Evidence map›Paper›PMID 37439336›Full record

ReviewHaematologica2023

Down syndrome and leukemia: from basic mechanisms to clinical advances.

André Baruchel, Jean-Pierre Bourquin, John Crispino, Sergi Cuartero, Henrik Hasle, Johann Hitzler, Jan-Henning Klusmann, Shai Izraeli, Andrew A Lane, Sébastien Malinge and 5 more

Open access · goldAbstract readReview
In one paragraph

Review in Haematologica, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 2 pooled it
13.1field-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

35 citing papers in PubMed, 2 syntheses or guidelines pooled it, 45 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

15 authors at 15 institutions in 10 countries.

André BaruchelHôpital Universitaire Robert Debré (APHP and Université Paris Cité), Paris.
Jean-Pierre BourquinUniversity Children's Hospital, Zurich.
John CrispinoSt. Jude Children's Research Hospital, Memphis, TN.
Sergi CuarteroJosep Carreras Leukemia Research Institute, Barcelona. scuartero@carrerasresearch.org.
Henrik HasleDepartment of Pediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark.
Johann HitzlerThe Hospital for Sick Children, Toronto.
Jan-Henning KlusmannDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt.
Shai IzraeliSchneider Children's Medical Center of Israel, Petah Tikva, Israel; Dept. of Human Molecular Genetics and Biochemistry, Sackler School of Medicine, Aviv University.
Andrew A LaneDana-Farber Cancer Institute, Boston, MA.
Sébastien MalingeTelethon Kids Institute - Cancer Centre, Perth. sebastien.malinge@telethonkids.org.au.
Karen R RabinBaylor College of Medicine, Texas Children's Cancer Center, Houston, TX.
Irene RobertsUniversity of Oxford, Oxford.
Sandra RyeomDepartment of Surgery, Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY.
Sarah K TasianChildren's Hospital of Philadelphia and University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.
Elvin WagenblastIcahn School of Medicine at Mount Sinai, New York, NY; USA.
Aarhus University Hospital · DKBaylor College of Medicine · USChildren's Hospital of Philadelphia · USColumbia University Irving Medical Center · USDana-Farber Cancer Institute · USGoethe University Frankfurt · DEHôpital Robert-Debré · FRHospital for Sick Children · CAIcahn School of Medicine at Mount Sinai · USJosep Carreras Leukaemia Research Institute · ESSt. Jude Children's Research Hospital · USTel Aviv University · ILThe Kids Research Institute Australia · AUUniversity Children's Hospital Zurich · CHUniversity of Oxford · GB

Funding

Multispecific targeting incorporating cytokine receptor pathways in high risk pediatric acute leukemias to improve durability of adoptive cell therapy-induced remissionsU01CA232486 · NCI · UNIVERSITY OF COLORADO DENVER · PI FRY, TERRY J., TASIAN, SARAH KATHLEEN · 2018 to 2018
$4.0M
Negative Regulation of VEGF-Mediated AngiogenesisR01CA118374 · NCI · UNIVERSITY OF PENNSYLVANIA · PI RYEOM, SANDRA · 2009 to 2019
$3.4M
Towards rational design of combination therapeutic targetsU01CA243072 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI TAN, KAI, TASIAN, SARAH KATHLEEN · 2020 to 2024
$2.6M
NCI NIH HHS R01 CA118374NCI NIH HHS U01 CA232486NCI NIH HHS U01 CA243072
6 · The paper itself

Abstract

Children with Down syndrome (DS, trisomy 21) are at a significantly higher risk of developing acute leukemia compared to the overall population. Many studies investigating the link between trisomy 21 and leukemia initiation and progression have been conducted over the last two decades. Despite improved treatment regimens and significant progress in iden - tifying genes on chromosome 21 and the mechanisms by which they drive leukemogenesis, there is still much that is unknown. A focused group of scientists and clinicians with expertise in leukemia and DS met in October 2022 at the Jérôme Lejeune Foundation in Paris, France for the 1st International Symposium on Down Syndrome and Leukemia. This meeting was held to discuss the most recent advances in treatment regimens and the biology underlying the initiation, progression, and relapse of acute lymphoblastic leukemia and acute myeloid leukemia in children with DS. This review provides a summary of what is known in the field, challenges in the management of DS patients with leukemia, and key questions in the field.

Indexed as

Down SyndromeLeukemia, Myeloid, AcutePrecursor Cell Lymphoblastic Leukemia-LymphomaAcute DiseaseChildFranceHumans

Identifiers

PMID37439336
PMCPMC10542835
OpenAlexW4384120739

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.