Evidence map›Paper›PMID 28495918›Full record

ArticleHaematologica2017

Bone marrow morphology is a strong discriminator between chronic eosinophilic leukemia, not otherwise specified and reactive idiopathic hypereosinophilic syndrome.

Sa A Wang, Robert P Hasserjian, Wayne Tam, Albert G Tsai, Julia T Geyer, Tracy I George, Kathryn Foucar, Heesun J Rogers, Eric D Hsi, Bryan A Rea and 5 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
5.5field-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

21 citing papers in PubMed, 76 citations in OpenAlex.

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  14. Myeloid/lymphoid neoplasms with FLT3 rearrangement.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2021
    Article
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  17. Article
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  19. Hematopoietic neoplasms with 9p24/JAK2 rearrangement: a multicenter study.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2019
    Article
  20. B-ALL With t(5;14)(q31;q32);Frontiers in oncology · 2019
    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

15 authors at 8 institutions in 1 country.

Sa A WangDepartment of Hematopathology, M.D. Anderson Cancer Center, Houston, TX, USA swang5@mdanderson.org.
Robert P HasserjianDepartment of Pathology, Massachusetts General Hospital, Boston, MA, USA.
Wayne TamDepartment of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY.
Albert G TsaiDepartment of Pathology, Stanford University, CA, USA.
Julia T GeyerDepartment of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY.
Tracy I GeorgeDepartment of Pathology, University of New Mexico, Albuquerque, NM, USA.
Kathryn FoucarDepartment of Pathology, University of New Mexico, Albuquerque, NM, USA.
Heesun J RogersDepartment of Laboratory Medicine, Cleveland Clinic, OH, USA.
Eric D HsiDepartment of Laboratory Medicine, Cleveland Clinic, OH, USA.
Bryan A ReaDepartment of Pathology and Laboratory Medicine, the University of Pennsylvania, Philadelphia, PA, USA.
Adam BaggDepartment of Pathology and Laboratory Medicine, the University of Pennsylvania, Philadelphia, PA, USA.
Carlos E Bueso-RamosDepartment of Hematopathology, M.D. Anderson Cancer Center, Houston, TX, USA.
Daniel A ArberDepartment of Pathology and Laboratory Medicine, University of Chicago, IL, USA.
Srdan VerstovsekDepartment of Leukemia, M.D. Anderson Cancer Center, Houston, TX, USA.
Attilio OraziDepartment of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY.
Cornell University · USThe University of Texas MD Anderson Cancer Center · USCleveland Clinic · USUniversity of New Mexico · USUniversity of Pennsylvania · USMassachusetts General Hospital · USStanford University · USUniversity of Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic eosinophilic leukemia, not otherwise specified can be difficult to distinguish from idiopathic hypereosinophilic syndrome according to the current World Health Organization guideline. To examine whether the morphological features of bone marrow might aid in the differential diagnosis of these two entities, we studied a total of 139 patients with a diagnosis of chronic eosinophilic leukemia, not otherwise specified (n=17) or idiopathic hypereosinophilic syndrome (n=122). As a group, abnormal bone marrow morphological features, resembling myelodysplastic syndromes, myeloproliferative neoplasm or myelodysplastic/myeloproliferative neoplasm, were identified in 40/139 (27%) patients: 16 (94%) of those with chronic eosinophilic leukemia and 24 (20%) of those with hypereosinophilic syndrome. Abnormal bone marrow correlated with older age (

Indexed as

AdolescentAdultAgedAged, 80 and overBone MarrowDiagnosis, DifferentialHumansHypereosinophilic SyndromeLeukemiaMiddle AgedMutationMyelodysplastic SyndromesMyeloproliferative DisordersYoung Adult

Identifiers

PMID28495918
PMCPMC5541870
OpenAlexW2613258404

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.