Evidence map›Paper›PMID 35933338›Full record

ArticleBMC cancer2022

Poor treatment responses were related to poor outcomes in pediatric B cell acute lymphoblastic leukemia with KMT2A rearrangements.

Jinquan Wen, Min Zhou, Yali Shen, Yueting Long, Yuxia Guo, Lin Song, Jianwen Xiao

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
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  4. Updates inBiomedicines · 2023
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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

7 authors at 5 institutions in 1 country.

Jinquan WenDepartment of Pediatric Hematology, Caihong Hospital of Xianyang, Xi'an, People's Republic of China.
Min Zhou *Department of Hematology, Chengdu Women and Children's Central Hospital, Chengdu, People's Republic of China.
Yali Shen *Department of Hematology, Children's Hospital of Chongqing Medical University, Yuzhong District, Zhongshan 2nd Road, Chongqing, 400014, People's Republic of China.
Yueting LongDepartment of Pediatrics, The Second Affiliated Hospital of Guizhou Medical University, Kaili, People's Republic of China.
Yuxia GuoDepartment of Hematology, Children's Hospital of Chongqing Medical University, Yuzhong District, Zhongshan 2nd Road, Chongqing, 400014, People's Republic of China.
Lin SongDepartment of Pharmacy, Children's Hospital of Chongqing Medical University, Chongqing, People's Republic of China.
Jianwen XiaoDepartment of Hematology, Children's Hospital of Chongqing Medical University, Yuzhong District, Zhongshan 2nd Road, Chongqing, 400014, People's Republic of China. tomahawk6502@sohu.com.
Children's Hospital of Chongqing Medical University · CNAffiliated Hospital of Guizhou Medical University · CNChengdu Women's and Children's Central Hospital · CNChina International Science and Technology Cooperation · CNChongqing Medical University · CN

Funding

Chongqing Science and Technology Commission of China cstc2018jsyj-jsyjX0015National Natural Science Foundation of China 81900162
6 · The paper itself

Abstract

backgroundThe KMT2A gene, formerly named the MLL gene, is rearranged (KMT2Ar) in 70-75% of infants, 5-6% of children and 10-15% of adult patients with B cell acute lymphoblastic leukemia (B-ALL). The outcome after chemotherapy of pediatric cases remains poor, and only a few studies have investigated the clinical and laboratory features, treatment response and prognosis in Chinese populations.

methodsA total of 48 B-ALL children with KMT2Ar were enrolled in the study, and clinical and laboratory data were collected and analyzed by age group. The relationship between prognosis and traditional risk factors and treatment response was investigated for these patients who received chemotherapy.

resultsThe 48 enrolled patients included 28 males and 20 females; 18 (37.50%) or 30 (62.50%) patients were an age of < 12 m (infant B-ALL) or of > 12 m at onset. An initial WBC count of 300 × 10

Indexed as

Burkitt LymphomaPrecursor Cell Lymphoblastic Leukemia-LymphomaChildFemaleHumansMaleNeoplasm, ResidualPrognosisProspective StudiesRemission InductionB cell acute lymphoblastic leukemiaKMT2A rearrangementMinimal residual diseasePediatricPrognosisTreatment response

Identifiers

PMID35933338
PMCPMC9357304
OpenAlexW4290068932

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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.