Evidence map›Paper›PMID 26123119›Full record

Trial reportBritish journal of haematology2015

TP53 overexpression is an independent adverse prognostic factor in de novo myelodysplastic syndromes with fibrosis.

Sanam Loghavi, Alyaa Al-Ibraheemi, Zhuang Zuo, Guillermo Garcia-Manero, Mariko Yabe, Sa A Wang, Hagop M Kantarjian, Cameron C Yin, Roberto N Miranda, Raja Luthra and 3 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in British journal of haematology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 pooled it
3.8field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 2 syntheses or guidelines pooled it, 50 citations in OpenAlex.

  1. Guideline
  2. The cellular model for Alzheimer's disease research: PC12 cells.Frontiers in molecular neuroscience · 2022
    Pooled it
  3. Review
  4. P53 IHC Result as a Prognostic Tool in MDS.Iranian journal of pathology · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Chronic Myelomonocytic Leukemia: Hematopathology Perspective.Journal of immunotherapy and precision oncology · 2021
    Review
  10. Review
  11. International journal of molecular sciences · 2020
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Recent Updates on Chronic Myelomonocytic Leukemia.Current hematologic malignancy reports · 2018
    Review
  18. Histological evaluation of myeloproliferative neoplasms.Journal of clinical and experimental hematopathology : JCEH · 2018
    Review
  19. Article
  20. 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

13 authors at 1 institution in 1 country.

Sanam LoghaviDepartment of Hematopathology, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0001-8980-3202
Alyaa Al-IbraheemiDepartment of Hematopathology, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA.
Zhuang ZuoDepartment 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.
Mariko YabeDepartment of Hematopathology, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA.
Sa A WangDepartment of Hematopathology, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA.
Hagop M KantarjianDepartment of Leukemia, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA.
Cameron C YinDepartment of Hematopathology, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA.
Roberto N MirandaDepartment of Hematopathology, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA.
Raja LuthraDepartment of Hematopathology, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA.
L Jeffrey MedeirosDepartment of Hematopathology, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA.
Carlos E Bueso-RamosDepartment of Hematopathology, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA.
Joseph D KhouryDepartment of Hematopathology, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
NCI NIH HHS CA016672NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

Bone marrow (BM) fibrosis is associated with poor prognosis in patients with de novo myelodysplastic syndromes (MDS). TP53 mutations and TP53 (p53) overexpression in MDS are also associated with poor patient outcomes. The prevalence and significance of TP53 mutations and TP53 overexpression in MDS with fibrosis are unknown. We studied 67 patients with de novo MDS demonstrating moderate to severe reticulin fibrosis (MDS-F). Expression of TP53 was evaluated in BM core biopsy specimens using dual-colour CD34/TP53 immunohistochemistry with computer-assisted image analysis. Mutation analysis was performed using next-generation sequencing, or Sanger sequencing methods. TP53 mutations were present in 47·1% of cases. TP53 mutation was significantly associated with TP53 expression (P = 0·0294). High levels of TP53 expression (3 +  in ≥10% cells) were associated with higher BM blast counts (P = 0·0149); alterations of chromosomes 5 (P = 0·0009) or 7 (P = 0·0141); complex karyotype (P = 0·0002); high- and very-high risk IPSS-R groups (P = 0·009); and TP53 mutations (P = 0·0003). High TP53 expression independently predicted shorter overall survival (OS) by multivariate analysis (P = <0·001). Expression of TP53 by CD34-positive cells was associated with shorter OS and leukaemia-free survival (P = 0·0428). TP53 overexpression is a predictor of poor outcome in patients with MDS-F.

Indexed as

Gene Expression RegulationMutationAdultAgedDisease-Free SurvivalFibrosisHumansMiddle AgedMyelodysplastic SyndromesReticulinSurvival RateTumor Suppressor Protein p53ReticulinTP53 protein, humanTumor Suppressor Protein p53fibrosismyelodysplastic syndromenext-generation sequencingTP53TP53 expression

Identifiers

PMID26123119
PMCPMC5577911
OpenAlexW2144103244

What OpenQuestion holds

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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.