Evidence map›Paper›PMID 30117174›Full record

ArticleAmerican journal of hematology2018

Genomic and clinical characterization of B/T mixed phenotype acute leukemia reveals recurrent features and T-ALL like mutations.

Xiaoli Mi, Gabriel Griffin, Winston Lee, Sanjay Patel, Robert Ohgami, Chi Young Ok, Sa Wang, Julia T Geyer, Wenbin Xiao, Mikhail Roshal and 6 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in American journal of hematology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.7field-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

25 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. How to think about acute leukemia of ambiguous lineage.Hematology. American Society of Hematology. Education Program · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Genomic Landscape of Mixed-Phenotype Acute Leukemia.International journal of molecular sciences · 2022
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Observational
  18. Article
  19. Review
  20. TCRCell · 2021
    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 6 institutions in 1 country.

Xiaoli MiHarvard-MIT Division of Health Sciences and Technology, Harvard Medical School, Boston, Massachusetts.
Gabriel GriffinDepartment of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.
Winston LeeDepartment of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.
Sanjay PatelDepartment of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.
Robert OhgamiDepartment of Pathology, Stanford University Medical Center, California.
Chi Young OkDepartment of Hematopathology, Division of Pathology and Laboratory Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Sa WangDepartment of Hematopathology, Division of Pathology and Laboratory Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Julia T GeyerDivision of Hematopathology, New York-Presbyterian/Weill Cornell Medical College, New York, New York.ORCID 0000-0002-4424-6139
Wenbin XiaoHematopathology Service, Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Mikhail RoshalHematopathology Service, Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Jacqueline S GarciaDepartment of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.
Lewis B SilvermanDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Stephen E SallanDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Jon C AsterDepartment of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.
Marian H HarrisDepartment of Pathology, Boston Children's Hospital, Boston, Massachusetts.
Olga K WeinbergDepartment of Pathology, Boston Children's Hospital, Boston, Massachusetts.ORCID 0000-0002-4250-3891
Boston Children's Hospital · USBrigham and Women's Hospital · USMemorial Sloan Kettering Cancer Center · USThe University of Texas MD Anderson Cancer Center · USNewYork–Presbyterian Hospital · USStanford Medicine · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

The B/T subtype of mixed phenotype acute leukemia (B/T MPAL) is defined by co-expression of antigens of both B- and T-cell lineages on leukemic blasts. Although it has been suggested that multilineage antigen expression portends poor response to chemotherapy, the clinical characteristics and driver mutations that underlie the pathogenesis of this rare subtype of acute leukemia are scarcely known. We identified nine cases of B/T MPAL from multiple institutions and correlated clinical and immunophenotypic findings with next-generation sequencing data. We report that B/T MPAL commonly presents with lymphadenopathy in adolescence and young adulthood. While the tumors have diverse cytogenetic and genomic perturbations, recurrent acquired aberrations include mutations in the putative transcriptional regulator PHF6 and the JAK-STAT and Ras signaling pathways. Alterations were also identified in genes encoding hematopoietic transcription factors, cell cycle regulators/tumor suppressors, and chromatin modifying enzymes. The genomic landscape of B/T MPAL strongly resembles that of T-ALL subgroups associated with early developmental arrest, while genetic alterations that are common in B-ALL were rarely seen. Two-thirds of the patients responded to ALL-based chemotherapy with or without stem cell transplantation. Our observations lay the groundwork for further study of the unique biology and clinical trajectory of B/T MPAL.

Indexed as

Leukemia, Biphenotypic, AcuteMutationAdolescentAdultDrug TherapyFemaleGenomicsHematopoietic Stem Cell TransplantationHigh-Throughput Nucleotide SequencingHumansImmunophenotypingMaleMiddle AgedPrecursor T-Cell Lymphoblastic Leukemia-LymphomaYoung Adult

Identifiers

PMID30117174
PMCPMC8193761
OpenAlexW2886261415

What OpenQuestion holds

Textmetadata
LicenceTDM
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.