Evidence map›Paper›PMID 19125300›Full record

ReviewJournal of cancer research and clinical oncology2009

Clinical implications of molecular genetic aberrations in acute myeloid leukemia.

Sebastian Scholl, Hans-Joerg Fricke, Herbert G Sayer, Klaus Höffken

Abstract readReview
In one paragraph

Review in Journal of cancer research and clinical oncology, 2009. 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
–field-weighted citation impact
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.

  1. Trial
  2. Article
  3. Article
  4. Prevalence and Prognostic Value of IDH1 R132 Mutation in Newly Diagnosed AML Egyptian Patients with Normal Karyotype.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2017
    Article
  5. Review
  6. Prognostic significance of theMolecular and clinical oncology · 2015
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Biology, risk stratification, and therapy of pediatric acute leukemias: an update.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2011
    Review
  12. CREB and leukemogenesis.Critical reviews in oncogenesis · 2011
    Review
  13. Article
  14. Acute erythroid leukemia as defined in the World Health Organization classification is a rare and pathogenetically heterogeneous disease.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2010
    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

4 authors.

Sebastian SchollDepartment of Internal Medicine II, Universitätsklinikum, Jena, Germany. sebastian.scholl@med.uni-jena.de
Hans-Joerg Fricke
Herbert G Sayer
Klaus Höffken

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of different cytogenetic changes has been extensively evaluated in patients with acute myeloid leukemia (AML), and cytogenetic analysis of AML blasts is essential to form prognostic subgroups in order to stratify for the extent of therapy. Nevertheless, 40-45% of AML patients lack such cytogenetic markers, i.e., cytogenetically normal AML (CN-AML). In the past decade, different molecular aberrations were identified in AML and especially CN-AML can now be discriminated into certain prognostic subgroups. This review considers the latest advances to define the prognostic impact of molecular aberrations in AML and gives insights how such molecular markers can be applied for analysis of minimal residual disease. Furthermore, therapeutic implications as well as the potential role of new methodological techniques in analyzing expression patterns of AML blasts are discussed.

Indexed as

Chromosome AberrationsCCAAT-Enhancer-Binding Proteinsfms-Like Tyrosine Kinase 3Gene DuplicationGene FrequencyHumansLeukemia, Myeloid, AcuteMolecular BiologyNeoplasm ProteinsPrognosisProtein-Tyrosine KinasesSurvival AnalysisWT1 ProteinsBAALC protein, humanCCAAT-Enhancer-Binding ProteinsCEBPA protein, humanFLT3 protein, humanfms-Like Tyrosine Kinase 3Neoplasm ProteinsProtein-Tyrosine KinasesWT1 Proteins

Identifiers

PMID19125300
PMCPMC12160160

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.