Evidence map›Paper›PMID 23440662›Full record

ArticleAmerican journal of hematology2013

Systemic mastocytosis with associated clonal hematological non-mast cell lineage disease: clinical significance and comparison of chomosomal abnormalities in SM and AHNMD components.

Sa A Wang, Lloyd Hutchinson, Guilin Tang, Su S Chen, Patricia M Miron, Yang O Huh, Dan M Jones, Carlos Bueso-Ramos, Srdan Verstovsek, L Jeffrey Medeiros and 1 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in American journal of hematology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.8field-weighted citation impact, top 10% 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, 86 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Diagnosing Systemic Mastocytosis: State of the Art.International journal of laboratory hematology · 2026
    Review
  5. Review
  6. Coincidence or Connection? Revisiting the Relationship Between Mastocytosis and Lymphoma.Mediterranean journal of hematology and infectious diseases · 2026
    Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Precision Medicine in Systemic Mastocytosis.Medicina (Kaunas, Lithuania) · 2021
    Review
  14. Avapritinib for Systemic Mastocytosis.Expert review of hematology · 2021
    Article
  15. Review
  16. Review
  17. A Novel PDGFRβ Rearrangement in Systemic Mastocytosis with an Associated Haematologic Neoplasm.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2020
    Article
  18. Detection of the KITModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2020
    Article
  19. Review
  20. The Spectrum of Aggressive Mastocytosis: A Workshop Report and Literature Review.Pathobiology : journal of immunopathology, molecular and cellular biology · 2020
    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

11 authors at 3 institutions in 1 country.

Sa A WangDepartment of Hematopathology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas 77030, USA. swang5@mdanderson.org
Lloyd Hutchinson
Guilin Tang
Su S Chen
Patricia M Miron
Yang O Huh
Dan M Jones
Carlos Bueso-Ramos
Srdan Verstovsek
L Jeffrey Medeiros
Roberto N Miranda
The University of Texas MD Anderson Cancer Center · USUniversity of Massachusetts Chan Medical School · USNichols College · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Kathrin Milbury · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

Some patients with systemic mastocytosis have concurrent hematological neoplasms, designated in the World Health Organization (WHO) classification as systemic mastocytosis with associated clonal hematological non-mast cell lineage disease (SM-AHNMD). In this study, we analyzed 29 patients with SM-AHNMD and compared them to 40 patients with pure SM. The AHNMDs were classified as chronic myelomonocytic leukemia (CMML) (n = 10), myelodysplastic syndrome (MDS) (n = 7), myeloproliferative neoplasms (n = 4), B-cell lymphoma/leukemia/plasma cell neoplasms (n = 7), and acute myeloid leukemia (n = 1). Patients with SM-AHNMD were older, more frequently had constitutional symptoms and hematological abnormalities, less often had skin lesions, and had an inferior overall survival compared with pure SM patients (48 months vs. not-reached, P < 0.001). Karyotypic abnormalities were detected in 9/28 (32%) patients with SM-AHNMD but not in pure SM patients (P < 0.001). Combined imaging/ fluorescence-in-situ hybridization performed in four SM-AHNMD cases revealed shared abnormal signals in mast cells and myeloid cells in two patients with SM-CMML and one patient with SM-MDS, but not in the mast cells of a case SM-associated with chronic lymphocytic leukemia with ATM-deletion. Quantitative mutation analysis showed higher levels of mutant KIT D816V in SM-CMML and SM-MDS than in pure SM (P < 0.001). Our data indicate that the SM-AHNMD category in the WHO classification is heterogeneous, including clonally related and unrelated forms of AHNMD. The presentation, treatment, and outcome of patients with SM-AHNMD is often dictated by the type of AHNMD.

Indexed as

Abnormal KaryotypeAdultAgedAge FactorsCell LineageClone CellsDNA Mutational AnalysisFemaleHematologic NeoplasmsHumansLeukemia, Myeloid, AcuteLeukemia, Myelomonocytic, ChronicLymphoma, B-CellMaleMast CellsMastocytosis, SystemicProto-Oncogene Proteins c-kit

Identifiers

PMID23440662
PMCPMC4188390
OpenAlexW2010629849

What OpenQuestion holds

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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.