Evidence map›Paper›PMID 41368027›Full record

ReviewEJC paediatric oncology2025

Childhood cancer survival in low- and middle-income countries and the Global South: emerging evidence and critical gaps from a scoping review of observational studies.

Marilina Santero, Roberta Ortiz Sequeira, Margarida Cruz Paixao, Maria Muñoz Martinez, Paula Mazorra Roig, Guillermo Chantada, Andres Morales La Madrid, Andre Ilbawi

Abstract readReview
In one paragraph

Review in EJC paediatric oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

8 authors.

Marilina SanteroUniversitat Autònoma Barcelona, Barcelona, Spain.
Roberta Ortiz SequeiraWorld Health Organization, Department of Non-Communicable Diseases, Disability and Rehabilitation, Geneva, Switzerland.
Margarida Cruz PaixaoWorld Health Organization, Department of Non-Communicable Diseases, Disability and Rehabilitation, Geneva, Switzerland.
Maria Muñoz MartinezPediatric Cancer Center Barcelona, Sant Joan de Déu Children's Hospital, Barcelona, Spain.
Paula Mazorra RoigPediatric Cancer Center Barcelona, Sant Joan de Déu Children's Hospital, Barcelona, Spain.
Guillermo ChantadaPediatric Cancer Center Barcelona, Sant Joan de Déu Children's Hospital, Barcelona, Spain.
Andres Morales La MadridPediatric Cancer Center Barcelona, Sant Joan de Déu Children's Hospital, Barcelona, Spain.
Andre IlbawiWorld Health Organization, Department of Non-Communicable Diseases, Disability and Rehabilitation, Geneva, Switzerland.

Funding

World Health Organization 001
6 · The paper itself

Abstract

Background: Survival rates for childhood cancer reveal stark global disparities. While over 80 % of children survive in high-income countries (HICs), outcomes remain significantly lower in low- and middle-income countries (LMICs), where the burden is also higher. This study synthesizes observational data on survival outcomes for the six WHO Global Initiative for Childhood Cancer (GICC) index cancers in LMICs, aiming to establish survival estimates, identify key determinants, and assess data limitations. Methods: Following JBI and PRISMA-ScR guidelines, we conducted a scoping review searching MEDLINE, WHO Global Index Medicus, and EMBASE for observational studies published since 2013. Studies included children aged 0-19 diagnosed with acute lymphoblastic leukemia, Burkitt lymphoma, Hodgkin lymphoma, low-grade glioma, retinoblastoma, or Wilms tumor in LMICs. Results: From 6358 records, 196 studies were included. Most (72.9 %) were retrospective cohorts; 71.9 % were single-institution studies. The most frequently reported cancers were acute lymphoblastic leukemia (35.2 %) and Wilms tumor (29.1 %). Mean reported overall survival varied widely, from 62.5 % for Burkitt lymphoma (range 20.0-92.0 %) to 78.6 % for Hodgkin lymphoma (range 40.0-96.6 %). Median follow-up was often poorly reported. Socioeconomic barriers, limited healthcare access, and diagnostic delays were common determinants of poor outcomes. Only 10 % of studies referenced hospital-based registries, and fewer than 5 % used population-based data, highlighting critical data gaps. Conclusions: This review underscores emerging evidence and persistent limitations in childhood cancer survival data from LMICs. The predominance of single-center, retrospective studies indicates a need for more standardized, collaborative research.

Indexed as

developing countrieshealth disparitiesNeoplasms/epidemiologyobservational studies as topicPediatric oncologysurvival rate

Identifiers

PMID41368027
PMCPMC12682699

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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.