Evidence map›Paper›PMID 41582753›Full record

ArticleZhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics2026

[Clinical characteristics and prognostic analysis of pediatric acute myeloid leukemia with -7/7q- abnormalities].

Fang-Yuan Zheng, Miao Wang, Ming-Ming Ding, Ai-Dong Lu, Yue-Ping Jia, Hui-Min Zeng, Le-Ping Zhang

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Article in Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, 2026. 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.

Fang-Yuan ZhengDepartment of Pediatrics, Peking University People's Hospital, Beijing 100044, China.
Miao WangDepartment of Pediatrics, Peking University People's Hospital, Beijing 100044, China.
Ming-Ming DingDepartment of Pediatrics, Peking University People's Hospital, Beijing 100044, China.
Ai-Dong LuDepartment of Pediatrics, Peking University People's Hospital, Beijing 100044, China.
Yue-Ping JiaDepartment of Pediatrics, Peking University People's Hospital, Beijing 100044, China.
Hui-Min ZengDepartment of Pediatrics, Peking University People's Hospital, Beijing 100044, China.
Le-Ping ZhangDepartment of Pediatrics, Peking University People's Hospital, Beijing 100044, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo explore the clinical characteristics and prognostic factors of pediatric acute myeloid leukemia (AML) with monosomy 7 (-7) and deletion of the long arm of chromosome 7 (7q-).

methodsA retrospective study was conducted on the clinical data, treatment, and prognosis of children with -7/7q- AML who were admitted to the Department of Pediatrics at Peking University People's Hospital from January 2010 to December 2024.

resultsA total of 869 children with AML who had complete karyotype data were included, of whom 32 (3.7%) had -7/7q- chromosomal abnormalities. There were 20 males and 12 females, and the median age at diagnosis was 6 years. Six children (19%) had isolated -7; 2 (6%) had isolated 7q-; and 24 (75%) had additional chromosomal abnormalities. After induction chemotherapy, complete remission (CR) was achieved in 16 children (50%). At the last follow-up, 15 children (47%) had died and 17 (53%) were alive. The 3-year disease-free survival (DFS) rate was (54.1±0.1)%, and the 3-year overall survival (OS) rate was (52.6±0.1)%. The multivariable analysis showed that hematopoietic stem cell transplantation (HSCT) was an independent prognostic factor for DFS (

conclusionsThe incidence of -7/7q- chromosomal abnormalities in children with AML is 3.7%. Additional chromosomal aberrations are common, and the CR rate after induction chemotherapy is low. HSCT is associated with improved prognosis and survival.

Indexed as

Chromosome DeletionChromosomes, Human, Pair 7Leukemia, Myeloid, AcuteAdolescentChildChild, PreschoolChromosome AberrationsFemaleHumansInfantMalePrognosisRetrospective StudiesAcute myeloid leukemiaChildChromosome 7 abnormality

Identifiers

PMID41582753
PMCPMC12833795

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