Evidence map›Paper›PMID 29090343›Full record

Trial reportAnnals of hematology2017

Epidemiological, genetic, and clinical characterization by age of newly diagnosed acute myeloid leukemia based on an academic population-based registry study (AMLSG BiO).

Gabriele Nagel, D Weber, E Fromm, S Erhardt, M Lübbert, W Fiedler, T Kindler, J Krauter, P Brossart, A Kündgen and 24 more

Registry-linked trialOpen access · hybridAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Annals of hematology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01252485 (Registry Study on Patient Characteristics, Biological Disease Profile and Clinical Outcome in Acute Myeloid Leukemia and Related Neoplasms - The Biology and Outcome), which is not on this map. Cited by 95 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed, 3 pooled it
8.1field-weighted citation impact, top 2% 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.

NCT01252485 recruitingnot on this map

Registry Study on Patient Characteristics, Biological Disease Profile and Clinical Outcome in Acute Myeloid Leukemia and Related Neoplasms - The Biology and Outcome (BiO)-Project

TypeobservationalSponsorUniversity of UlmRan2010 to 2044Enrolled50,000ConditionsAcute Myeloid Leukemia (AML), MDS/AML
3 · Its place in the literature

Who cites it

95 citing papers in PubMed, 3 syntheses or guidelines pooled it, 168 citations in OpenAlex.

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  15. Gemtuzumab Ozogamicin inJournal of clinical oncology : official journal of the American Society of Clinical Oncology · 2020
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35 more citing papers are in PubMed but not listed here.

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

34 authors at 18 institutions in 2 countries.

Gabriele NagelInstitute of Epidemiology and Medical Biometry, Ulm University, Helmholtzstr. 22, 89081, Ulm, Germany. gabriele.nagel@uni-ulm.de.
D WeberDepartment of Internal Medicine III, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
E FrommInstitute of Epidemiology and Medical Biometry, Ulm University, Helmholtzstr. 22, 89081, Ulm, Germany.
S ErhardtInstitute of Epidemiology and Medical Biometry, Ulm University, Helmholtzstr. 22, 89081, Ulm, Germany.
M LübbertDepartment of Internal Medicine I, Faculty of Medicine, University Hospital Freiburg, Freiburg, Germany.
W FiedlerDepartment of Internal Medicine II, University Hospital Hamburg-Eppendorf, Hamburg, Germany.
T KindlerDepartment of Internal Medicine III, University Medical Center Mainz, Mainz, Germany.
J KrauterDepartment of Internal Medicine III, Hospital Braunschweig, Braunschweig, Germany.
P BrossartDepartment of Internal Medicine III, University Hospital of Bonn, Bonn, Germany.
A KündgenDepartment of Hematology, Oncology and Clinical Immunology, University Hospital of Düsseldorf, Düsseldorf, Germany.
H R SalihDepartment of Internal Medicine II, University Hospital of Tübingen, Tübingen, Germany.
J WestermannDepartment of Hematology, Oncology and Tumor Immunology, Charité - Campus Virchow Clinic, Berlin, Germany.
G WulfDepartment of Hematology and Oncology, University Hospital of Göttingen, Göttingen, Germany.
B HertensteinDepartment of Internal Medicine I, Hospital Bremen-Mitte, Bremen, Germany.
M WattadDepartment of Hematology and Oncology, Hospital Essen-Werden, Essen, Germany.
K GötzeDepartment of Internal Medicine III, University Hospital Klinikum rechts der Isar, Munich, Germany.
D KraemerDepartment of Oncology and Hematology, Hospital Oldenburg, Oldenburg, Germany.
T HeinickeDepartment of Hematology and Oncology, University Hospital of Magdeburg, Magdeburg, Germany.
M GirschikofskyDepartment of Hematology and Oncology, Hospital Elisabethinen Linz, Linz, Austria.
H G DerigsDepartment of Internal Medicine III, Hospital Frankfurt-Hoechst, Frankfurt, Germany.
H A HorstDepartment of Internal Medicine II, University Hospital of Schleswig-Holstein, Kiel, Germany.
C RudolphDepartment of Internal Medicine III, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
M HeuserDepartment of Hematology, Hemostasis, Oncology, and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
G GöhringInstitute of Human Genetics, Hannover Medical School, Hannover, Germany.
V TeleanuDepartment of Internal Medicine III, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
L BullingerDepartment of Internal Medicine III, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
F TholDepartment of Hematology, Hemostasis, Oncology, and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
V I GaidzikDepartment of Internal Medicine III, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
P PaschkaDepartment of Internal Medicine III, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
K DöhnerDepartment of Internal Medicine III, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
A GanserDepartment of Hematology, Hemostasis, Oncology, and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
Hartmut DöhnerDepartment of Internal Medicine III, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany. hartmut.doehner@uniklinik-ulm.de.
R F SchlenkDepartment of Internal Medicine III, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
German-Austrian AML Study Group (AMLSG)
Medizinische Hochschule Hannover · DEHelmholtz-Institute Ulm · DEUniversity Hospital Ulm · DEGoethe University Frankfurt · DETUM Klinikum · DEUniversität Hamburg · DEUniversitätsmedizin Göttingen · DEUniversity Hospital Bonn · DEDüsseldorf University Hospital · DEJohannes Gutenberg University Mainz · DEKlinikum Bremen-Mitte · DEKlinikum Oldenburg · DEKrankenhaus der Elisabethinen · ATNational Center for Tumor Diseases · DEUniversität Ulm · DEUniversity Children's Hospital Tübingen · DEUniversity Hospital Schleswig-Holstein · DEUniversity Medical Center Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We describe genetic and clinical characteristics of acute myeloid leukemia (AML) patients according to age from an academic population-based registry. Adult patients with newly diagnosed AML at 63 centers in Germany and Austria were followed within the AMLSG BiO registry (NCT01252485). Between January 1, 2012, and December 31, 2014, data of 3525 patients with AML (45% women) were collected. The median age was 65 years (range 18-94). The comparison of age-specific AML incidence rates with epidemiological cancer registries revealed excellent coverage in patients < 70 years old and good coverage up to the age of 80. The distribution according to the European LeukemiaNet (ELN) risk categorization from 2010 was 20% favorable, 31% intermediate-1, 28% intermediate-2, and 21% adverse. With increasing age, the relative but not the absolute prevalence of patients with ELN favorable and intermediate-1 risk (p < 0.001), with activating FLT3 mutations (p < 0.001), with ECOG performance status < 2 (p < 0.001), and with HCT-CI comorbidity index < 3 (p < 0.001) decreased. Regarding treatment, obesity and favorable risk were associated with an intensive treatment, whereas adverse risk, higher age, and comorbidity index > 0 were associated with non-intensive treatment or best supportive care. The AMLSG BiO registry provides reliable population-based distributions of genetic, clinical, and treatment characteristics according to age.

Indexed as

fms-Like Tyrosine Kinase 3Leukemia, Myeloid, AcuteMutationRegistriesAdolescentAdultAgedAged, 80 and overAustriaFemaleGermanyHumansMaleMiddle AgedFLT3 protein, humanfms-Like Tyrosine Kinase 3AMLEpidemiologyGeneticsOlder ageRegistry

Identifiers

PMID29090343
PMCPMC5691091
OpenAlexW2766330759

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.