Evidence map›Paper›PMID 41430658›Full record

ArticleBMC pediatrics2025

Clinical characteristics and survival outcomes of surgically managed prenatally diagnosed neuroblastoma: a single-center, real-world study.

Kongkong Cui, Peng Hong, Zaihong Hu, Jie Lin, Zhiqiang Gao, Honggang Fang, Xiaomao Tian, Qinlin Shi, Guanghui Wei

Abstract read
In one paragraph

Article in BMC pediatrics, 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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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Kongkong CuiDepartment of Urology Children's Hospital of Chongqing Medical University, National Clinical Research Center for Children and Adolescents' Health and Diseases, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing, China.
Peng HongDepartment of Urology Children's Hospital of Chongqing Medical University, National Clinical Research Center for Children and Adolescents' Health and Diseases, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing, China.
Zaihong HuDepartment of Urology Children's Hospital of Chongqing Medical University, National Clinical Research Center for Children and Adolescents' Health and Diseases, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing, China.
Jie LinDepartment of Urology Children's Hospital of Chongqing Medical University, National Clinical Research Center for Children and Adolescents' Health and Diseases, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing, China.
Zhiqiang GaoDepartment of Urology Children's Hospital of Chongqing Medical University, National Clinical Research Center for Children and Adolescents' Health and Diseases, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing, China.
Honggang FangDepartment of Urology Children's Hospital of Chongqing Medical University, National Clinical Research Center for Children and Adolescents' Health and Diseases, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing, China.
Xiaomao TianDepartment of Urology Children's Hospital of Chongqing Medical University, National Clinical Research Center for Children and Adolescents' Health and Diseases, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing, China.
Qinlin ShiDepartment of Urology Children's Hospital of Chongqing Medical University, National Clinical Research Center for Children and Adolescents' Health and Diseases, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing, China. 485141@hospital.cqmu.edu.cn.
Guanghui WeiDepartment of Urology Children's Hospital of Chongqing Medical University, National Clinical Research Center for Children and Adolescents' Health and Diseases, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing, China.

Funding

China Postdoctoral Science Foundation 2022M720609National Natural Science Foundation of China 82302948
6 · The paper itself

Abstract

backgroundWith the advancement of ultrasound technology, prenatally diagnosed neuroblastoma (PNB) has become increasingly common. However, knowledge of this particular case remains limited and is usually confined to individual case reports. There is still a lack of research on the clinical characteristics, treatment-related complications, long-term abnormal health problems and quality of life (QoL) of patients with PNB.

methodsThis retrospective study included 49 patients with PNB treated at a tertiary center between 2012 and 2025 and 102 cases from 32 prior studies (total n = 151). Collected data encompassed demographics, tumor characteristics, treatment methods, complications, and survival outcomes. And conduct follow-up evaluations on the patient’s treatment outcome, long-term health status, and QoL.

resultsPNB originated predominantly in the adrenal glands (83.7%), with 63.3% classified as low-risk. Metastasis occurred in 30.6% of cases, primarily involving the liver (80%). MYCN amplification was rare (6.1%), and elevated 24-hour urinary vanillylmandelic acid (VMA) levels were present in only 10.2% of cases. Five-year overall survival (OS) and event-free survival (EFS) rates reached 93.3% and 86.8%, respectively. Survivors had few long-term health problems and QoL scores were comparable to those of healthy children. A comprehensive analysis of 151 patients showed a survival rate of 93.4%, further confirming that PNB has a favorable prognosis.

conclusionThis study is the largest retrospective cohort analysis of PNB to date. It systematically summarizes the clinical characteristics of PNB patients and demonstrates their favorable prognosis and QoL. Furthermore, the findings provide critical evidence to guide risk-stratified management and prenatal counseling.

Indexed as

Adrenal Gland NeoplasmsNeuroblastomaChild, PreschoolFemaleHumansInfantInfant, NewbornMalePregnancyPrenatal DiagnosisQuality of LifeRetrospective StudiesSurvival RateTreatment OutcomeVanilmandelic AcidVanilmandelic AcidAntenatal ultrasoundNeuroblastomaOutcomePrognosis

Identifiers

PMID41430658
PMCPMC12869947

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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.