Evidence map›Paper›PMID 33836835›Full record

ArticleExperimental hematology & oncology2021

Profiling of somatic mutations and fusion genes in acute myeloid leukemia patients with FLT3-ITD or FLT3-TKD mutation at diagnosis reveals distinct evolutionary patterns.

Wei Guan, Lei Zhou, Yan Li, Erna Yang, Yangyang Liu, Na Lv, Lin Fu, Yi Ding, Nan Wang, Nan Fang and 9 more

Open access · goldAbstract read
In one paragraph

Article in Experimental hematology & oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.8field-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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. EJHaem · 2026
    Article
  2. Article
  3. Article
  4. Blood science (Baltimore, Md.) · 2025
    Article
  5. Review
  6. Article
  7. Identification of a novelFrontiers in oncology · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. A Review of FLT3 Kinase Inhibitors in AML.Journal of clinical medicine · 2023
    Review
  12. Article
  13. Review
  14. Case Report: Identification of a novelFrontiers in oncology · 2023
    Article
  15. Review
  16. 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

19 authors at 5 institutions in 1 country.

Wei Guan *Department of Hematology, Chinese PLA General Hospital, 28 Fuxing Road, Beijing, 100853, China.ORCID http://orcid.org/0000-0001-5830-7089
Lei Zhou *Department of Hematology, Chinese PLA General Hospital, 28 Fuxing Road, Beijing, 100853, China.
Yan Li *Department of Hematology, Chinese PLA General Hospital, 28 Fuxing Road, Beijing, 100853, China.
Erna YangDepartment of Hematology and Oncology, Shenzhen Key Laboratory of Precision Medicine for Hematological Malignancies, Carlson International Cancer Center, Shenzhen University General Hospital, Shenzhen University Health Science Center, 1098 Xueyuan AVE, Shenzhen, 518060, China.
Yangyang LiuBeijing USCI Medical Laboratory Co., Ltd, Beijing, China.
Na LvDepartment of Hematology, Chinese PLA General Hospital, 28 Fuxing Road, Beijing, 100853, China.
Lin FuDepartment of Hematology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510260, China.
Yi DingDepartment of Hematology, Chinese PLA General Hospital, 28 Fuxing Road, Beijing, 100853, China.
Nan WangDepartment of Hematology, Chinese PLA General Hospital, 28 Fuxing Road, Beijing, 100853, China.
Nan FangBeijing USCI Medical Laboratory Co., Ltd, Beijing, China.
Qian LiuBeijing USCI Medical Laboratory Co., Ltd, Beijing, China.
Binan WangBeijing USCI Medical Laboratory Co., Ltd, Beijing, China.
Fuwei LiBeijing USCI Medical Laboratory Co., Ltd, Beijing, China.
Juan ZhangBeijing USCI Medical Laboratory Co., Ltd, Beijing, China.
Maoquan WangSchool of Medicine, Nankai University, 94 Weijin Road, Tianjin, 300071, China.
Lili WangDepartment of Hematology, Chinese PLA General Hospital, 28 Fuxing Road, Beijing, 100853, China.
Yu JingDepartment of Hematology, Chinese PLA General Hospital, 28 Fuxing Road, Beijing, 100853, China.
Yonghui LiDepartment of Hematology and Oncology, Shenzhen Key Laboratory of Precision Medicine for Hematological Malignancies, Carlson International Cancer Center, Shenzhen University General Hospital, Shenzhen University Health Science Center, 1098 Xueyuan AVE, Shenzhen, 518060, China.
Li YuDepartment of Hematology, Chinese PLA General Hospital, 28 Fuxing Road, Beijing, 100853, China. liyu301@vip.163.com.ORCID http://orcid.org/0000-0001-6872-2665
Chinese PLA General Hospital · CNPeking University · CNNankai University · CNSecond Affiliated Hospital of Guangzhou Medical University · CNShenzhen University Health Science Center · CN

Funding

Beijing Natural Science Foundation 7202186Major science and technology projects for major new drug creation 2019ZX09201-002National Natural Science Foundation of China 81570137National Natural Science Foundation of China 81870134the National Natural Science Foundation of China 81670162the National Natural Science Foundation of China 81800135
6 · The paper itself

Abstract

backgroundThe receptor tyrosine kinase FLT3 with internal tandem duplications within the juxtamembrane domain (FLT3-ITD) is a poor prognostic factor; however, the prognostic significance of missense mutation in the tyrosine kinase domain (FLT3-TKD) is controversial. Furthermore, the accompanying mutations and fusion genes with FLT3 mutations are unclear in acute myeloid leukemia (AML).

methodsWe investigated FLT3 mutations and their correlation with other gene mutations and gene fusions through two RNA-seq based next-generation sequencing (NGS) method and prognostic impact in 207 de novo AML patients.

resultsFLT3-ITD mutations were positive in 58 patients (28%), and FLT3-TKD mutations were positive in 20 patients (9.7%). FLT3-ITD was associated with a higher white blood cell count (WBC, mean 72.9 × 10

conclusionsOur study offers deep insights into the molecular pathogenesis and biology of AML with FLT3-ITD and FLT3-TKD by providing the profiles of concurrent molecular alterations and the clinical impact of FLT3-ITD and FLT3-TKD on AML patients.

Indexed as

Acute myeloid leukemiaFLT3-ITDFLT3-TKDNext-generation sequencingTET2

Identifiers

PMID33836835
PMCPMC8033687
OpenAlexW3148385210

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.