Evidence map›Paper›PMID 24583534›Full record

ArticleBlood cancer journal2014

Incidence and prognostic significance of karyotypic subgroups in older patients with acute myeloid leukemia: the Swedish population-based experience.

V Lazarevic, A-S Hörstedt, B Johansson, P Antunovic, R Billström, A Derolf, E Hulegårdh, S Lehmann, L Möllgård, C Nilsson and 7 more

Open access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

27 citing papers in PubMed, 59 citations in OpenAlex.

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  3. Hematology reports · 2025
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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

17 authors at 9 institutions in 1 country.

V Lazarevic1] Department of Hematology and Coagulation, Skåne University Hospital, Lund, Sweden [2] Department of Hematology/Transplantation, Stem Cell Center, Lund University, Lund, Sweden.
A-S HörstedtRegional Cancer Center in South Sweden, Skåne University Hospital, Lund, Sweden.
B Johansson1] Department of Clinical Genetics, University and Regional Laboratories Region Skåne, Lund, Sweden [2] Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.
P AntunovicDepartment of Hematology, Linköping University Hospital, Linköping, Sweden.
R BillströmDepartment of Medicine, Central Hospital Skövde, Skovde, Sweden.
A DerolfHematology Center, Karolinska University Hospital, Huddinge and Stockholm, Sweden.
E HulegårdhDepartment of Medicine, Sahlgrenska University Hospital, Göteborg, Sweden.
S LehmannHematology Center, Karolinska University Hospital, Huddinge and Stockholm, Sweden.
L MöllgårdDepartment of Medicine, Sahlgrenska University Hospital, Göteborg, Sweden.
C NilssonHematology Center, Karolinska University Hospital, Huddinge and Stockholm, Sweden.
S PetersonRegional Cancer Center in South Sweden, Skåne University Hospital, Lund, Sweden.
D StockelbergDepartment of Medicine, Sahlgrenska University Hospital, Göteborg, Sweden.
B UgglaDepartment of Medicine, Örebro University Hospital, Örebro, Sweden.
L WennströmDepartment of Medicine, Sahlgrenska University Hospital, Göteborg, Sweden.
A WahlinDepartment of Radiation Sciences, Umeå University, Umeå, Sweden.
M HöglundDepartment of Hematology, Academic Hospital, Uppsala, Sweden.
G Juliusson1] Department of Hematology and Coagulation, Skåne University Hospital, Lund, Sweden [2] Department of Hematology/Transplantation, Stem Cell Center, Lund University, Lund, Sweden.
Sahlgrenska University Hospital · SEKarolinska University Hospital · SESkåne University Hospital · SELinköping University Hospital · SELund University · SEÖrebro University Hospital · SESkaraborg Hospital · SEUmeå University · SEUppsala University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Swedish population-based acute myeloid leukemia registry contains data from 3251 patients (excluding acute promyelocytic leukemia) diagnosed between 1997 and 2006. Informative cytogenetic data from 1893 patients were retrospectively added, including 1054 patients aged between 60 and 79 years. Clonal abnormalities were found in 57% of the informative karyotypes. Karyotypic patterns differed by age: t(8;21), inv(16) and t(11q23) were more common in younger patients, whereas loss of 5q, 7q and 17p, monosomal karyotype (MK) and complex karyotypes were more common in older patients. Loss of 5q, 7q and 17p often occurred together within MK. Patients with 5 chromosome abnormalities had worse overall survival than those with fewer abnormalities or normal karyotype in all age groups. Loss of 5q, 7q and/or 17p had, in contrast to MK, a further negative impact on survival. Multivariable Cox regression analyses on risk factors in patients <80 years with cytogenetic abnormalities and intensive treatment revealed that age and performance status had the most significant impact on survival (both P<0.001), followed by sex (P=0.0135) and a karyotype including -7/del(7q) (P=0.048).

Identifiers

PMID24583534
PMCPMC3944658
OpenAlexW2098355123

What OpenQuestion holds

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LicenceCC BY-NC-SA
Read underepoch 390

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.