Evidence map›Paper›PMID 34204358›Full record

ReviewGenes2021

Cytogenetics of Pediatric Acute Myeloid Leukemia: A Review of the Current Knowledge.

Julie Quessada, Wendy Cuccuini, Paul Saultier, Marie Loosveld, Christine J Harrison, Marina Lafage-Pochitaloff

Open access · goldAbstract readReview
In one paragraph

Review in Genes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 1 pooled it
11.0field-weighted citation impact, top 1% 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

58 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 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

6 authors at 5 institutions in 2 countries.

Julie QuessadaHematological Cytogenetics Laboratory, Timone Children's Hospital, Assistance Publique-Hôpitaux de Marseille (APHM), Faculté de Médecine, Aix Marseille University, 13005 Marseille, France.ORCID 0000-0002-3219-3172
Wendy CuccuiniHematological Cytogenetics Laboratory, Saint-Louis Hospital, Assistance Publique des Hôpitaux de Paris (APHP), 75010 Paris, France.
Paul SaultierAPHM, La Timone Children's Hospital Department of Pediatric Hematology and Oncology, 13005 Marseille, France.ORCID 0000-0002-6327-0898
Marie LoosveldAix Marseille University, CNRS, INSERM, CIML, 13009 Marseille, France.
Christine J HarrisonLeukaemia Research Cytogenetics Group Translational and Clinical Research Institute, Newcastle University Centre for Cancer Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne NE1 7RU, UK.
Marina Lafage-PochitaloffHematological Cytogenetics Laboratory, Timone Children's Hospital, Assistance Publique-Hôpitaux de Marseille (APHM), Faculté de Médecine, Aix Marseille University, 13005 Marseille, France.
Centre National de la Recherche Scientifique · FRAix-Marseille Université · FRAssistance Publique – Hôpitaux de Paris · FRInserm · FRNewcastle University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pediatric acute myeloid leukemia is a rare and heterogeneous disease in relation to morphology, immunophenotyping, germline and somatic cytogenetic and genetic abnormalities. Over recent decades, outcomes have greatly improved, although survival rates remain around 70% and the relapse rate is high, at around 30%. Cytogenetics is an important factor for diagnosis and indication of prognosis. The main cytogenetic abnormalities are referenced in the current WHO classification of acute myeloid leukemia, where there is an indication for risk-adapted therapy. The aim of this article is to provide an updated review of cytogenetics in pediatric AML, describing well-known WHO entities, as well as new subgroups and germline mutations with therapeutic implications. We describe the main chromosomal abnormalities, their frequency according to age and AML subtypes, and their prognostic relevance within current therapeutic protocols. We focus on de novo AML and on cytogenetic diagnosis, including the practical difficulties encountered, based on the most recent hematological and cytogenetic recommendations.

Indexed as

Chromosome AberrationsAdolescentChildChild, PreschoolGenetic TestingHumansInfantIn Situ Hybridization, FluorescenceKaryotypingLeukemia, Myeloid, Acuteacute megakaryoblastic leukemiaacute myeloid leukemiachildren hematological malignanciescytogeneticsFISHgenomicsinfant leukemiakaryotypepediatricsrisk-adapted therapytherapeutic trials

Identifiers

PMID34204358
PMCPMC8233729
OpenAlexW3171257991

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.