Evidence map›Paper›PMID 21135859›Full record

ArticleLeukemia2011

Risk stratification using a new prognostic score for patients with secondary acute myeloid leukemia: results of the prospective AML96 trial.

F Stölzel, M Pfirrmann, W E Aulitzky, M Kaufmann, H Bodenstein, M Bornhäuser, C Röllig, M Kramer, B Mohr, U Oelschlägel and 6 more

Abstract read
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In one paragraph

Article in Leukemia, 2011. 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
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  8. Identification of key pathways and genes inOncoTargets and therapy · 2018
    Article
  9. Single Nucleotide Polymorphisms inFrontiers in oncology · 2018
    Article
  10. Article
  11. Article
  12. Article
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  14. 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

16 authors.

F StölzelMedizinische Klinik und Poliklinik I, University Hospital Carl Gustav Carus Dresden, Dresden, Germany. friedrich.stoelzel@uniklinikum-dresden.de
M Pfirrmann
W E Aulitzky
M Kaufmann
H Bodenstein
M Bornhäuser
C Röllig
M Kramer
B Mohr
U Oelschlägel
N Schmitz
S Soucek
C Thiede
G Ehninger
M Schaich
Study Alliance Leukemia

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with secondary acute myeloid leukemia (sAML) are generally thought to have a poor prognosis. As there are no prognostic risk stratification models for patients with sAML available, the aim of this study was to obtain a scoring system. Prognostic factors influencing overall survival (OS) and event-free survival (EFS) were analyzed in 305 sAML patients treated in the prospective AML96 trial. The obtained prognostic scoring system was then validated in an independent patient cohort included in the AML2003 and AML60+ trials. In addition to the known risk factors for AML, age and karyotype, we identified the absolute platelet count and the Nucleophosmin 1 mutational status at diagnosis as prognostic factors of sAML patients. A pronounced distribution of sAML patients into three score groups was achieved showing a 2-year OS/EFS of 52/44% for patients in the low-risk group, 21/12% in the intermediate-risk group and 7/3% in the high-risk group (both P<0.001). Validation of this scoring system in a second independent set of sAML patients revealed similar significantly different survival results. In conclusion, for the first time, a prognostic scoring system is provided for sAML patients, allowing differential treatment strategies in the future.

Indexed as

AdultAgedAged, 80 and overClinical Trials as TopicFemaleHumansLeukemia, Myeloid, AcuteLogistic ModelsMaleMiddle AgedMutationNeoplasms, Second PrimaryNuclear ProteinsNucleophosminPlatelet CountPrognosisNPM1 protein, humanNuclear ProteinsNucleophosmin

Identifiers

PMID21135859

What OpenQuestion holds

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Registered trials

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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.