Evidence map›Paper›PMID 38146893›Full record

ArticleCancer medicine2024

Prognosis and risk factors for ASXL1 mutations in patients with newly diagnosed acute myeloid leukemia and myelodysplastic syndrome.

Liqing Yang, Xiaoyu Wei, Yuping Gong

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. [Clinical characteristics of RUNX1-mutated acute myeloid leukemia patients].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. African journal of laboratory medicine · 2026
    Article
  8. Article
  9. Epigenetic alterations in Myeloid Malignancies.Advances in experimental medicine and biology · 2026
    Review
  10. Review
  11. Review
  12. Article
  13. 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

3 authors at 2 institutions in 1 country.

Liqing YangDepartment of Hematology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.ORCID 0000-0003-2646-4359
Xiaoyu WeiDepartment of Hematology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Yuping GongDepartment of Hematology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.ORCID 0000-0002-2437-9348
Sichuan University · CNFujian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe objective of the study was to determine the prognosis and risk factors for additional sex combs like 1 (ASXL1) mutations in patients with acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS). POPULATION AND

methodsThis retrospective study enrolled 219 adult patients with newly diagnosed AML and MDS, who were treated in West China Hospital from October 2018 to January 2022. The primary clinical outcome was evaluated by overall survival (OS) followed up to January 2023. Kaplan-Meier analysis and Cox multivariate regression analysis were performed to identify potential prognostic parameters in patients with ASXL1 mutations (mt).

resultsA total of 34 (15.53%) ASXL1

conclusionOur study indicated that mutations in G646W or RUNX1 co-mutations are closely associated with a dismal clinical outcome in patients with AML and MDS harboring ASXL1

Indexed as

Leukemia, Myeloid, AcuteMutationMyelodysplastic SyndromesRepressor ProteinsAdolescentAdultAgedAged, 80 and overCore Binding Factor Alpha 2 SubunitFemaleHumansKaplan-Meier EstimateMaleMiddle AgedPrognosisRetrospective StudiesASXL1 protein, humanCore Binding Factor Alpha 2 SubunitRepressor ProteinsRUNX1 protein, humanacute myeloid leukemiaadditional sex combs like 1 (ASXL1)myelodysplastic syndromeprognosisrisk factor

Identifiers

PMID38146893
PMCPMC10807681
OpenAlexW4390229696

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.