detection by MFC maintained its prognostic significance in various patients groups. In multivariate analysis, immunophenotyping proved to be an independent prognostic factor when analyzed jointly with other NB risk factors. In 42 patients BM involvement was also studied by RQ-PCR for PHOX2B and TH genes expression. Within groups of patients divided by RQ-PCR positivity, MFC-positivity retained prognostic significance.

conclusionsThus flow cytometric BM involvement detection has very strong prognostic impact even stronger than RQ-PCR. It could be used in combination with other parameters for the treatment strategy choice in patients with NB.

Indexed as

AdolescentAntigens, CDBiomarkers, TumorBone MarrowBone Marrow DiseasesChildChild, PreschoolFemaleFlow CytometryFollow-Up StudiesHumansImmunophenotypingInfantMaleNeuroblastomaPrognosisAntigens, CDBiomarkers, TumorBone marrowFlow cytometryNeuroblastomaPrediction of outcome

Identifiers

PMID30603901
PMCPMC11810268
OpenAlexW2906737791

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.