Evidence map›Paper›PMID 36864435›Full record

ArticleBMC cancer2023

One year overall survival of wilms tumor cases and its predictors, among children diagnosed at a teaching hospital in South Western Uganda: a retrospective cohort study.

Eddymond Ekuk, Charles Newton Odongo, Leevan Tibaijuka, Felix Oyania, Walufu Ivan Egesa, Felix Bongomin, Raymond Atwiine, Moses Acan, Martin Situma

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Bacteria in neoplastic diseases: A brief note on Wilms tumor.World journal of experimental medicine · 2025
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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

9 authors at 4 institutions in 1 country.

Eddymond EkukDepartment of Surgery, Mbarara University of Science and Technology, Faculty of Medicine, Mbarara, Uganda. eddiemakori@yahoo.com.
Charles Newton OdongoDepartment of Surgery, Mbarara University of Science and Technology, Faculty of Medicine, Mbarara, Uganda.
Leevan TibaijukaDepartment of Surgery, Mbarara University of Science and Technology, Faculty of Medicine, Mbarara, Uganda.
Felix OyaniaDepartment of Surgery, Mbarara University of Science and Technology, Faculty of Medicine, Mbarara, Uganda.
Walufu Ivan EgesaDepartment of Pediatrics, Faculty of Clinical Medicine and Dentistry, Kampala International, Kampala, Uganda.
Felix BongominDepartment of Microbiology, Mycology, and Immunology, Internal Medicine Gulu University, Gulu, Uganda.
Raymond AtwiineDepartment of Surgery, Mbarara University of Science and Technology, Faculty of Medicine, Mbarara, Uganda.
Moses AcanDepartment of Surgery, Mbarara University of Science and Technology, Faculty of Medicine, Mbarara, Uganda.
Martin SitumaDepartment of Surgery, Mbarara University of Science and Technology, Faculty of Medicine, Mbarara, Uganda.
Mbarara University of Science and Technology · UGGulu University · UGKampala International University · UGSoroti University · UG

Funding

Multi-morbidity in Uganda Research Capacity Initiative (MURCI) at Mbarara University of Science and TechnologyD43TW011632 · FIC · MBARARA UNIVERSITY/SCIENCE/ TECHNOLOGY · PI BAJUNIRWE, FRANCIS · 2020 to 2024
$1.2M
FIC NIH HHS D43 TW011632
6 · The paper itself

Abstract

backgroundWilms tumor (WT) is the second most common solid tumor in Africa with both low overall survival (OS) and event-free survival (EFS) rates. However, no known factors are predicting this poor overall survival.

objectiveThe study was to determine the one-year overall survival of WT cases and its predictors among children diagnosed in the pediatric oncology and surgical units of Mbarara regional referral hospital (MRRH), western Uganda. METHODOLOGY: Children's treatment charts and files diagnosed and managed for WT were retrospectively followed up for the period between January 2017 to January 2021. Charts of children with histologically confirmed diagnoses were reviewed for demographics, clinical and histological characteristics, as well as treatment modalities.

resultsOne-year overall survival was found to be 59.3% (95% CI: 40.7-73.3), with tumor size greater than 15 cm (p 0.021) and unfavorable WT type (p 0.012) being the predominant predictors.

conclusionOverall survival (OS) of WT at MRRH was found to be 59.3%, and predictive factors noted were unfavorable histology and tumor size greater than 115 cm.

Indexed as

Kidney NeoplasmsNeoplasms, Second PrimaryWilms TumorChildHospitals, TeachingHumansRetrospective StudiesUgandaEvent-free survivalHistology characteristicsOverall survivalPredictors of survivalWilms tumor

Identifiers

PMID36864435
PMCPMC9979450
OpenAlexW4322773507

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.