Evidence map›Paper›PMID 42755603›Full record

ArticleFrontiers in oncology2026

Treatment and outcomes of hepatoblastoma in a tertiary care pediatric institution: a single-center experience.

Aleksandar Sretenović, Srđa Janković, Nada Krstovski, Polina Pavićević, Jelena Lazić, Goran Milošević, Marija Ćazić, Jelena Krcunović, Branislav Jovanović, Tijana Radović and 7 more

Abstract read
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Article in Frontiers in oncology, 2026. 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

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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

17 authors.

Aleksandar SretenovićFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Srđa JankovićDepartment of Immunology, University Children's Hospital, Belgrade, Serbia.
Nada KrstovskiFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Polina PavićevićFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Jelena LazićFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Goran MiloševićFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Marija ĆazićDepartment of Immunology, University Children's Hospital, Belgrade, Serbia.
Jelena KrcunovićDepartment of Hematology And Oncology, University Children's Hospital, Belgrade, Serbia.
Branislav JovanovićFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Tijana RadovićFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Đorđe PavlovićDepartment of Abdominal Surgery, University Children's Hospital, Belgrade, Serbia.
Dubravka MilutinovićDepartment of Radiology, University Children's Hospital, Belgrade, Serbia.
Jelena Pejanović JovanovićFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Ivana DašićDepartment of Radiology, University Children's Hospital, Belgrade, Serbia.
Sofija CvejićDepartment of Radiology, University Children's Hospital, Belgrade, Serbia.
Jovana Svorcan PavlovićDepartment of Hematology And Oncology, University Children's Hospital, Belgrade, Serbia.
Predrag RodićFaculty of Medicine, University of Belgrade, Belgrade, Serbia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Hepatoblastoma is the most prevalent pediatric malignant liver neoplasm, and despite substantial advances in multimodal treatment, outcome data from Southeast European pediatric centers remain limited. The aim of this study was to evaluate the clinical characteristics, treatment approaches, surgical management, and outcomes of children treated for hepatoblastoma at a tertiary pediatric institution over a 17-year period. Methods: This retrospective single-center cohort study included 24 pediatric patients treated between January 2008 and March 2025. Clinical variables included age, sex, tumor size, PRETEXT stage, metastatic disease, and vascular involvement. Treatment variables comprised chemotherapy protocol, surgical procedure, liver transplantation, and resection margin status, while outcome measures included relapse, overall survival, and normalization of serum α-fetoprotein levels. Results: With the exception of one child who died before treatment could be initiated, all patients underwent surgical treatment following liver biopsy and preoperative chemotherapy. Overall, six children (25.0%) died, whereas 18 were alive at the time of analysis, corresponding to an overall survival rate of 75.0% with a median follow-up of 9.0 years. All patients with PRETEXT 1 and PRETEXT 2 disease survived, whereas survival among patients with PRETEXT 3-4 disease was significantly lower (100.0% vs. 50.0%, p = 0.014). Postoperative relapse occurred in two of the 23 treated patients (8.7%), and serum α-fetoprotein levels normalized after treatment in all surviving patients. Discussion: In this retrospective single-center cohort, multimodal treatment of hepatoblastoma achieved an overall survival of 75.0%, with particularly favorable outcomes in patients with PRETEXT 1-2 disease and negative surgical margins. These findings provide valuable long-term real-world evidence on hepatoblastoma management at a tertiary pediatric referral center.

Indexed as

hepatoblastomaliver resectionpediatric liver tumorspretexttreatment outcome

Identifiers

PMID42755603
PMCPMC13581549

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