Evidence map›Paper›PMID 33558656›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2021

Myelodysplastic syndrome with t(6;9)(p22;q34.1)/DEK-NUP214 better classified as acute myeloid leukemia? A multicenter study of 107 cases.

Hong Fang, Mariko Yabe, Xiaohui Zhang, Young Kim, Xiaojun Wu, Peng Wei, Sunyi Chi, Lan Zheng, Guillermo Garcia-Manero, Lina Shao and 12 more

Open access · bronzeAbstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2021. 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
2.3field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Acute myeloid leukemia withThe Journal of international medical research · 2025
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Myelodysplastic Syndrome: Diagnosis and Screening.Diagnostics (Basel, Switzerland) · 2022
    Review
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

22 authors at 10 institutions in 1 country.

Hong FangDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0003-1780-5959
Mariko YabeDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Xiaohui ZhangDepartment of Pathology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Young KimDepartment of Pathology, City of Hope National Medical Center, Duarte, CA, USA.ORCID http://orcid.org/0000-0003-4491-0033
Xiaojun WuDepartment of Pathology, John Hopkins University, Baltimore, MD, USA.
Peng WeiDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0001-7758-6116
Sunyi ChiDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Lan ZhengDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Guillermo Garcia-ManeroDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0002-3631-2482
Lina ShaoDepartment of Pathology, The University of Michigan Medical Center, Ann Arbor, MI, USA.
Ji YuanDepartment of Pathology, University of Nebraska Medical Center, Omaha, NE, USA.
Yulei ShenDepartment of Pathology, The University of Michigan Medical Center, Ann Arbor, MI, USA.
Gang ZhengDepartment of Pathology, John Hopkins University, Baltimore, MD, USA.ORCID http://orcid.org/0000-0003-0276-9430
Guiling TangDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Wei WangDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Sanam LoghaviDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0001-8980-3202
Qi ShenDepartment of Pathology, Advent Health-Orlando, Orlando, FL, USA.
Yongzhong YuanDepartment of Pathology, University of Arkansas for Medical Sciences, Little Rock, AK, USA.
Rong HeDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0001-6116-8163
Dong ChenDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
L Jeffrey MedeirosDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0001-6577-8006
Shimin HuDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. shu1@mdanderson.org.ORCID http://orcid.org/0000-0001-7110-3814
The University of Texas MD Anderson Cancer Center · USJohns Hopkins University · USMayo Clinic in Arizona · USUniversity of Michigan · USAdventHealth Orlando · USCity Of Hope National Medical Center · USMemorial Sloan Kettering Cancer Center · USMoffitt Cancer Center · USUniversity of Arkansas for Medical Sciences · USUniversity of Nebraska Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

t(6;9)(p22;q34.1)/DEK-NUP214 is a recurrent genetic abnormality that occurs in 1-2% of patients with acute myeloid leukemia (AML), and rarely in myelodysplastic syndrome (MDS). It has been suggested by others that all myeloid neoplasms with t(6;9)/DEK-NUP214 may be considered as AML, even when blast count is <20%. In this study, we compared the clinicopathologic features of 107 patients with myeloid neoplasms harboring t(6;9)/DEK-NUP214: 33 MDS and 74 AML. Compared with patients with AML, patients with MDS were older (p = 0.10), had a lower white blood cell count (p = 0.0017), a lower blast count in the peripheral blood (p < 0.0001) and bone marrow (p < 0.0001), a higher platelet count (p = 0.022), and a lower frequency of FLT3-ITD mutation (p = 0.01). In addition, basophilia was not a common feature in the patients of this cohort. Although there was no difference in overall survival between MDS and AML patients (p = 0.18) in the entire cohort, the survival curves did show a trend toward favorable survival in MDS patients. Multivariate analyses showed that initial diagnosis of MDS vs. AML and allogeneic hematopoietic stem cell transplantation were prognostic factors for survival of patients with t(6;9)/DEK-NUP214 (p = 0.008 and p < 0.0001, respectively). Our data suggest that MDS with t(6;9)/DEK-NUP214 is prognostically not equivalent to AML with t(6;9)/DEK-NUP214. These data also show that stem cell transplantation greatly improves the survival of MDS and AML patients with myeloid neoplasms associated with t(6;9)/DEK-NUP214.

Indexed as

AdolescentAdultAgedAged, 80 and overChildChromosomal Proteins, Non-HistoneChromosomes, Human, Pair 6Chromosomes, Human, Pair 9FemaleHumansLeukemia, Myeloid, AcuteMaleMiddle AgedMyelodysplastic SyndromesNuclear Pore Complex ProteinsOncogene FusionChromosomal Proteins, Non-HistoneDEK protein, humanNuclear Pore Complex ProteinsNUP214 protein, humanOncogene ProteinsOncogene Proteins, FusionPoly-ADP-Ribose Binding Proteins

Identifiers

PMID33558656
OpenAlexW3127759772

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.