Evidence map›Paper›PMID 41658458›Full record

ArticleTranslational andrology and urology2026

Clinical characteristics and outcomes of relapse in unilateral Wilms tumor: a single-institution report from 2010 to 2022.

Jiangnan Du, Yangyue Huang, Ning Sun, Weiping Zhang, Hongcheng Song, Huanmin Wang

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Article in Translational andrology and urology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Jiangnan Du *Department of Pediatric Urology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Yangyue Huang *Department of Pediatric Urology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Ning SunDepartment of Pediatric Urology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Weiping ZhangDepartment of Pediatric Urology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Hongcheng SongDepartment of Pediatric Urology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Huanmin WangDepartment of Surgical Oncology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Wilms tumor (WT) is the most common pediatric malignant renal tumor in children. Overall, the prognosis for recurrent WT remains poor, with an overall survival (OS) rate of approximately 50%. This study aimed to characterize the clinical features and outcomes of patients with relapsed unilateral WT. Methods: We conducted a retrospective study of patients diagnosed with and treated for relapsed unilateral WT at Beijing Children's Hospital between January 2010 and December 2022. Results: A total of 46 patients with recurrent WT were included in the study. The 5-year event-free survival (EFS) and OS rates from the time of first relapse were 44.5% [95% confidence interval (CI): 28.4-59.4%] and 54.7% (95% CI: 37.4-69.0%), respectively. Multivariable Cox proportional hazards regression analysis revealed that early relapse and nonoperative management after relapse were independent risk factors for a second recurrence. Patients who relapsed within six months had a significantly higher risk of second recurrence than those who relapsed after six months [hazard ratio (HR) 3.0; 95% CI: 1.1-8.8; P=0.03]. Patients who did not undergo surgery after relapse had a significantly higher risk of second recurrence than those who did (HR 3.9; 95% CI: 1.4-11.4; P=0.01). In addition, the only factor significantly associated with OS in this cohort was the histology of the initial tumor. Focal or diffuse anaplasia in the initial tumor was associated with a markedly higher risk of death (HR 10.3; 95% CI: 2.1-50.9; P=0.007). Conclusions: We emphasize the importance of identifying adverse risk factors for recurrent WT. Early relapse (within six months) and nonoperative management after relapse are independent predictors of a second recurrence. Furthermore, unfavorable histology of the initial tumor independently predicts mortality in recurrent WT.

Indexed as

prognosisrelapsetreatmentWilms tumor (WT)

Identifiers

PMID41658458
PMCPMC12877638

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