Evidence map›Paper›PMID 39533245›Full record

ArticleBMC cancer2024

The outcomes of children with primary malignant renal tumors: a 14-year single-center experience.

Shayan Bordbar, Mahdi Shahriari, Omid Reza Zekavat, Hadi Mottaghipisheh, Sezaneh Haghpanah, Mohammadreza Bordbar

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Article in BMC cancer, 2024. 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

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Shayan BordbarStudent Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.
Mahdi ShahriariHematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Omid Reza ZekavatHematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Hadi MottaghipishehHematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Sezaneh HaghpanahHematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Mohammadreza BordbarHematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. mbordbar53@gmail.com.

Funding

Shiraz University of Medical Sciences 28659
6 · The paper itself

Abstract

backgroundWilms tumor (WT) is the most common malignant renal tumor in children. This study investigated the clinical features, pathological findings, and outcomes of children with malignant renal tumors in Southern Iran. Factors associated with recurrence and mortality were assessed.

methodsElectronic files of children with malignant renal tumors from 2009 to 2023 were reviewed. The 5-year overall survival (OS) and event-free survival (EFS) were reported.

resultsEighty-three patients (44 males) with a median age of 40 months (range: 3-122) were included. WT was the most common pathological variant (94%). Anaplasia was found in 17.3% of patients. Upfront chemotherapy followed by nephrectomy was performed in 54.2% of the patients. Ten patients (12%) experienced relapse, and five patients (6%) died during the 14-year follow-up. The 5-year OS and EFS were 90.75% (95% CI, 78.64-96.16%) and 81.9% (95% CI, 70.10-89.38%), respectively, and were comparable between the two treatment strategies (upfront chemotherapy vs. upfront nephrectomy). Metastasis and residual disease were associated with relapse, whereas tumor recurrence was the only predictive factor of survival.

conclusionWT is a curable disease with excellent outcomes if diagnosed and treated promptly. The timing of nephrectomy does not affect OS and EFS. Patients with low-stage tumors and those with complete surgical excision are at a lower risk of tumor recurrence. Relapse is the primary risk factor for death.

Indexed as

Kidney NeoplasmsNeoplasm Recurrence, LocalNephrectomyAdolescentChildChild, PreschoolFemaleFollow-Up StudiesHumansInfantIranMalePrognosisRetrospective StudiesTreatment OutcomeWilms TumorRelapseRisk factorsSurvivalTreatmentWilms tumor

Identifiers

PMID39533245
PMCPMC11555868

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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.