Evidence map›Paper›PMID 38594285›Full record

ArticleBlood cancer journal2024

Comparison of the 2022 world health organization classification and international consensus classification in myelodysplastic syndromes/neoplasms.

Wan-Hsuan Lee, Chien-Chin Lin, Xavier Cheng-Hong Tsai, Feng-Ming Tien, Min-Yen Lo, Mei-Hsuan Tseng, Yuan-Yeh Kuo, Shan-Chi Yu, Ming-Chih Liu, Chang-Tsu Yuan and 9 more

Open access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
10.5field-weighted citation impact, top 1% 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

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

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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 at 4 institutions in 1 country.

Wan-Hsuan LeeDivisions of Hematology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Chien-Chin LinDivisions of Hematology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Xavier Cheng-Hong TsaiDivisions of Hematology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Feng-Ming TienDivisions of Hematology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.ORCID http://orcid.org/0000-0003-4513-2472
Min-Yen LoDivisions of Hematology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Mei-Hsuan TsengTai-Chen Cell Therapy Center, National Taiwan University, Taipei, Taiwan.
Yuan-Yeh KuoTai-Chen Cell Therapy Center, National Taiwan University, Taipei, Taiwan.ORCID http://orcid.org/0000-0002-6090-9000
Shan-Chi YuDepartment of Pathology, National Taiwan University Hospital, Taipei, Taiwan.
Ming-Chih LiuDepartment of Pathology, National Taiwan University Hospital, Taipei, Taiwan.
Chang-Tsu YuanGraduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.
Yi-Tsung YangDivisions of Hematology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Ming-Kai ChuangDivisions of Hematology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Bor-Sheng KoDivisions of Hematology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan. bskomd@ntu.edu.tw.
Jih-Luh TangDivisions of Hematology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Hsun-I SunTai-Chen Cell Therapy Center, National Taiwan University, Taipei, Taiwan.
Yi-Kuang ChuangTai-Chen Cell Therapy Center, National Taiwan University, Taipei, Taiwan.
Hwei-Fang TienDivisions of Hematology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.ORCID http://orcid.org/0000-0002-1384-5593
Hsin-An HouDivisions of Hematology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan. hsinanhou@ntu.edu.tw.ORCID http://orcid.org/0000-0003-2780-4845
Wen-Chien ChouDivisions of Hematology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.ORCID http://orcid.org/0000-0003-2967-698X
National Taiwan University · TWNational Taiwan University Hospital · TWFar Eastern Memorial Hospital · TWNational Taitung University · TW

Funding

Ministry of Science and Technology, Taiwan (Ministry of Science and Technology of Taiwan) 106-2314-B-002-226-MY3Ministry of Science and Technology, Taiwan (Ministry of Science and Technology of Taiwan) 108-2628-B-002-015Ministry of Science and Technology, Taiwan (Ministry of Science and Technology of Taiwan) 109-2314-B-002-213
6 · The paper itself

Abstract

In 2022, two novel classification systems for myelodysplastic syndromes/neoplasms (MDS) have been proposed: the International Consensus Classification (ICC) and the 2022 World Health Organization (WHO-2022) classification. These two contemporary systems exhibit numerous shared features but also diverge significantly in terminology and the definition of new entities. Thus, we retrospectively validated the ICC and WHO-2022 classification and found that both systems promoted efficient segregation of this heterogeneous disease. After examining the distinction between the two systems, we showed that a peripheral blood blast percentage ≥ 5% indicates adverse survival. Identifying MDS/acute myeloid leukemia with MDS-related gene mutations or cytogenetic abnormalities helps differentiate survival outcomes. In MDS, not otherwise specified patients, those diagnosed with hypoplastic MDS and single lineage dysplasia displayed a trend of superior survival compared to other low-risk MDS patients. Furthermore, the impact of bone marrow fibrosis on survival was less pronounced within the ICC framework. Allogeneic transplantation appears to improve outcomes for patients diagnosed with MDS with excess blasts in the ICC. Therefore, we proposed an integrated system that may lead to the accurate diagnosis and advancement of future research for MDS. Prospective studies are warranted to validate this refined classification.

Indexed as

Myelodysplastic SyndromesNeoplasmsConsensus Statements as TopicHumansPrognosisRetrospective StudiesWorld Health Organization

Identifiers

PMID38594285
PMCPMC11004131
OpenAlexW4394613085

What OpenQuestion holds

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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.