Evidence map›Paper›PMID 25932436›Full record

ArticleAnnals of laboratory medicine2015

Incidences and Prognostic Impact of c-KIT, WT1, CEBPA, and CBL Mutations, and Mutations Associated With Epigenetic Modification in Core Binding Factor Acute Myeloid Leukemia: A Multicenter Study in a Korean Population.

Sang Hyuk Park, Hyun Ji Lee, In-Suk Kim, Jeong-Eun Kang, Eun Yup Lee, Hyeoung-Joon Kim, Yeo-Kyeoung Kim, Jong-Ho Won, Soo Mee Bang, Hawk Kim and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Annals of laboratory medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Comprehensive Mutation Profile in Acute Myeloid Leukemia Patients withTurkish journal of haematology : official journal of Turkish Society of Haematology · 2022
    Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Functional Properties ofClinical cancer research : an official journal of the American Association for Cancer Research · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. [How I treat acute myeloid leukemia with t (8;21)].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2017
    Article
  15. 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

13 authors at 7 institutions in 1 country.

Sang Hyuk ParkDepartment of Laboratory Medicine, Pusan National University School of Medicine, Pusan National University Hospital, Biomedical Research Institute, Pusan National University Hospital, Busan, Korea.
Hyun Ji LeeDepartment of Laboratory Medicine, Korean Red cross, Changwon, Korea.
In-Suk KimDepartment of Laboratory Medicine, Pusan National University School of Medicine, Pusan National University Yangsan Hospital, Yangsan, Korea.
Jeong-Eun KangDepartment of Laboratory Medicine, Jinhae Yonsei Hospital, Changwon, Korea.
Eun Yup LeeDepartment of Laboratory Medicine, Pusan National University School of Medicine, Pusan National University Hospital, Biomedical Research Institute, Pusan National University Hospital, Busan, Korea.
Hyeoung-Joon KimDepartment of Hematology-Oncology, Chonnam National University Hwasun Hospital, Hwasun, Korea.
Yeo-Kyeoung KimDepartment of Hematology-Oncology, Chonnam National University Hwasun Hospital, Hwasun, Korea.
Jong-Ho WonDepartment of Hematology-Oncology, Soonchunhyang University Hospital, Seoul, Korea.
Soo Mee BangDepartment of Hematology-Oncology, Seoul National University Bundang Hospital, Seongnam, Korea.
Hawk KimDepartment of Hematology-Oncology, Ulsan University Hospital, Ulsan, Korea.
Moo-Kon SongDivision of Hematology-Oncology, Department of Internal Medicine, Pusan National University School of Medicine, Biomedical Research Institute, Pusan National University Hospital, Busan, Korea.
Joo Seop ChungDivision of Hematology-Oncology, Department of Internal Medicine, Pusan National University School of Medicine, Biomedical Research Institute, Pusan National University Hospital, Busan, Korea.
Ho-Jin ShinDivision of Hematology-Oncology, Department of Internal Medicine, Pusan National University School of Medicine, Biomedical Research Institute, Pusan National University Hospital, Busan, Korea.
Pusan National University Hospital · KRUlsan University Hospital · KRChonnam National University Hwasun Hospital · KRKorean Red Cross · KRPusan National University Yangsan Hospital · KRSeoul National University Bundang Hospital · KRSoonchunhyang University Hospital Seoul · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo identify potential molecular prognostic markers in core binding factor (CBF) AML, we analyzed incidences and prognostic impacts of mutations in c-KIT, WT1, CEBPA, CBL, and a number of epigenetic genes in CBF AML.

methodsSeventy one and 21 AML patients with t(8;21) and inv(16) were enrolled in this study, respectively. NPM1, CEBPA, c-KIT, IDH1/2, DNMT3A, EZH2, WT1, and CBL mutations were analyzed by direct sequencing. Patients were categorized with respect to c-KIT and WT1 mutation status, and both clinical features and prognoses were compared.

resultsThe incidences of FLT3 internal tandem duplication (ITD), NPM1, CEBPA, IDH1/2, DNMT3A, EZH2, and CBL mutations were low (≤5%) in CBF AML patients. However, c-KIT and WT1 mutations occurred frequently (10.9% and 13.8%, respectively). t(8;21) patients with c-KIT mutations showed significantly shorter overall survival (OS) and disease free survival (DFS) periods than those without mutations (P<0.001, for both); however, although the limited number of t(8;21) patients were analyzed, WT1 mutation status did not affect prognosis significantly. Relapse or death during follow-up occurred more frequently in t(8;21) patients carrying c-KIT mutations than in those without the mutation, although the difference was significant only in a specific patient subgroup with no WT1 mutations (P=0.014).

conclusionsThe incidences of mutations in epigenetic genes are very low in CBF AML; however, c-KIT and WT1 mutations occur more frequently than others. The poor prognostic impact of c-KIT mutation in t(8;21) AML patients only applies in a specific patient subgroup without WT1 mutations. The prognostic impact of WT1 mutation in CBF AML is not evident and further investigation is required.

Indexed as

AdolescentAdultAgedAged, 80 and overAsian PeopleCCAAT-Enhancer-Binding ProteinsChildCore Binding FactorsDisease-Free SurvivalEpigenesis, GeneticFemaleHumansIncidenceLeukemia, Myeloid, AcuteMaleMiddle AgedCBL protein, humanCCAAT-Enhancer-Binding ProteinsCEBPA protein, humanCore Binding FactorsNPM1 protein, humanNucleophosminProto-Oncogene Proteins c-cblProto-Oncogene Proteins c-kitWT1 protein, humanWT1 ProteinsAcute myeloid leukemiac-KITCore binding factorEpigenetic modificationIncidencePrognosisWT1

Identifiers

PMID25932436
PMCPMC4390696
OpenAlexW2004540353

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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.