Evidence map›Paper›PMID 31000771›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2019

Clinical, immunophenotypic, and genomic findings of acute undifferentiated leukemia and comparison to acute myeloid leukemia with minimal differentiation: a study from the bone marrow pathology group.

Olga K Weinberg, Robert P Hasserjian, Ezra Baraban, Chi Young Ok, Julia T Geyer, John K S S Philip, Jason H Kurzer, Heesun J Rogers, Valentina Nardi, Richard M Stone and 6 more

Open access · bronzeAbstract readComparative Study
PubMed Publisher
In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. How to think about acute leukemia of ambiguous lineage.Hematology. American Society of Hematology. Education Program · 2024
    Review
  8. Review
  9. EJHaem · 2023
    Article
  10. Review
  11. Clinical, immunophenotypic and genomic findings of NK lymphoblastic leukemia: a study from the Bone Marrow Pathology Group.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2021
    Article
  12. Article
  13. The Bone Marrow Microenvironment Mechanisms in Acute Myeloid Leukemia.Frontiers in cell and developmental biology · 2021
    Review
  14. Frontiers in oncology · 2021
    Review
  15. Chronic myeloid neoplasms harboring concomitant mutations in myeloproliferative neoplasm driver genes (JAK2/MPL/CALR) and SF3B1.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2021
    Article
  16. [Analysis of immunophenotypes and expressions of non-myeloid antigens in acute myeloid leukemia].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2020
    Article
  17. Article
  18. Review
  19. 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

16 authors at 9 institutions in 1 country.

Olga K WeinbergDepartment of Pathology, Boston Children's Hospital, Boston, MA, USA. Olga.weinberg@childrens.harvard.edu.
Robert P HasserjianDepartment of Pathology, Massachusetts General Hospital, Boston, MA, USA.
Ezra BarabanDepartment of Pathology and Laboratory Medicine, the University of Pennsylvania, Philadelphia, PA, USA.
Chi Young OkDepartments of Hematopathology, M.D. Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0002-6822-7880
Julia T GeyerDepartment of Pathology, Weill Cornell Medical College, New York, NY, USA.
John K S S PhilipDepartment of Pathology and Laboratory Medicine, University of Chicago, Chicago, IL, USA.
Jason H KurzerDepartment of Pathology, Stanford University Medical Center, Palo Alto, CA, USA.
Heesun J RogersDepartment of Laboratory Medicine, Cleveland Clinic, Cleveland, OH, USA.ORCID http://orcid.org/0000-0001-8491-224X
Valentina NardiDepartment of Pathology, Massachusetts General Hospital, Boston, MA, USA.
Richard M StoneDepartment of Medical Oncology, Dana Farber Cancer Institute, Boston, MA, USA.
Jacqueline S GarciaDepartment of Medical Oncology, Dana Farber Cancer Institute, Boston, MA, USA.
Eric D HsiDepartment of Laboratory Medicine, Cleveland Clinic, Cleveland, OH, USA.
Adam BaggDepartment of Pathology and Laboratory Medicine, the University of Pennsylvania, Philadelphia, PA, USA.
Sa A WangDepartments of Hematopathology, M.D. Anderson Cancer Center, Houston, TX, USA.
Attilio OraziDepartment of Pathology, Weill Cornell Medical College, New York, NY, USA.
Daniel A ArberDepartment of Pathology and Laboratory Medicine, University of Chicago, Chicago, IL, USA.
Cleveland Clinic · USCornell University · USDana-Farber Cancer Institute · USMassachusetts General Hospital · USThe University of Texas MD Anderson Cancer Center · USUniversity of Chicago · USUniversity of Pennsylvania · USBoston Children's Hospital · USStanford Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute undifferentiated leukemia is a rare type of acute leukemia that shows no evidence of differentiation along any lineage. Clinical, immunophenotypic and genetic data is limited and it is uncertain if acute undifferentiated leukemia is biologically distinct from acute myeloid leukemia with minimal differentiation, which also shows limited myeloid marker expression and has been reported to have a poor prognosis. We identified 92 cases initially diagnosed as acute undifferentiated leukemia or acute myeloid leukemia with minimal differentiation from pathology databases of nine academic institutions with available diagnostic flow cytometric data, cytogenetic findings, mutational and clinical data. Outcome analysis was performed using Kaplan Meier test for the 53 patients who received induction chemotherapy. Based on cytogenetic abnormalities (N = 30) or history of myelodysplastic syndrome (N = 2), 32 cases were re-classified as acute myeloid leukemia with myelodysplasia related changes. The remaining 24 acute undifferentiated leukemia patients presented with similar age, blood counts, bone marrow cellularity, and blast percentage as the remaining 30 acute myeloid leukemia with minimal differentiation patients. Compared to acute myeloid leukemia with minimal differentiation, acute undifferentiated leukemia cases were characterized by more frequent mutations in PHF6 (5/15 vs 0/19, p = 0.016) and more frequent expression of TdT on blasts (p = 0.003) while acute myeloid leukemia with minimal differentiation cases had more frequent CD123 expression (p = 0.042). Outcome data showed no difference in overall survival, relapse free survival, or rates of complete remission between acute undifferentiated leukemia and acute myeloid leukemia with minimal differentiation groups (p > 0.05). Acute myeloid leukemia with myelodysplasia-related changes patients showed shorter survival when censoring for bone marrow transplant as compared to acute undifferentiated leukemia (p = 0.03) and acute myeloid leukemia with minimal differentiation (p = 0.002). In this largest series to date, the acute undifferentiated leukemia group shows distinct characteristics from acute myeloid leukemia with minimal differentiation, including more frequent PHF6 mutations and expression of TdT.

Indexed as

AdultAgedAged, 80 and overFemaleGenotypeHumansImmunophenotypingLeukemiaLeukemia, Myeloid, AcuteMaleMiddle Aged

Identifiers

PMID31000771
OpenAlexW2936131736

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.