Evidence map›Paper›PMID 28070990›Full record

ArticleCancer medicine2017

A targeted next-generation sequencing in the molecular risk stratification of adult acute myeloid leukemia: implications for clinical practice.

Po-Han Lin, Huei-Ying Li, Sheng-Chih Fan, Tzu-Hang Yuan, Ming Chen, Yu-Hua Hsu, Yu-Hsuan Yang, Long-Yuan Li, Su-Peng Yeh, Li-Yuan Bai and 9 more

Abstract read
In one paragraph

Article in Cancer medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

29 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
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  14. Observational
  15. Clinico-pathologic characteristics and outcomes of the World Health Organization (WHO) provisional entity de novo acute myeloid leukemia with mutated RUNX1.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2020
    Article
  16. Review
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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.

Po-Han LinDepartment of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.
Huei-Ying LiDepartment of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.
Sheng-Chih FanDepartment of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.
Tzu-Hang YuanDepartment of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.
Ming ChenDepartment of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.
Yu-Hua HsuDepartment of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.
Yu-Hsuan YangDepartment of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.
Long-Yuan LiDepartment of Life Sciences, National Chung Hsing University, Taichung, 40227, Taiwan.
Su-Peng YehDivision of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital.
Li-Yuan BaiDivision of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital.
Yu-Min LiaoDivision of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital.
Chen-Yuan LinDivision of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital.
Ching-Yun HsiehDivision of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital.
Ching-Chan LinDivision of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital.
Che-Hung LinDivision of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital.
Ming-Yu LienDivision of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital.
Tzu-Ting ChenDivision of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital.
Yen-Hsuan NiDepartment of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.
Chang-Fang ChiuDivision of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Conventional cytogenetics can categorize patients with acute myeloid leukemia (AML) into favorable, intermediate, and unfavorable-risk groups; however, patients with intermediate-risk cytogenetics represent the major population with variable outcomes. Because molecular profiling can assist with AML prognosis and next-generation sequencing allows simultaneous sequencing of many target genes, we analyzed 260 genes in 112 patients with de novo AML who received standard treatment. Multivariate analysis showed that karyotypes and mutation status of TET2, PHF6, KIT, and NPM1

Indexed as

Genetic Predisposition to DiseaseMutationAdolescentAdultAgedChildCytogenetic AnalysisFemaleGene Regulatory NetworksHigh-Throughput Nucleotide SequencingHumansLeukemia, Myeloid, AcuteMaleMiddle AgedNucleophosminPrognosisNucleophosminAcute myeloid leukemiagene mutationsnext-generation sequencingprecision medicineprognosis

Identifiers

PMID28070990
PMCPMC5313641

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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 OpenQuestion graph.