Evidence map›Paper›PMID 41351026›Full record

ArticleEuropean journal of medical research2025

The impact of asparaginase phenotype-related single nucleotide polymorphisms on prognosis in pediatric B-cell precursor acute lymphoblastic leukemia.

Jingying Zhang, Caiting Xu, Jiayue Qin, Diying Shen, Lixia Liu, Tian Xia, Xiaojun Xu

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Article in European journal of medical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Jingying Zhang *Division/Center of Pediatric Hematology-Oncology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310005, China.
Caiting Xu *Division/Center of Pediatric Hematology-Oncology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310005, China.
Jiayue Qin *Department of Medical Affairs, Acornmed Biotechnology Co., Ltd, Beijing, 100176, China.
Diying ShenDivision/Center of Pediatric Hematology-Oncology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310005, China.
Lixia LiuDepartment of Medical Affairs, Acornmed Biotechnology Co., Ltd, Beijing, 100176, China.
Tian XiaDivision/Center of Pediatric Hematology-Oncology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310005, China.
Xiaojun XuDivision/Center of Pediatric Hematology-Oncology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310005, China. xuxiaojun@zju.edu.cn.

Funding

Natural Science Foundation of Zhejiang Province, China LY24H080002Zhejiang Province Medical and Health Science and Technology Project No. 2024657646
6 · The paper itself

Abstract

backgroundPediatric B-cell precursor acute lymphoblastic leukemia (BCP-ALL) is a significant hematological malignancy and asparaginase plays a significant role in the treatment of BCP-ALL. However, the prognostic value of asparaginase phenotype-related single nucleotide polymorphisms (SNPs) in BCP-ALL remains unclear.

methodsHere, we examined clinical characteristics, genetic mutations, asparaginase phenotype-related SNPs (ADSL (793-49A > C), NFATC2 (2722 + 12367 T > A), PNPLA3 (444C > G), and SOD2 (47A > G)) and treatment outcomes in a retrospective cohort of 356 newly diagnosed BCP-ALL patients.

resultsKaplan-Meier survival analysis of relapse-free survival (RFS) identified five significant risk factors: age ≥ 10 years, white blood cell count ≥ 50 × 10

conclusionsThese findings underscore the importance of asparaginase phenotype-related SNP, ADSL (793-49A > C), in personalized treatment strategies based on genetic profiling and clinical parameters, potentially enhancing therapeutic efficacy and patient outcomes in pediatric BCP-ALL.

Indexed as

AsparaginasePolymorphism, Single NucleotidePrecursor B-Cell Lymphoblastic Leukemia-LymphomaAdolescentChildChild, PreschoolFemaleHumansInfantMaleMutationPhenotypePrognosisRetrospective StudiesAsparaginaseAsparaginaseBCP-ALLRFSSNP

Identifiers

PMID41351026
PMCPMC12681128

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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.