Evidence map›Paper›PMID 28708320›Full record

SynthesisPediatric blood & cancer2017

Monosomy 7/del (7q) in inherited bone marrow failure syndromes: A systematic review.

Alex Pezeshki, Shreya Podder, Ralph Kamel, Seth J Corey

Abstract readSystematic Review
In one paragraph

Synthesis in Pediatric blood & cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Observational
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Aplastic Anemia.The New England journal of medicine · 2018
    Review
  14. 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

4 authors at 2 institutions in 1 country.

Alex PezeshkiWayne State University School of Medicine, Detroit, Michigan.
Shreya PodderDivision of Pediatric Hematology, Oncology, and Stem Cell Transplantation, Children's Hospital of Richmond and Massey Cancer Center, Virginia Commonwealth University School of Medicine, Richmond, Virginia.
Ralph KamelDivision of Pediatric Hematology, Oncology, and Stem Cell Transplantation, Children's Hospital of Richmond and Massey Cancer Center, Virginia Commonwealth University School of Medicine, Richmond, Virginia.
Seth J CoreyDivision of Pediatric Hematology, Oncology, and Stem Cell Transplantation, Children's Hospital of Richmond and Massey Cancer Center, Virginia Commonwealth University School of Medicine, Richmond, Virginia.ORCID http://orcid.org/0000-0002-6704-4142
Virginia Commonwealth University · USWayne State University · US

Funding

Multiscale Modeling of Myelodysplastic SyndromesR01HL128173 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI COREY, SETH JOEL, KIMMEL, MAREK · 2015 to 2019
$3.8M
Genetic Modifiers for Cancer Stem Cells in Secondary MDS/AMLR21CA159203 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI COREY, SETH JOEL · 2014 to 2015
$374k
NCI NIH HHS R21 CA159203NHLBI NIH HHS R01 HL128173
6 · The paper itself

Abstract

Inherited bone marrow failure syndromes (IBMFS) are rare cancer predisposition syndromes with an especially high risk of transformation to myelodysplastic syndrome (MDS) and/or acute myeloid leukemia (AML). We performed a retrospective systematic review of reported MDS/AML arising in the eight most common IBMFS to determine the frequency and outcome of chromosome 7 abnormalities. We identified 738 MDS/AML cases of 4,293 individuals. Monosomy 7 or del (7q) occurred in ∼17%. Greater understanding of the roles played by sequential acquisition of genetic and cytogenetic changes will provide insights into myeloid leukemogenesis and improve the surveillance and hopefully outcomes for individuals with IBMFS.

Indexed as

Chromosome DeletionAdolescentAdultAnemia, AplasticBone Marrow DiseasesBone Marrow Failure DisordersChildChild, PreschoolChromosomes, Human, Pair 7Hemoglobinuria, ParoxysmalHumansInfantInfant, NewbornRetrospective StudiesYoung Adultacute myeloid leukemiabone marrow failure syndromesmonosomy 7

Identifiers

PMID28708320
PMCPMC5937691
OpenAlexW2734528534

What OpenQuestion holds

Textmetadata
LicenceTDM
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.