Evidence map›Paper›PMID 30504903›Full record

ArticleBone marrow transplantation2019

Clinical impact of clonal hematopoiesis in acute myeloid leukemia patients receiving allogeneic transplantation.

Juliane Grimm, Marius Bill, Madlen Jentzsch, Stefanie Beinicke, Janine Häntschel, Karoline Goldmann, Julia Schulz, Michael Cross, Georg-Nikolaus Franke, Gerhard Behre and 5 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 6% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

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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

15 authors at 1 institution in 1 country.

Juliane GrimmDepartment of Hematology and Oncology, University of Leipzig, Leipzig, Germany.
Marius BillDepartment of Hematology and Oncology, University of Leipzig, Leipzig, Germany.
Madlen JentzschDepartment of Hematology and Oncology, University of Leipzig, Leipzig, Germany.
Stefanie BeinickeDepartment of Hematology and Oncology, University of Leipzig, Leipzig, Germany.
Janine HäntschelDepartment of Hematology and Oncology, University of Leipzig, Leipzig, Germany.
Karoline GoldmannDepartment of Hematology and Oncology, University of Leipzig, Leipzig, Germany.
Julia SchulzDepartment of Hematology and Oncology, University of Leipzig, Leipzig, Germany.
Michael CrossDepartment of Hematology and Oncology, University of Leipzig, Leipzig, Germany.
Georg-Nikolaus FrankeDepartment of Hematology and Oncology, University of Leipzig, Leipzig, Germany.
Gerhard BehreDepartment of Hematology and Oncology, University of Leipzig, Leipzig, Germany.
Vladan VucinicDepartment of Hematology and Oncology, University of Leipzig, Leipzig, Germany.
Wolfram PönischDepartment of Hematology and Oncology, University of Leipzig, Leipzig, Germany.
Thoralf LangeDepartment of Hematology and Oncology, University of Leipzig, Leipzig, Germany.
Dietger NiederwieserDepartment of Hematology and Oncology, University of Leipzig, Leipzig, Germany.ORCID 0000-0002-4737-1103
Sebastian SchwindDepartment of Hematology and Oncology, University of Leipzig, Leipzig, Germany. Sebastian.Schwind@medizin.uni-leipzig.de.
University Hospital Leipzig · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Age-related somatic mutations linked to clonal hematopoiesis have been found in apparently healthy individuals and increase the risk of developing hematologic malignancies. In acute myeloid leukemia (AML) the clinical relevance of clonal hematopoiesis remains controversial and data on patients with detectable clonal hematopoiesis, consolidated with hematopoietic stem cell transplantation are limited. We analyzed samples from 113 AML patients in complete remission prior to hematopoietic stem cell transplantation for the presence of clonal hematopoiesis-associated mutations. The results were correlated with clinical and biological data. In complete remission we found 75 mutations previously linked to clonal hematopoiesis in 47 patients (41.6%). Twenty patients had ≥2 mutations linked to clonal hematopoiesis. DNMT3A, TET2, and ASXL1 were most frequently mutated. When compared to pre-treatment samples we found variable patterns of mutation persistence depending on the gene mutated. In AML patients after allogeneic hematopoietic stem cell transplantation the presence of clonal hematopoiesis-associated mutations in complete remission did not associate with inferior clinical outcome. This study demonstrates that clonal hematopoiesis is a frequent phenomenon in AML patients. Presence of clonal hematopoiesis has no negative prognostic impact in the context of an allogeneic hematopoietic stem cell transplantation and might be beneficial if certain genes are affected.

Indexed as

AdultAgedFemaleHematopoiesisHematopoietic Stem Cell TransplantationHumansLeukemia, Myeloid, AcuteMaleMiddle AgedTransplantation ConditioningTransplantation, Homologous

Identifiers

PMID30504903
OpenAlexW2902297851

What OpenQuestion holds

Textmetadata
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.