Evidence map›Paper›PMID 26379151›Full record

ArticleThe American journal of surgical pathology2016

Morphologic Features of ALK-negative Anaplastic Large Cell Lymphomas With DUSP22 Rearrangements.

Rebecca L King, Linda N Dao, Ellen D McPhail, Elaine S Jaffe, Jonathan Said, Steven H Swerdlow, Christopher A Sattler, Rhett P Ketterling, Jagmohan S Sidhu, Eric D Hsi and 9 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in The American journal of surgical pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
6.9field-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.

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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 118 citations in OpenAlex.

  1. A genetic profiling guideline to support diagnosis and clinical management of lymphomas.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Guideline
  2. Haematologica · 2019
    Trial
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Haematologica · 2023
    Article
  10. Haematologica · 2023
    Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Genetic profiling and biomarkers in peripheral T-cell lymphomas: current role in the diagnostic work-up.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2022
    Review
  18. Article
  19. Review
  20. 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

19 authors at 5 institutions in 2 countries.

Rebecca L King*Department of Laboratory Medicine and Pathology ††Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN †Hematopathology Section, Laboratory of Pathology, National Cancer Institute, Bethesda, MD ‡Department of Pathology, David Geffen School of Medicine, University of California, Los Angeles, CA §Division of Hematopathology, University of Pittsburgh Medical Center, Pittsburgh, PA ∥Department of Pathology and Laboratory Medicine, United Health Services Hospitals, Johnson City/Binghamton #Department of Pathology and Laboratory Medicine, Centrex Clinical Laboratories, Utica, NY ¶Department of Clinical Pathology, Cleveland Clinic, Cleveland, OH **Department of Laboratory Medicine and Pathology, Mayo Clinic, Jacksonville, FL ‡‡Department of Pathology, Duke University, Durham, NC.
Linda N Dao
Ellen D McPhail
Elaine S Jaffe
Jonathan Said
Steven H Swerdlow
Christopher A Sattler
Rhett P Ketterling
Jagmohan S Sidhu
Eric D Hsi
Shridevi Karikehalli
Liuyan Jiang
Sarah E Gibson
Sarah L Ondrejka
Alina Nicolae
William R Macon
Surendra Dasari
Edgardo Parrilla Castellar
Andrew L Feldman
National Cancer Institute · USCleveland Clinic · USUniversity of California, Los Angeles · USUniversity of Pittsburgh Medical Center · USServices Hospital · PK

Funding

University of Pittsburgh Clinical and Translational Science InstituteUL1TR000005 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$50.8M
The Role of Monocytes in non-Hodgkin LymphomaP50CA097274 · NCI · UNIVERSITY OF IOWA · PI WEINER, GEORGE J. · 2002 to 2021
$45.7M
Mayo Clinic Center for Translational Science ActivitiesUL1TR000135 · NCATS · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 2012 to 2015
$41.2M
Lymphoma Disease Discovery and DefintionZIASC000550 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI JAFFE, ELAINE · 2009 to 2025
$16.9M
Hematopathology DiagnosisZIABC011070 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI JAFFE, ELAINE · 2009 to 2025
$14.5M
Genetic Biomarkers for Risk Assessment of Peripheral T-Cell LymphomasR01CA177734 · NCI · MAYO CLINIC ROCHESTER · PI FELDMAN, ANDREW LEWIS · 2013 to 2017
$1.6M
NCATS NIH HHS UL1 TR000005NCATS NIH HHS UL1 TR000135NCI NIH HHS P50 CA097274NCI NIH HHS P50 CA97274NCI NIH HHS R01 CA177734
6 · The paper itself

Abstract

Systemic anaplastic large cell lymphomas (ALCLs) are classified into ALK-positive and ALK-negative types. We recently reported that ALK-negative ALCLs are genetically heterogenous. The largest subset, representing 30% of cases, had rearrangements of the DUSP22 locus. These cases had favorable outcomes similar to ALK-positive ALCL, and superior to other ALK-negative ALCLs. Here, we examined the morphologic features of these cases in more detail. First, we conducted blinded review of hematoxylin and eosin slides of 108 ALCLs from our previous study, scoring cases for the presence of 3 histologic patterns and 5 cell types. Cases then were unblinded and re-reviewed to understand these features further. DUSP22-rearranged ALCLs were more likely than other ALK-negative ALCLs to have so-called doughnut cells (23% vs. 5%; P=0.039), less likely to have pleomorphic cells (23% vs. 49%; P=0.042), and nearly always (95%) had areas with sheet-like growth (common pattern). To examine the reproducibility of these findings, we conducted blinded review of hematoxylin and eosin slides of 46 additional ALK-negative ALCLs using a 0 to 3 scoring system to predict likelihood of DUSP22 rearrangement, the results of which correlated strongly with subsequent findings by fluorescence in situ hybridization (P<0.0001). Although all ALCLs share certain morphologic features, ALCLs with DUSP22 rearrangements show significant differences from other ALK-negative ALCLs, typically showing sheets of hallmark cells with doughnut cells and few large pleomorphic cells. These morphologic findings and our previous outcome data suggest that ALK-positive ALCLs and DUSP22-rearranged ALCLs represent prototypical ALCLs, whereas ALCLs lacking rearrangements of both DUSP22 and ALK require further study.

Indexed as

Gene RearrangementAdolescentAdultAgedAnaplastic Lymphoma KinaseBiomarkers, TumorBiopsyChildDual-Specificity PhosphatasesFemaleGenetic Predisposition to DiseaseHumansImmunohistochemistryIn Situ Hybridization, FluorescenceLymphoma, Large-Cell, AnaplasticMaleALK protein, humanAnaplastic Lymphoma KinaseBiomarkers, TumorDual-Specificity PhosphatasesDUSP22 protein, humanMitogen-Activated Protein Kinase PhosphatasesReceptor Protein-Tyrosine Kinases

Identifiers

PMID26379151
PMCPMC4834837
OpenAlexW2343167150

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.