Evidence map›Paper›PMID 23845613›Full record

ArticleJournal of pediatric surgery2013

Imaging analysis of hepatoblastoma resectability across neoadjuvant chemotherapy.

Andrew J Murphy, Gregory D Ayers, Melissa A Hilmes, Kaushik Mukherjee, Kevin J Wilson, Wade M Allen, Israel Fernandez-Pineda, Myrick C Shinall, Zhiguo Zhao, Wayne L Furman and 3 more

Abstract readEvaluation Study
In one paragraph

Article in Journal of pediatric surgery, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–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

11 citing papers in PubMed.

  1. Hepatoblastoma.Nature reviews. Disease primers · 2025
    Review
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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

13 authors.

Andrew J MurphyDepartment of Pediatric Surgery, Vanderbilt University Medical Center, Nashville, TN 37232-2730, USA. andrew.j.murphy@vanderbilt.edu
Gregory D Ayers
Melissa A Hilmes
Kaushik Mukherjee
Kevin J Wilson
Wade M Allen
Israel Fernandez-Pineda
Myrick C Shinall
Zhiguo Zhao
Wayne L Furman
Mary Beth McCarville
Andrew M Davidoff
Harold N Lovvorn

Funding

VANDERBILT UNIVERSITY CTSA FOR PEDIATRIC RESEARCHUL1RR024975 · NCRR · VANDERBILT UNIVERSITY · PI BERNARD, GORDON RAPHAEL · 2007 to 2011
$45.7M
Surgical Oncology Training GrantT32CA106183 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI James Richard Goldenring · 2004 to 2026
$6.0M
CITED1 nuclear localization and its role in Wilms' tumor pathogenesisR00CA135695 · NCI · VANDERBILT UNIVERSITY · PI LOVVORN, HAROLD NEWTON · 2010 to 2012
$732k
NCI NIH HHS 4R00CA135695-03NCI NIH HHS 5T32CA106183-06A1NCI NIH HHS R00 CA135695NCI NIH HHS T32 CA106183NCRR NIH HHS 1 UL1 RR024975NCRR NIH HHS UL1 RR024975PHS HHS 21766
6 · The paper itself

Abstract

purposeHepatoblastomas often require neoadjuvant chemotherapy to facilitate partial hepatectomy, which necessitates freedom of tumor borders from the confluence of hepatic veins (COHV), portal vein bifurcation (PVB), and retrohepatic inferior vena cava (IVC). This study aimed to clarify the effect of incremental neoadjuvant cycles on the AHEP0731 protocol criteria of hepatoblastoma resectability.

methodsHepatoblastoma responses to neoadjuvant chemotherapy were analyzed among patients (n=23) treated at two children's hospitals between 1996 and 2010. Using digital imaging data, ellipsoid and point-based models were created to measure tumor volume regression and respective distances from tumor borders nearest to the COHV, PVB, and IVC.

resultsHepatoblastoma volumes regressed with incremental neoadjuvant chemotherapy cycles (p<0.001). Although tumor borders regressed away from the COHV (p=0.008), on average only 1.1mm was gained. No change from tumor borders to the PVB was detected (p=0.102). Distances from tumor borders to the IVC remained stable at one hospital (p=0.612), but increased only 0.15 mm every 10 days of therapy at the other (p=0.002). Neoadjuvant chemotherapy induced slightly more tumors to meet the threshold vascular margin of 1cm (baseline to completion): COHV, 11 (47.8%) to 17 (73.9%; p=0.058); PVB, 11 (47.8%) to 15 (65.2%; p=0.157); and IVC, 4 (17.4%) to 10 (43.5%; p=0.034). No differences were detected in demographic or disease-specific characteristics between patients who did or did not achieve this 1-cm margin after conclusion of chemotherapy.

conclusionHepatoblastoma volumes regress significantly with increasing neoadjuvant chemotherapy cycles. However, tumors often remain anchored to the major hepatic vasculature, showing marginal improvement in resectability criteria.

Indexed as

HepatectomyMagnetic Resonance ImagingTomography, X-Ray ComputedAlgorithmsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsChemotherapy, AdjuvantCisplatinClinical ProtocolsDoxorubicinFemaleFluorouracilHepatoblastomaHumansImage Interpretation, Computer-AssistedLiver NeoplasmsAntineoplastic AgentsCisplatinDoxorubicinFluorouracilVincristineAHEP0731HepatoblastomaNeoadjuvant chemotherapyTumor regressionTumor volume

Identifiers

PMID23845613
PMCPMC3735614

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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.